27 Healthcare Project Management jobs in Pakistan
Clinical Trials Quality Assurance Associate (Night)
Posted 10 days ago
Job Viewed
Job Description
JOB DESCRIPTION:
Minerva Research Solutions is a clinical trial management service provider.We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle.
Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines & real-time solutions. Our clinical trial support services & consultations are tailored to foster your product and requirements.
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.
Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data.
Responsibilities:
- Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness.
- Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations.
- Perform quality control checks; identify and track source documentation errors and non-conformances with requirements.
- Provide ongoing compliance support including but not limited to:
- Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans.
- Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs).
- Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities.
- Assist in preparing for all Sponsor and FDA audits.
- Assist in conducting internal audits to review key processes.
- Provide appropriate support to assigned cross-functional workgroups.
- Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement.
- Query resolution and data entry and questionnaire preparation regarding the respective studies.
- Other related Quality Assurance projects as assigned.
- The QA Associate will report to the Quality Assurance Lead
Knowledge, Education, and Experience:
- Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc)with a keen interest in Clinical Research are strongly encouraged to apply.
- In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials.
- Knowledge of IRB requirements.
- 1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred.
- Experience including external clinical/regulatory and document auditing will be a plus
Skills and Abilities:
- Good communication skills (interpersonal, written, verbal)
- Strong attention to detail and good time management skills
- Flexible attitude concerning work assignments
- Ability to manage multiple and varied tasks in a fast-moving environment
- Ability to interact professionally at all levels within the organization.
- Knowledge of the HIPAA Privacy Act and its application to clinical research.
- Competitive salary and performance-based bonuses.
- Medical health insurance coverage.
- Employees Old-age benefits coverage.
- Flexible work hours and remote work options.
- Professional learning and developmentsupport.
- Generous vacation and paid time off.
- Employee assistance programs for mental health.
- Company-sponsored events and team-building activities.
- Diverse, professional, and inclusive work environment.
- Opportunities for career growth.
- Cutting-edge technology and tools.
- Family-friendly policies, including parental leave.
- Commuter benefits or transportation assistance.
- Social responsibility and community involvement programs.
04 positions
Full-time
On-site job
Work Schedule Timings:
Monday to Friday
Evening Shift (06 PM to 02 AM)
(transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
Clinical Trials Quality Assurance Associate (Night)
Posted 10 days ago
Job Viewed
Job Description
Minerva Research Solutions is a clinical trial management service provider.We aim to transform the landscape of healthcare and research with our quality clinical services. We support the biotech, medical, and pharma industries through all phases of the clinical trial lifecycle. Our services include Data Operation, Recruitment Services, and Regulatory. Our goal is to speed up the lifecycle of novel therapies through streamlined processes, stringent timelines & real-time solutions. Our clinical trial support services & consultations are tailored to foster your product and requirements.
We aim to deliver high-quality data and solutions to make your clinical trials a success. We follow stringent FDA and GCP regulations throughout all phases of the clinical trial process.
