9 Clinical Data Manager jobs in Pakistan

Product Assistant (WordPress, Mixpanel, Google Analytics, Jira, Communication, Data Analysis, Research, Agile/Scrum methodology) Product Assistant (WordPress, Mixpanel, Google Analytics, Jira, Communication, Data Analysis, Research, Agile/Scrum methodology)

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Human Resources Recruiting Specialist at WMPU DEV and Incsub

As part of Incsub, since 2006, WPMU DEV, with its’ award-winning WordPress plugins, hosting, world-beating support, and site management tools, has helped millions of web developers, freelancers, and agencies run and grow their businesses.

We’re looking for a Product Assistant, who will play a key role in supporting the product team by researching user needs, gathering feedback, and helping prioritize product improvements that align with business goals.

You’ll collaborate closely with cross-functional teams—including designers, developers, QA, and writers—to plan and deliver sprint cycles aimed at enhancing product performance and user experience. Your responsibilities will include identifying user pain points, assisting in defining solutions, and continuously iterating based on feedback. Beyond product development, you’ll also contribute to fostering a positive and engaged team environment, helping ensure smooth communication and productive collaboration across all stages of the product lifecycle.

Responsibilities

* Organize and maintain the project backlog and roadmap

* Gather user feedback and conduct market research to help prioritize product features

* Assist in sprint planning, coordination, and retrospectives

* Collaborate with developers, designers, QA, and copywriters to address bugs and develop solutions

* Support user testing and data analysis using tools like MixPanel and Google Analytics

* Facilitate team communication, daily updates, and regular meetings

* Ensure timely responses to support queries and monitor feature requests

* Communicate product updates and changes to internal teams

* Contribute to documentation, blog posts, FAQs, and other product-related content

* Help define project requirements and success metrics with leadership

* Promote team engagement through activities and feedback loops

Qualifications

Essential attributes and experience required:

* Strong organizational and time management skills with the ability to multitask and prioritize effectively

* Excellent written and verbal communication skills, including the ability to create clear documentation and briefs

* Proactive problem-solving mindset with a keen attention to detail and a flexible, adaptable attitude

* Experience collaborating with cross-functional teams, including design, development, marketing, and support

* Familiarity with Agile and Scrum methodologies and participation in sprint planning and retrospectives

* Comfortable using project management tools like Jira to track tasks and progress

* Research and data analysis skills, including the ability to gather, interpret, and act on user feedback

* Hands-on experience with analytics tools such as Google Analytics, and MixPanel

* Experience in managing WordPress plugins development team; preferably experience with performance plugins, such as caching, image optimization, speed optimization, CDN integration, and performance testing

* Basic understanding of UX/UI principles and a curiosity for improving user experience

* Confident in facilitating meetings, stand-ups, and team check-ins to keep workflows aligned and on track

WordPress, Mixpanel, Google Analytics, Jira, English language, Communication, Data Analysis, Research, Agile/Scrum methodology

Why Join us?

* Growth-oriented culture.

* Excellent compensation with competitive benefits and rejuvenation time-off.

* Flexible work environment.

* Training, tools, and support will be provided to help you perform your job.

* Limitless learning opportunities by working with cutting-edge tech stacks and a diverse, talented team.

* 28 days of paid leave per annum (up to 35 days).

* Opportunities for paid travel to attend WordCamps and other industry conferences.

* Long service leaves (3 months off paid) after you’ve been with us for 10 years.

* Annual bonus based on company growth targets

* Technology budget that can help you upgrade the tools you use for your job; the longer you serve, the higher the budget.

* General expenses budget yearly that can be used to help you become more productive; the longer you work, the more you get.

What should i do now?

Download the Product Assistant Task, answer those questions, and then submit your application. It’s that simple!

The ability to write in clear English is essential in this role. We are unable to consider applications that fail to demonstrate a high level of written communication.

HIRING PROCESS

Our hiring process includes the task mentioned above and an interview with our management team. If a candidate successfully passes the interview stage, they will be offered a paid trial of 4-6 weeks before being offered a more permanent role.

Good luck!

Seniority level

• Seniority level Entry level

Employment type

• Employment type Full-time

Job function

• Job function Product Management and Marketing
• Industries Technology, Information and Internet

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QA Associate Night Shift (Clinical Trials)

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 Solutions 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 in accordance with 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. Collaborate with applicable team members to develop risk mitigation plans.
• Collaborate with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and work with appropriate groups to implement Corrective Action Plans (CAPAs).
• Perform 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.
• Establish 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:

• Medical Graduate 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.
• 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 with respect to 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 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.
• Professional learning and development support.
• 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: Full-time

Work Schedule Timings: Monday to Friday, 6 PM to 2 AM (transport facility provided for female staff only and allowance for male employees).

