805 Pharmaceutical Project jobs in Pakistan

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 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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Research Associate, Clinical Trials Unit

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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Key Responsibilities:

• Assist in developing and maintaining comprehensive project plans, schedules, documentation, and reports.

• Coordinate tasks between internal teams and external stakeholders to ensure timely execution of project deliverables.

• Monitor project progress, track key milestones, and proactively identify and escalate potential risks or delays.

• Organize and participate in meetings, prepare meeting minutes, and follow up on assigned action items.

• Support in defining and managing project scope, objectives, and change requests, ensuring alignment with business goals.

• Maintain accurate and up-to-date records across project management tools such as Jira, Trello, or Asana.

• Foster collaboration among teams by facilitating effective communication and ensuring clarity in task responsibilities.

• Assist in preparing progress updates and performance reports for internal reviews and client updates.

• Ensure all project activities are aligned with organizational processes, quality standards, and compliance guidelines.

• Contribute to continuous improvement initiatives by identifying bottlenecks and suggesting process enhancements.

Qualifications:

• Bachelor’s degree in Computer Science, Software Engineering, or Computer Engineering is preferred.

• Candidates with BBA or BSc degrees will also be considered if they demonstrate a strong interest in project management.

• 0–2 years of relevant experience in project coordination or a related role.

• Must have a genuine interest in project management — this role is for individuals who are serious about building a career in this field.

• Familiarity with project management tools (e.g., Jira, Trello, Asana ) is a plus.

• Strong organizational, communication, and time management skills.

• Ability to multitask , handle shifting priorities, and meet deadlines in a collaborative team environment.

• A proactive, detail-oriented mindset with a willingness to learn and grow professionally.

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Description and Summary

At PwC, our talent and development professionals focus on identifying, deploying, training, and enabling talent through employee skill enhancement and fostering a culture of continuous learning and professional growth. They collaborate with subject matter experts and project teams to strategize effective ways to locate, assess, educate, and train employees, aligned with market developments and firm strategy.

Those in cross-border mobility at PwC implement and administer policies for international assignments, facilitate accurate allowance payments, ensure tax compliance, and coordinate administrative tasks related to expatriates to meet government regulations.

Building meaningful client relationships, managing and inspiring others, navigating complex situations, and growing personal and technical expertise are key aspects of this role. Anticipating team and client needs, delivering quality work, and embracing ambiguity are expected. Asking questions and viewing uncertainty as growth opportunities are encouraged.

Skills, Knowledge, and Experiences

• Respond effectively to diverse perspectives, needs, and feelings.
• Utilize tools, methodologies, and techniques to generate ideas and solve problems.
• Apply critical thinking to analyze complex concepts.
• Understand project objectives and their alignment with overall strategy.
• Develop a broader understanding of the changing business context.
• Use reflection to develop self-awareness, enhance strengths, and address development areas.
• Interpret data to inform insights and recommendations.
• Uphold professional and technical standards, including PwC guidance, code of conduct, and independence requirements.

Key Responsibilities

• Project Leadership: Lead planning, execution, and monitoring of transformation projects aligned with strategic objectives.
• Performance Monitoring: Track progress, analyze metrics, and prepare status reports for stakeholders and senior management.
• Change Management: Develop and implement strategies for smooth transitions and stakeholder engagement.
• Best Practices Implementation: Promote and apply best practices in project management and transformation initiatives.
• Relationship Management: Build and maintain positive relationships with clients, partners, and stakeholders.

Required Skills and Qualifications

• Excellent data management and analytics skills.
• Proficiency in Microsoft Excel and PowerPoint.
• Bachelor's or Master's degree in Business Administration, Management, or related fields.
• ACCA affiliates are encouraged to apply.

Required Experience

• 2 to 3 years of relevant project management experience.

Please note that this is not a technical position.

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Location: Gulberg Greens, Islamabad.

We are seeking a dynamic and detail-oriented Project Coordinator to join our team. The successful candidate will play a vital role in managing and coordinating projects across diverse domains, ensuring timely completion, quality standards, and seamless communication between stakeholders.

Key Responsibilities:

Coordinate project activities and ensure all team members are aligned on objectives and deadlines.

Develop and maintain project schedules, timelines, and budgets.

Act as a liaison between clients, internal teams, and vendors to ensure project requirements are met.

Monitor project progress and prepare regular status reports.

Identify and mitigate risks and issues that may impact project delivery.

Ensure compliance with industry standards and company policies.

Support the procurement process by tracking and managing materials and resources.

Organize and facilitate project meetings, including documenting minutes and follow-ups.

Job Specification

Good organizational and multitasking skills.

Good communication and interpersonal abilities.

Basic Know how of project management tools (e.g., MS Project, or equivalent).

Ability to work under pressure and meet deadlines.

Knowledge of technical aspects related to HVAC, MEP, ELV, or iBMS is an advantage.

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Job Description

Sumato Solutions is a reliable software company that offers digital solutions to businesses globally. Our key services are custom software solutions, digital automation, staff augmentation, and digital marketing. We provide scalable solutions that empower businesses and encourage talent to develop and grow in a collaborative workspace.As part of our growth, we are looking for a Project coordinator who is organized and proactive in managing projects within the field of software. It is an excellent opportunity in the practical field of dealing with software project management, working with various teams, and meeting deadlines.