Minerva Research Solution is looking for dynamic individuals with a passion for ensuring the highest standards in clinical trial data quality assurance. As a key player in our team, you will play a crucial role in maintaining the integrity and accuracy of clinical trial data. Responsibilities: Perform comprehensive data-driven Quality Monitoring activities to ensure compliance with regulatory requirements and SOPs, and to ensure a continued state of inspection readiness. Ensure data is recorded under sponsor protocol, GCP guidelines, industry guidelines, and agency regulations. Perform quality control checks; identify and track source documentation errors and non-conformances with requirements. Provide ongoing compliance support including but not limited to: Preparing periodic clinical trial quality reports for assigned programs and assessing these reports with applicable clinical team members to identify areas of risk. Collaborates with applicable team members to develop risk mitigation plans. Collaborating with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and working with appropriate groups to implement Corrective Action Plans (CAPAs). Performs quality reviews of key documents developed for use in clinical trials and in preparation for submission to regulatory health authorities. Assist in preparing for all Sponsor and FDA audits. Assist in conducting internal audits to review key processes. Provide appropriate support to assigned cross-functional workgroups. Establishes effective partnerships with internal staff to facilitate the timely identification and resolution of compliance and quality matters and other opportunities for quality process improvement. Query resolution and data entry and questionnaire preparation regarding the respective studies. Other related Quality Assurance projects as assigned. The QA Associate will report to the Quality Assurance Lead Knowledge, Education, and Experience: Qualified Profession with strong medical background (Pharm-D, MBBS, BDS etc)with a keen interest in Clinical Research are strongly encouraged to apply. In-depth knowledge of FDA, GCP, ICH, and other state and federal agency guidelines for the conduct of clinical trials. Knowledge of IRB requirements. 1+ years in work related to Quality Control / Quality Assurance area in clinical research will preferred. Experience including external clinical/regulatory and document auditing will be a plus Skills and Abilities: Good communication skills (interpersonal, written, verbal) Strong attention to detail and good time management skills Flexible attitude concerning work assignments Ability to manage multiple and varied tasks in a fast-moving environment Ability to interact professionally at all levels within the organization. Knowledge of the HIPAA Privacy Act and its application to clinical research. Benefits:
Competitive salary and performance-based bonuses. Medical health insurance coverage. Employees Old-age benefits coverage. Flexible work hours and remote work options. Professional learning and developmentsupport. Generous vacation and paid time off. Employee assistance programs for mental health. Company-sponsored events and team-building activities. Diverse, professional, and inclusive work environment. Opportunities for career growth. Cutting-edge technology and tools. Family-friendly policies, including parental leave. Commuter benefits or transportation assistance. Social responsibility and community involvement programs. Openings:
04 positions Full-time On-site job
Work Schedule Timings: Monday to Friday Evening Shift (06 PM to 02 AM) (transport facility provided for female staff only and allowance for male employees, additional night shift allowance)
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Research Associate, Clinical Trials Unit Medical College
Posted 13 days ago
Job Viewed
Job Description
Medical College
Location IntroductionAga Khan University was established in 1983 as an international university with an objective to promote human welfare in general, and the welfare of the people in the countries in which it operates, by disseminating knowledge and providing instruction, training, research and service in the health sciences, education and such other branches of learning as the University may determine.
As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopt appropriate standards for safeguarding and promoting a respectful relationship with and between diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment.
Clinical Trials Unit (CTU) is a Department dedicated to develop a center of excellence for high quality and high impact clinical trials both nationally & internationally. The Department promotes AKU’s vision by providing leadership, consultation and facilitation in different phases of clinical trials in compliance with the International Standards and Good Clinical Practice (GCP) guidelines.
This is a grant-funded contractual position.
ResponsibilitiesYou will be responsible to:
- liaise and coordinate study requirements with relevant units and departments of the institution, in line with AKU institutional policies
- organize and/or administer the informed consent process in conjunction with the Principal Investigator
- coordinate and provide patient care in compliance with protocol requirements specific to patients screening, recruitment, scheduling, and study visit procedures
- disburse investigational product upon written authorization from the PI and provide relevant teaching with respect to its administration
- maintain study documentation as per protocol and GCP requirements (screening, subject recruitment, investigational drug accountability, enrolment, monitoring and study visit, adverse/serious adverse events etc.)
- review/monitor patients for changes such as in health status, response to investigational product, adverse events, compliance in use of investigational product, concomitant medication use, protocol compliance
- provide laboratory support services including phlebotomy and collection/handling of required specimens (e.g. stool, urine, nasal swabs) using standard techniques
- review clinical trials protocols and shared feedback with supervisors for approval
- facilitate internal and external audits of the unit
- draft and report SAE, annual/periodic reports to regulatory bodies and sponsor
You should have:
- a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field
- must have a current registration & be in good standing with their professional association
- at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other
- possess excellent clinical skills
- ability to work in independently and versatility to work in a variety of roles
- excellent written and verbal communication skills in English
- integrity and strong research ethics
- efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel).
