74 Clinical Research Associate jobs in Pakistan

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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As decided by the executive heads, Granule Services wants to onboard more employees for the post of Medical Research Writer .

We require candidates applying for this post to hold at least a BS degree in a medical technology field that includes Pathology, Respiratory Therapy, Surgical Technology, or Ophthalmology. MBBS or BS in Nursing is also acceptable. We encourage fresh graduates to apply; our company is focused on providing a bright career path for you, and it is a full-time office-based writing job.

As a part of Granule Services, you will receive a market competitive salary. You will also be entitled to fuel allowance, semi-annual bonuses, annual increments, provident funds, annual leaves, and paid training.

Job Specification

The ideal candidate should have a strong understanding of medical terminology. Fresh graduates are encouraged to apply. This is a full-time office-based job.

Our office is located in the vicinity of DHA Phase 6, Karachi.

Marketing and Advertising - Karachi, Pakistan

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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 :

• 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

Instructor (Research), Department of Medicine Entity

Medical College

Location Introduction

Aga Khan University, chartered in 1983 as Pakistan's first private international university, is committed to the provision of education, research and health care of international standard relevant to Pakistan and the region. The affiliated Aga Khan University Hospital has well-equipped investigative services and provides state-of-the-art clinical facilities.

The Department of Medicine comprises of independent sections of Cardiology, Dermatology, Endocrinology, Gastroenterology, Internal Medicine, Infectious Diseases, Nephrology, Neurology, and Pulmonary & Critical Care. The department has over 70+ full-time Faculty with a strong commitment to undergraduate and postgraduate education and research. Residency Programmes are offered in Internal Medicine, Neurology, Adult Cardiology, Gastroenterology, Pulmonary Medicine, Nephrology and Dermatology, as well as Fellowship Programmes in Clinical Neurophysiology & Electrodiagnostic Medicine, Diabetes, Endocrinology & Metabolism, Interventional Cardiology and Infectious Diseases.

This is a grant-funded contractual position.

Responsibilities

The incumbent must clear the IBA Karachi entry exam, interview and secure admission in MSDS programme at IBA Karachi. Specifically, you will be responsible to:

• develop and execute NCD (cardiovascular diseases and Stroke) related surveillance or implementation research project focusing on cardiovascular disease, stroke or their risk factors. The project will be supported by AKUPI NCD Fogarty grant, once approved by leadership committee
• publish two manuscripts as a first author in their two-year tenure
• disseminate research and knowledge to wider audiences
• participate in university, national and international research conferences and symposiums.
• participate with team in project brainstorming and operationalization other than ones own project. 

Requirements

You should have:

• a Bachelor's degree in Computers Sciences or at least a minimum of 16 years of education in Science subjects with commitment to practice Data Science in the NCD health domain. Non-Computer science (CS) candidates can only be inducted in the fall semester and CS/IT candidates can only be inducted in the Spring semester. Therefore, potential candidates should strictly comply with this requirement when they appear for the admission test
• experience of working at an academic institution /university as a research faculty will be an added advantage. Long term commitment to NCD research, and interest in NCD is also a added advantage 
• excellent interpersonal communication skills and commitment to learning, growth, and self-development
• ability to work in teams
• integrity and strong research ethics
• ability to provide conceptual and technical input to a diverse range of research studies in the department and the institution
• track record of demonstrated scholarship through research and publication
• obtained research grants or publications
• good teaching skills and knowledge of new teaching methodologies and practices
• good academic writing skills
• proficiency in the use of related computer software packages
• ability to build and promote partnerships across the organization and beyond.

To Apply

Interested candidates should send their detailed CVs by email to and mark the position number ‘10052003’ in the subject line. 

Only shortlisted candidates will be contacted.

Applications should be submitted latest by September 1, 2024

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Instructor (Research), Human Development Programme Entity

Medical College

Location Introduction

The Human Development Programme (HDP) aims to support human development through a multidisciplinary and research-based approach. Its initial focus is early childhood, a period of life that lays the foundation for all future learning, development and wellbeing. Applying an integrated approach to education, health, nutrition and stimulation in early years. HDP aims to provide the support needed to promote holistic child development by enhancing physical, cognitive, social and emotional abilities of children to help them become healthy competent individuals participating productively and effectively in their societies.

HDP is determined to promote better development of future generations and with its educational and community-based programmes. The Programme aims to build the capacity of professionals, parents and communities who have the responsibility of providing a strong foundation and learning opportunities for ensuring a good start in life to every child.

This is a grant-funded contractual position.

Responsibilities

You will be responsible to:

• ensure implementation of all project activities
• manage day to day operations of the project
• monitor project goals and objectives
• develop training manual, power point presentations and other training materials
• develop schedules according to project timelines
• oversee all training logistic arrangement
• organize and facilitate quarterly and annual review meetings with partners
• write quarterly and annual project reports
• attend regular meetings with stakeholders.

Requirements

You should have:

• a Master's degree in a discipline related to ECD
• at least five years experience in designing and conducting projects in education or early child development
• good experience of conducting/coordinating trainings and capacity building
• excellent supervisory, interpersonal, team building and communication skills
• sound knowledge of qualitative research methods
• strong communication skills in English, Urdu and other local languages
• willingness for extensive travel all over Pakistan.

To Apply

Interested candidates should send their detailed CVs by email to and mark the subject with position number “10051819”.

Only shortlisted candidates will be contacted.

Applications should be submitted latest by July 28, 2024

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