83 Clinical Data jobs in Bahrain
Clinical Trials Project Manager
Posted 1 day ago
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- Developing comprehensive clinical trial protocols and study plans.
- Identifying, evaluating, and selecting clinical trial sites and investigators.
- Overseeing patient recruitment and retention strategies.
- Managing trial budgets and ensuring adherence to financial plans.
- Monitoring trial progress, data quality, and regulatory compliance.
- Liaising with regulatory authorities and ethics committees.
- Managing and mentoring clinical research associates (CRAs) and other study personnel.
- Ensuring the timely submission of clinical study reports and regulatory documents.
- Proactively identifying and mitigating risks associated with clinical trial execution.
- Maintaining effective communication with all stakeholders, including internal teams, investigators, and sponsors.
- Bachelor's or Master's degree in a life science, healthcare, or related field.
- Minimum of 7 years of experience in clinical research, with at least 3 years in a project management capacity.
- In-depth knowledge of Good Clinical Practice (GCP), ICH guidelines, and other relevant regulatory requirements.
- Proven experience in managing multiple clinical trials simultaneously.
- Strong leadership, organizational, and negotiation skills.
- Excellent interpersonal and communication skills, with the ability to build strong relationships with diverse stakeholders.
- Proficiency in clinical trial management software and data analysis tools.
- Demonstrated ability to manage complex projects under pressure and meet strict deadlines.
Clinical Research Associate - Pharmaceutical Trials
Posted 4 days ago
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Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits.
- Ensure compliance with study protocols, GCP, and regulatory requirements.
- Verify the accuracy and completeness of clinical trial data.
- Monitor patient safety and report adverse events.
- Act as a liaison between study sponsors and clinical trial sites.
- Build and maintain strong relationships with investigators and site staff.
- Ensure proper documentation and record-keeping at study sites.
- Train site personnel on study-specific procedures.
- Review and reconcile study-related documents.
- Contribute to the development of study protocols and clinical study reports.
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial role.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements.
- Experience in therapeutic areas relevant to pharmaceutical research.
- Excellent monitoring and site management skills.
- Strong data management and attention to detail.
- Proficiency in clinical trial management systems (CTMS) and EDC systems.
- Excellent communication, interpersonal, and presentation skills.
- Ability to travel frequently to clinical trial sites.
- Strong organizational and problem-solving abilities.
Clinical Research Associate - Pharmaceutical Trials
Posted 4 days ago
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Senior Clinical Research Associate - Oncology Trials
Posted today
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Clinical Research Associate
Posted today
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Job Description
Responsibilities:
- Conduct site visits (initiation, interim, and close-out) to assess protocol compliance, data accuracy, and overall study progress.
- Verify that all clinical trial activities are conducted in accordance with the study protocol, GCP, and regulatory requirements.
- Ensure accurate, complete, and timely entry of data into clinical trial databases.
- Monitor source documents and compare them against case report forms (CRFs) for discrepancies.
- Manage communication between study sites and the sponsor, addressing any issues or queries promptly.
- Train study site personnel on protocol requirements, study procedures, and data collection.
- Oversee the investigational product accountability and ensure proper storage and handling.
- Prepare site visit reports and follow up on action items with study sites.
- Ensure all essential documents are maintained in the Investigator Site File (ISF) and Trial Master File (TMF).
- Identify and report adverse events (AEs) and serious adverse events (SAEs) according to protocol.
- Contribute to the development of study protocols, CRFs, and other study-related documents.
- Participate in investigator meetings and training sessions.
- Ensure timely submission of all required regulatory documents.
- Maintain strong working relationships with investigators, site staff, and internal project teams.
- Actively participate in the resolution of site-level issues and deviations.
- Report on site performance and identify potential risks or challenges.
- Bachelor's degree in a life science, nursing, pharmacy, or a related scientific field. Advanced degree is a plus.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- Thorough understanding of GCP guidelines, ICH regulations, and clinical trial processes.
- Experience with various therapeutic areas is preferred.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication abilities, with attention to detail.
- Ability to travel frequently to clinical trial sites (estimated 50-70% travel).
- Proficiency in English; knowledge of Arabic is an advantage.
- Ability to work independently and as part of a cross-functional team.
- Strong analytical skills and the ability to interpret complex data.
Clinical Research Associate
Posted today
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Clinical Research Associate
Posted today
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Clinical Research Coordinator
Posted today
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Responsibilities:
- Recruit, screen, and enroll eligible participants into clinical trials according to protocol requirements.
- Obtain informed consent from participants, ensuring they fully understand the study procedures, risks, and benefits.