- a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field
- must have a current registration & be in good standing with their professional association
- at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other
- possess excellent clinical skills
- ability to work in independently and versatility to work in a variety of roles
- excellent written and verbal communication skills in English
- integrity and strong research ethics
- efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel).
Interested candidates should send their detailed CVs to and mark the subject line with position number "10011569".
Only shortlisted candidates will be contacted.
Applications should be submitted latest by September 16, 2024
#J-18808-LjbffrResearch Associate, Clinical Trials Unit Medical College
Posted 10 days ago
Job Viewed
Job Description
Entity
Medical College Location
Introduction
Aga Khan University was established in 1983 as an international university with an objective to promote human welfare in general, and the welfare of the people in the countries in which it operates, by disseminating knowledge and providing instruction, training, research and service in the health sciences, education and such other branches of learning as the University may determine. As an equal opportunity employer, AKU believes in promoting a diverse and inclusive culture and is committed to adopt appropriate standards for safeguarding and promoting a respectful relationship with and between diverse workforce of its faculty, staff, trainees, volunteers, beneficiaries, wider communities, and other stakeholders with whom it works, including children and vulnerable adults and expects all employees/trainees and partners to share this commitment. Clinical Trials Unit (CTU) is a Department dedicated to develop a center of excellence for high quality and high impact clinical trials both nationally & internationally. The Department promotes AKU’s vision by providing leadership, consultation and facilitation in different phases of clinical trials in compliance with the International Standards and Good Clinical Practice (GCP) guidelines. This is a grant-funded contractual position. Responsibilities
You will be responsible to: liaise and coordinate study requirements with relevant units and departments of the institution, in line with AKU institutional policies organize and/or administer the informed consent process in conjunction with the Principal Investigator coordinate and provide patient care in compliance with protocol requirements specific to patients screening, recruitment, scheduling, and study visit procedures disburse investigational product upon written authorization from the PI and provide relevant teaching with respect to its administration maintain study documentation as per protocol and GCP requirements (screening, subject recruitment, investigational drug accountability, enrolment, monitoring and study visit, adverse/serious adverse events etc.) review/monitor patients for changes such as in health status, response to investigational product, adverse events, compliance in use of investigational product, concomitant medication use, protocol compliance provide laboratory support services including phlebotomy and collection/handling of required specimens (e.g. stool, urine, nasal swabs) using standard techniques review clinical trials protocols and shared feedback with supervisors for approval facilitate internal and external audits of the unit draft and report SAE, annual/periodic reports to regulatory bodies and sponsor Requirements
You should have: a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field must have a current registration & be in good standing with their professional association at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other possess excellent clinical skills ability to work in independently and versatility to work in a variety of roles excellent written and verbal communication skills in English integrity and strong research ethics efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel). a degree in Medicine, or Masters/Bachelors level in Nursing or in any relevant Health Field must have a current registration & be in good standing with their professional association at least one-year research experience with MBBS or 3 years clinical work experience in nursing or other possess excellent clinical skills ability to work in independently and versatility to work in a variety of roles excellent written and verbal communication skills in English integrity and strong research ethics efficiency in MS office tools (Microsoft Word, Microsoft PowerPoint and Microsoft Excel). Comprehensive employment reference checks will be conducted. To Apply
Interested candidates should send their detailed CVs to and mark the subject line with position number "10011569". Only shortlisted candidates will be contacted. Applications should be submitted latest by
September 16, 2024
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Project Management Executive
Posted 13 days ago
Job Viewed
Job Description
We're looking for a motivated Project Management Executive to support our project teams. This is a junior role ideal for candidates with a foundational understanding of project management and emerging technologies, looking to grow in a dynamic environment.