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QA Associate Night Shift (Clinical Trials)

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 Solutions 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 in accordance with 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. Collaborate with applicable team members to develop risk mitigation plans. Collaborate with the Clinical Team to share audit/inspection observations for lessons learned across protocol, and/or program, and work with appropriate groups to implement Corrective Action Plans (CAPAs). Perform 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. Establish 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: Medical Graduate 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. 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 with respect to 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 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. Professional learning and development support. 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:

Full-time Work Schedule Timings:

Monday to Friday, 6 PM to 2 AM (transport facility provided for female staff only and allowance for male employees).

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Job Description :

Key Responsibilities :

• Organize, maintain, and update company databases
• Ensure accuracy, consistency, and security of data
• Develop and implement data management strategies
• Collaborate with cross-functional teams to support data needs
• Generate reports and insights to support business decisions
• Utilize tools such as Microsoft Word, Excel, and PowerPoint for documentation, analysis, and presentation

Job Specification :

• Minimum 2 years of hands-on experience in data management or a related field.
• Proficient in data tools and database systems.
• Strong attention to detail and analytical skills.
• Bachelor's degree in Computer Science, IT, Business, or a related field.

Job Rewards and Benefits : Medical #J-18808-Ljbffr

Job Description :

Key Responsibilities : Organize, maintain, and update company databases Ensure accuracy, consistency, and security of data Develop and implement data management strategies Collaborate with cross-functional teams to support data needs Generate reports and insights to support business decisions Utilize tools such as Microsoft Word, Excel, and PowerPoint for documentation, analysis, and presentation Job Specification :

Minimum 2 years of hands-on experience in data management or a related field. Proficient in data tools and database systems. Strong attention to detail and analytical skills. Bachelor's degree in Computer Science, IT, Business, or a related field. Job Rewards and Benefits : Medical #J-18808-Ljbffr

Data Management Specialist - Remote
AutoScale Ventures, Pakistan

VinAudit.com Inc. is seeking a talented Data Management Specialist who will play an important role in executing important business data analysis and overseeing data production for quantitative and qualitative reports!

You would join a small team of 25 individuals working remotely and globally including in the Philippines, Pakistan, the United States, and Canada.

We specialize in vehicle data. Since 2011, we have aggregated billions of vehicle-related records, helped millions of consumers evaluate a car purchase, and served thousands of automotive businesses with access to our unique datasets.

We believe we're just getting started, and we'd love to explore how you could help.

Core Hours & Benefits:

• Location: Pakistan
• Core Hours: Monday - Friday, 9am - 5pm Seattle Time
• Base Pay : $3 USD/hr
• Benefits: HealthCare Coverage, Leave Days & Vacation Time, Paid Holidays, Equipment Funds

Job Specification

This role involves:

• Manage assigned tasks ensuring data meet the standard quality report
• Review pertinent data and build detailed reports for upper management
• Formulate techniques for quality data collection to ensure adequacy, accuracy and legitimacy of data
• Analyze and interpret large amounts of data
• Coordinate the production of data by the assigned department and by other data developers
• Field data-related questions and assist with client-support requests
• Organize documentation for recurring business processes
• Conduct in-depth web research on various topics
• Support and collaborate with various development tasks

Required experience:

• Strong organizational skills
• High-level verbal and written communication collaboration skills
• Detail-oriented with an eye for perfection
• Savvy with computers and familiar with modern, high-tech databases and IT systems
• Excellent understanding of data administration and management functions (collection, analysis, distribution etc.)
• Proficient at digesting, understanding, and analyzing large amounts of data and ability to translate complex problems clearly
• Review prepared data to ensure it is adequate, accurate, and complies with the standard requirements
• Consistently and independently productive with minimum supervision
• Passionate about self-development and continuous improvement

Resource Requirement:

• Stable internet connection (with a potential backup connection available)
• Available 100% exclusively (no other commitments)

Note: We aim to give our candidates the best experience possible. This means we will only get in touch if you have been shortlisted for the role. Thank you!

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Job Description :

• Maintain accurate records of financial transactions
• Data entry and verification of daily business operations
• Reconcile and maintain accounts
• Prepare and analyze reports as needed
• Support the finance team in daily administrative tasks

Job Specification :

• Strong knowledge of accounting principles
• Proficient in MS Office and accounting software
• Excellent attention to detail and organizational skills
• Ability to handle data with confidentiality

Job Rewards and Benefits : Medical #J-18808-Ljbffr

Job Description :

Maintain accurate records of financial transactions Data entry and verification of daily business operations Reconcile and maintain accounts Prepare and analyze reports as needed Support the finance team in daily administrative tasks Job Specification :

Strong knowledge of accounting principles Proficient in MS Office and accounting software Excellent attention to detail and organizational skills Ability to handle data with confidentiality Job Rewards and Benefits : Medical #J-18808-Ljbffr