- Schedule participant visits, including medical evaluations, laboratory tests, and study-specific procedures.
- Collect, manage, and maintain accurate and complete study data, ensuring compliance with Good Clinical Practice (GCP) guidelines.
- Administer study medications or placebos as per protocol, maintaining meticulous records of administration and inventory.
- Monitor participants for adverse events and report any findings promptly to the principal investigator and regulatory bodies.
- Prepare and maintain all necessary study documentation, including case report forms (CRFs), source documents, and investigational product accountability logs.
- Assist with regulatory submissions and correspondence with Institutional Review Boards (IRBs) and ethics committees.
- Coordinate with external laboratories, pharmacies, and vendors involved in the research study.
- Communicate effectively with the research team, physicians, and study sponsors to ensure seamless trial operations.
- Stay updated on the latest developments in clinical research and relevant therapeutic areas.
- Bachelor's degree in Nursing, Biology, Health Sciences, or a related field.
- Minimum of 3 years of experience as a Clinical Research Coordinator or in a similar research role.
- In-depth knowledge of clinical trial phases, study designs, and regulatory requirements (e.g., ICH-GCP, FDA regulations).
- Experience with electronic data capture (EDC) systems and electronic health records (EHR).
- Excellent organizational, time management, and multitasking abilities.
- Strong communication and interpersonal skills, with the ability to interact empathetically with patients and their families.
- Proficiency in medical terminology and understanding of disease processes relevant to clinical trials.
- Ability to work independently and as part of a collaborative team.
- Attention to detail and a commitment to maintaining data accuracy and integrity.
- Certification from a recognized clinical research professional body (e.g., SoCRA, ACRP) is highly desirable.
Clinical Research Scientist
Posted 1 day ago
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Job Description
Responsibilities:
- Design and develop clinical trial protocols, ensuring scientific validity and alignment with regulatory requirements.
- Oversee the operational aspects of clinical trials, including site selection, initiation, monitoring, and close-out.
- Collaborate with cross-functional teams, including medical affairs, regulatory affairs, data management, and biostatistics.
- Analyze clinical trial data, interpret results, and prepare comprehensive study reports.
- Contribute to the writing of regulatory submission documents (e.g., INDs, NDAs) and scientific publications.
- Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other relevant guidelines.
- Manage external collaborations with clinical sites, investigators, and contract research organizations (CROs).
- Develop and present scientific findings at internal meetings and external conferences.
- Stay current with scientific literature, emerging technologies, and therapeutic area advancements.
- Contribute to the strategy and planning of future clinical development programs.
- Ensure the safety and well-being of study participants throughout the trial lifecycle.
- Ph.D. or equivalent doctoral degree in a relevant life science, biomedical science, or related field.
- Minimum of 5 years of experience in clinical research, with a focus on clinical trial design and execution within the pharmaceutical industry.
- Strong understanding of drug development processes, clinical trial phases, and regulatory pathways.
- Proven experience in data analysis, interpretation, and scientific writing.
- Excellent knowledge of GCP, ICH guidelines, and regulatory submission requirements.
- Demonstrated ability to manage complex projects and cross-functional teams.
- Strong analytical, problem-solving, and critical thinking skills.
- Effective communication and presentation skills, with the ability to convey complex scientific information clearly.
- Experience in therapeutic areas such as oncology, immunology, or cardiovascular diseases is highly desirable.
- Ability to work independently and as part of a collaborative team in a fast-paced environment.
Clinical Research Associate
Posted 1 day ago
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Job Description
Primary responsibilities include site selection, initiation, monitoring, and closing of clinical trial sites. You will be responsible for ensuring that clinical trials are conducted, recorded, and reported in accordance with the trial protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and other applicable regulatory requirements. This involves performing source data verification, reviewing study documentation, and ensuring accurate and timely data entry into clinical databases. The CRA will also liaise with investigators and site staff, address protocol deviations, and manage investigational product. Additionally, you will be responsible for preparing for and participating in regulatory inspections and audits.
Qualifications required include a Bachelor's degree in a life science, nursing, or a related field. A Master's degree is an advantage. Prior experience as a CRA or in a similar role within the pharmaceutical or biotechnology industry is essential, preferably with experience in Phase II or III trials. A thorough understanding of ICH-GCP guidelines and regulatory requirements is mandatory. Excellent communication, interpersonal, and problem-solving skills are necessary. The ability to travel to clinical sites (approximately 50-60%) is required. Strong computer skills, including proficiency with clinical trial management systems and electronic data capture (EDC) systems, are important. This is an exceptional opportunity to contribute to the development of life-saving medications and advance your career in clinical research.