VentureDive Overview
Founded in 2012 by veteran technology entrepreneurs from MIT and Stanford, VentureDive is the fastest-growing technology company in the region that develops and invests in products and solutions that simplify and improve the lives of people worldwide. We aspire to create a technology organization and an entrepreneurial ecosystem in the region that is recognized as second to none in the world.
Key Responsibilities:
- Project Support: Assist in planning, executing, and monitoring project tasks. Help coordinate schedules, resources, and track progress.
- Communication : Facilitate internal team communication, Collaborate with cross-functional teams, draft project updates, and ensure all project documentation is organized and accessible.
- Documentation: Maintain project logs, reports, and assist with status updates.
Required Experience & Qualification:
- Education: Bachelor's degree in Computer Science, Engineering, or a related field.
- Communication: Strong communication skills (written and verbal). Proficiency in English is essential.
- PM Experience: General understanding of project management principles and At least some hands-on experience in project coordination or management, even in a supporting role (e.g., internships, part-time, or entry-level roles).
- Technical Acumen: Foundational knowledge in Software Engineering, Data Science, Data Engineering, and AI.
- Skills: Organized, detail-oriented, familiar with any PM tools (e.g. Jira, Asana, Trello). Proactive and a quick learner.
What we look for beyond required skills
In order to thrive at VentureDive, you
…are intellectually smart and curious
…have the passion for and take pride in your work
…deeply believe in VentureDive’s mission, vision, and values
…have a no-frills attitude
…are a collaborative team player
…are ethical and honest
Are you ready to put your ideas into products and solutions that will be used by millions?
You will find VentureDive to be a quick pace, high standards, fun and a rewarding place to work at. Not only will your work reach millions of users world-wide, you will also be rewarded with competitive salaries and benefits. If you think you have what it takes to be a VenDian, come join us . we're having a ball!
#LI-Onsite #J-18808-Ljbffr
Project Management Associate
Posted 13 days ago
Job Viewed
Job Description
At Creative Frontiers , we bringideas to life at the intersection of innovation, design, and technology. Wespecialize in high-quality Animation, E-learning solutions, UI/UX design,and full-scale digital development services . Our success lies in not just what wecreate but how we manage it — and that’s where you come in.
We’relooking for a skilled Project Management Associate to manage international client relationships,drive project delivery, and coordinate across cross-functional teams. A ProjectManager who thrives in dynamic environments and knowshow to keep projects running smoothly from start to finish. If you’re a masterof timelines, a natural communicator, and someone who can turn chaos into structure— we want to hear from you.
Key Responsibilities
- Client elationship Management: Act as the primary point of contact for clients post-acquisition, maintaining clear, consistent, and professional communication throughout the project lifecycle.
- Strategic Project Oversight: Lead project planning, execution, and delivery, ensuring alignment with client goals, timelines, and quality standards.
- Cross-Functional Coordination: Bridge communication between clients and internal teams (designers, animators, developers, learning specialists) to ensure cohesive progress.
- Timeline & Milestone Tracking: Monitor key project phases, manage deadlines, and deliver timely updates to all stakeholders.
- Feedback Implementation: Gather, analyze, and integrate client feedback effectively, ensuring deliverables align with expectations.
- Risk & Issue Management: Proactively identify risks or blockers and implement solutions to ensure project momentum and stability.
- Post-Project Evaluation: Conduct post-mortems and deliver insights for continuous improvement across project processes.
- Global Collaboration: Coordinate with teams based in Pakistan and maintain flexible availability to attend client meetings in EST and PST time zones when required.
Qualifications
- Bachelor’s degree in Computer Science, Digital Project Management, Operations Management Business Administration, Management, Economics, Social Sciences , or a related field.
- Relevant certifications such as CAPM, PMP, or Google Project Management Certificate are highly preferred.
Skills & Experience
- 1–3 years of project management or client-facing experience , preferably with international clients.
- Proficiency in project management tools such as Jira, Asana, Click Up , and the Microsoft Office Suite.