Key Responsibilities

• Plan the various projects and coordinate the activities, timelines, and allocation of resources to allow the smooth and effective running of a project.
• Organize all project activities per day, communication with team members, and assist in monitoring progression to comply with deadlines.
• Coordinate day-to-day project activities, follow ups and assist in monitoring the progress of projects to deliver on time.
• Create updates, presentations, and summaries to support communication with the clients, professionally and in time.
• Keep project documentation, reports, and post-job meeting notes in order and line.
• Establish a communication channel in each department to understand project requirements and deliverables.
• Gain and practice project coordination best practices, tools, and frameworks to become a full-time project coordinator.
• Check project progress, deadlines, and report delays, risks, or hiccups for timely resolution.
• Make use of the project management software such as Jira, ClickUp, Trello, or Asana to log tasks, dependencies, and team activities.
• Take part in quality control measures to make sure that ongoing projects are in compliance with internal standards and expectations of its clients.
• Manage project coordination best practices such as scrum methodology, tools, and frameworks, to become a full-time project coordinator.

Requirements

• Bachelor's degree in CS, IT, SE, or any relevant degree.
• 1 to 2 years of experience in supporting and project management, especially in the software sector.
• Understanding of project management methodologies, task coordination, and project workflows.
• Strong communication and interpersonal skills to effectively collaborate with multiple teams.
• Good organizational and time management skills, with the ability to prioritize tasks.
• Skills in using MS Office and Google Workspace (Docs, Sheets, Slides, and so on).
• Ability to work in a fast-paced, deadline-driven environment.
• Proficient in coordinating project tasks and timelines using tools such as Jira, Trello, Asana, etc.

Company Benefits

• Market Competitive Salary
• Weekend Off
• Paid Annual Leaves
• Personal Growth
• Work Anniversaries & Birthdays Celebrations
• Performance-Based Increment

Working Hours

Monday - Friday; 9:00 am to 6:00 pm

Take The Lead In A Role Where Structure Meets Strategy!

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Join to apply for the PROJECT COORDINATOR role at GE Solucions

Support project head, client, and team by strategizing, problem-solving, and proposing operational improvements. Manage social media, marketing, website content, and international e-commerce. Analyze project impact, gather feedback, and drive ongoing enhancements. Prepare detailed progress reports and streamline workflows for projects.

Job Requirements

1. 1+ years of experience, working as a Project Manager, Coordinator, or similar Project Lead roles.
2. Excellent Communication and negotiation skills.
3. Possesses exceptional task management abilities ensuring timely completion without missing deadlines.
4. Experience working with Marketing and Technical teams with the ability to juggle multiple projects simultaneously.
5. A bachelor’s degree or equivalent with a major in Marketing is preferred.
6. Knowledge about Shopify, Magento, and other eCommerce Marketplaces will be a plus.

Job Offerings

• Salary Package: Rs.45,000 – Rs.70,000
• Growth & Learning Exposure
• Health Insurance
• Performance Bonus based on client’s satisfaction
• Annual Appraisal
• Cordial Work Environment

Job Details

• Working Days: Monday – Saturday
• Shift Timings: 02:00 pm – 11:00 pm (Saturday alternate)
• Location: PECHS, Block 6, Karachi

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Other

Industries

• Information Services

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About Us:
The Pakistan Press Foundation (PPF) is a non-profit organization committed to promoting press freedom and enhancing the standards of journalism in Pakistan. Founded in 1968, PPF advocates for the safety of journalists, supports investigative journalism, and has been instrumental in pioneering legislative changes to protect media professionals. Our work spans across advocacy, training, and global engagement to uphold freedom of expression and foster a vibrant media landscape.

Role Summary:
PPF is looking for a motivated Project Coordinator to join our dynamic team. This individual will be responsible for coordinating and implementing a range of projects aimed at advancing press freedom, journalist safety, and media development. The ideal candidate will have experience in project management within the NGO sector, excellent communication skills, and a strong commitment to PPF's mission.

Key Responsibilities:
- Coordinate the planning, implementation, and managing of long-term projects.
- Facilitate the development of project plans, goals, and deliverables in collaboration with project stakeholders.
- Monitor project progress, adjusting schedules and resources as needed to meet project objectives.
- Prepare and maintain project documentation, including reports, proposals, and presentations for stakeholders.
- Organize and participate in stakeholder meetings, and ensure effective communication and collaboration among project teams.
- Manage project budgets and ensure financial accountability and reporting.
- Evaluate project outcomes and impact, providing insights for future project improvements.

Job Specification

• Four-year Bachelor's degree in Project Management, Business Administration, Social Sciences, or related field. A Master's degree is preferred.
• At least 3 years of experience in project coordination or management, preferably within an NGO.
• Strong understanding of project management principles and tools.
• Excellent organizational, time management, and multitasking skills.
• Proficient in project management software.
• Exceptional communication and interpersonal skills, with the ability to work effectively in a team environment.

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