- Expertise in web development workflows , including UI/UX principles, CMS platforms (WordPress, Shopify, Webflow), and front-end/back-end concepts.
- Proficiency in design and development tools like Figma, Adobe Creative Suite, and prototyping software.
- Strong experience in Agile, Scrum, and Sprint planning , including running Scrum meetings and managing development cycles.
- Exceptional organizational skills with the ability to manage multiple projects and priorities simultaneously.
- Strong interpersonal and communication skills, with an aptitude for building trust and credibility across teams and clients.
- Experience in project documentation, status reporting, and scope management .
- Ability to conduct risk assessments , resolve conflicts, and apply negotiation skills in high-stakes scenarios.
- Familiarity with creative industry workflows (e.g., animation pipelines, instructional design, or UI/UX projects) is a significant advantage.
- Capable of balancing technical requirements and creative expectations to ensure successful outcomes.
Why Join Creative Frontiers?
- Diverse Creative Portfolio: Work on exciting and meaningful projects across animation, e-learning, digital design, and development.
- Growth & Learning: Access to continuous learning, training resources, and growth-oriented leadership.
- Inclusive Culture: A collaborative and respectful environment that values your input and expertise.
- Competitive Compensation: Market-aligned salary and flexible working hours to support work-life integration.
If you're ready to take on a role where project management truly drives creative and strategic outcomes , we’d love to hear from you.
To apply, send your CV to :
Subject Line : Project Management Associate – (Your Full Name)
Take the lead. Make an impact. Grow with us at Creative Frontiers.
Register your interest Thank you! Your submission has been received!Oops! Something went wrong while submitting the form.
#J-18808-LjbffrProject Management / QA
Posted 13 days ago
Job Viewed
Job Description
Reports To: Managing Director (Operationally)
Coordinates With: Chief Technology Officer (Technically)
Job Summary:
We are hiring a detail-driven QA, Jira & Bitbucket Coordinator to oversee software quality, task tracking in Jira, and repository coordination in Bitbucket. This hybrid role ensures all projects meet high-quality standards, team workflows are optimized, and reporting is streamlined. You'll report directly to the Managing Director and collaborate closely with the CTO.
Key Responsibilities:
- QA:
- Write and execute test cases for web, mobile, and backend projects.
- Conduct manual and automated testing.
- Log, track, and retest bugs; maintain test documentation.
- Jira:
- Administer task boards and workflows across departments.
- Assign and prioritize tasks based on sprint plans.
- Track team progress and generate weekly status reports.
- Bitbucket:
- Manage repository access and user permissions.
- Enforce branch, commit, and pull request workflows.
- Coordinate with developers for code management.
- Reporting:
- Provide structured progress and performance updates to the MD.
- Work with the CTO to maintain development standards.
- Collect weekly task plans from all employees and submit a consolidated plan to the MD every Monday.
- Prepare and submit end-of-week reports to the MD detailing task completion by each employee.
Key Performance Indicators (KPIs):
- Test case execution coverage and accuracy.
- Bug detection and resolution rate per sprint.
- Timeliness and accuracy of weekly reports.
- Jira workflow cleanliness and task completion rate.
- Bitbucket usage compliance and pull request hygiene.
Growth & Development Path:
This role offers a clear path toward QA Lead or Project Operations Manager based on performance, leadership, and contribution to process improvement. The ideal candidate will take increasing responsibility over time and may mentor junior QA or operational staff.
Requirements:
- Strong organizational, reporting, and follow-up skills.
- 2–4 years in a Product Management and/or QA role (preferably both).
- Strong understanding of SDLC, Agile/Scrum methodologies.
- Experience with QA tools (JIRA, Bitbucket, Postman, Selenium).
- Excellent communication, analytical, and problem-solving skills.
- A passion for building great products and ensuring quality.
Apply now and become a core part of a team that values both big-picture thinking and the fine details. Let’s build something great together.
Send your resume and portfolio at
Seniority levelEntry level
Employment typeFull-time
Job functionProject Management and Information Technology
IndustriesIT System Custom Software Development
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About the latest Healthcare project management Jobs in Pakistan !
Project Management Associate
Posted 13 days ago
Job Viewed
Job Description
Creative Frontiers , we bringideas to life at the intersection of innovation, design, and technology. Wespecialize in
high-quality Animation, E-learning solutions, UI/UX design,and full-scale digital development services . Our success lies in not just
what
wecreate but
how
we manage it — and that’s where you come in. We’relooking for a skilled
Project Management Associate
to manage international client relationships,drive project delivery, and coordinate across cross-functional teams. A ProjectManager who thrives in dynamic environments and knowshow to keep projects running smoothly from start to finish. If you’re a masterof timelines, a natural communicator, and someone who can turn chaos into structure— we want to hear from you. Key Responsibilities Client elationship Management:
Act as the primary point of contact for clients post-acquisition, maintaining clear, consistent, and professional communication throughout the project lifecycle. Strategic Project Oversight:
Lead project planning, execution, and delivery, ensuring alignment with client goals, timelines, and quality standards. Cross-Functional Coordination:
Bridge communication between clients and internal teams (designers, animators, developers, learning specialists) to ensure cohesive progress. Timeline & Milestone Tracking:
Monitor key project phases, manage deadlines, and deliver timely updates to all stakeholders. Feedback Implementation:
Gather, analyze, and integrate client feedback effectively, ensuring deliverables align with expectations. Risk & Issue Management:
Proactively identify risks or blockers and implement solutions to ensure project momentum and stability. Post-Project Evaluation:
Conduct post-mortems and deliver insights for continuous improvement across project processes. Global Collaboration:
Coordinate with teams based in Pakistan and maintain flexible availability to attend client meetings in EST and PST time zones when required. Qualifications Bachelor’s degree in
Computer Science, Digital Project Management, Operations Management Business Administration, Management, Economics, Social Sciences , or a related field. Relevant certifications such as
CAPM, PMP, or Google Project Management Certificate
are highly preferred. Skills & Experience 1–3 years of project management or client-facing experience , preferably with international clients. Proficiency in project management tools such as
Jira, Asana, Click Up , and the Microsoft Office Suite. Expertise in web development workflows , including UI/UX principles, CMS platforms (WordPress, Shopify, Webflow), and front-end/back-end concepts. Proficiency in design and development tools
like
Figma, Adobe Creative Suite, and prototyping software. Strong experience in Agile, Scrum, and Sprint planning , including running Scrum meetings and managing development cycles. Exceptional organizational skills with the ability to manage multiple projects and priorities simultaneously. Strong interpersonal and communication skills, with an aptitude for building trust and credibility across teams and clients. Experience in
project documentation, status reporting, and scope management . Ability to conduct
risk assessments , resolve conflicts, and apply negotiation skills in high-stakes scenarios. Familiarity with creative industry workflows (e.g., animation pipelines, instructional design, or UI/UX projects) is a significant advantage. Capable of balancing technical requirements and creative expectations to ensure successful outcomes. Why Join Creative Frontiers? Diverse Creative Portfolio:
Work on exciting and meaningful projects across animation, e-learning, digital design, and development. Growth & Learning:
Access to continuous learning, training resources, and growth-oriented leadership. Inclusive Culture:
A collaborative and respectful environment that values your input and expertise. Competitive Compensation:
Market-aligned salary and flexible working hours to support work-life integration. If you're ready to take on a role where
project management truly drives creative and strategic outcomes , we’d love to hear from you. To apply, send your CV to : Subject Line :
Project Management Associate – (Your Full Name) Take the lead. Make an impact. Grow with us at Creative Frontiers. Register your interest
Thank you! Your submission has been received!
Oops! Something went wrong while submitting the form.
#J-18808-Ljbffr
Project Management / QA
Posted 25 days ago
Job Viewed
Job Description
Managing Director (Operationally) Coordinates With:
Chief Technology Officer (Technically) Job Summary: We are hiring a detail-driven QA, Jira & Bitbucket Coordinator to oversee software quality, task tracking in Jira, and repository coordination in Bitbucket. This hybrid role ensures all projects meet high-quality standards, team workflows are optimized, and reporting is streamlined. You'll report directly to the Managing Director and collaborate closely with the CTO. Key Responsibilities: QA:
Write and execute test cases for web, mobile, and backend projects. Conduct manual and automated testing. Log, track, and retest bugs; maintain test documentation.
Jira:
Administer task boards and workflows across departments. Assign and prioritize tasks based on sprint plans. Track team progress and generate weekly status reports.
Bitbucket:
Manage repository access and user permissions. Enforce branch, commit, and pull request workflows. Coordinate with developers for code management.
Reporting:
Provide structured progress and performance updates to the MD. Work with the CTO to maintain development standards. Collect weekly task plans from all employees and submit a consolidated plan to the MD every Monday. Prepare and submit end-of-week reports to the MD detailing task completion by each employee.
Key Performance Indicators (KPIs): Test case execution coverage and accuracy. Bug detection and resolution rate per sprint. Timeliness and accuracy of weekly reports. Jira workflow cleanliness and task completion rate. Bitbucket usage compliance and pull request hygiene. Growth & Development Path: This role offers a clear path toward QA Lead or Project Operations Manager based on performance, leadership, and contribution to process improvement. The ideal candidate will take increasing responsibility over time and may mentor junior QA or operational staff. Requirements: Strong organizational, reporting, and follow-up skills. 2–4 years in a Product Management and/or QA role (preferably both). Strong understanding of SDLC, Agile/Scrum methodologies. Experience with QA tools (JIRA, Bitbucket, Postman, Selenium). Excellent communication, analytical, and problem-solving skills. A passion for building great products and ensuring quality. Apply now
and become a core part of a team that values both big-picture thinking and the fine details. Let’s build something great together. Send your resume and portfolio at
Seniority level
Entry level Employment type
Full-time Job function
Project Management and Information Technology Industries
IT System Custom Software Development
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Project Management Assistant
Posted today
Job Viewed
Job Description
About Us:
Reboot Monkey offers seamless data center management and colocation services, handling collocated infrastructure with expert care. Our remote hands support ensures smooth operations within data center facility around the clock. We pride ourselves on optimizing and managing data center environments efficiently, providing reliable and scalable solutions to meet the needs of our clients.
Key Responsibilities:
Project Planning and Coordination:
Develop detailed project plans, including timelines, budgets, and resource allocation for both client-facing and external data center projects.
Collaborate with the development team to define project scope, deliverables, and technical requirements for internal projects.
Cross-Team Collaboration:
Coordinate with the Project Manager to ensure smooth execution of internal projects, aligning on goals and timelines.
Work closely with cross-functional teams, including engineering, operations, and IT, to ensure alignment on project objectives.
Stakeholder Management:
Serve as the primary point of contact between clients, vendors, the development team, and external stakeholders.
Maintain clear communication with all stakeholders, managing expectations and providing regular project updates.
Risk Assessment and Mitigation:
Identify potential risks and challenges for client and internal projects.
Develop and implement risk mitigation strategies to ensure smooth execution.
Budget and Resource Management:
Monitor project budgets for internal and external initiatives, ensuring cost-effectiveness and adherence to financial constraints.
Allocate and manage resources, including personnel, equipment, and tools, to meet project requirements.
Regulatory Compliance:
Ensure all data center projects comply with local, national, and international regulations and standards.
Manage documentation and certifications required for project approvals and audits.
What We Offer:
Flexible working hours and fully remote work environment.
Opportunity to work with a talented and growing team on exciting projects in the tech space.
Access to professional development resources and ongoing learning opportunities.