72 Clinical jobs in Bahrain

• Conducting site selection, initiation, routine monitoring, and close-out visits to clinical research sites.
• Verifying that the rights and well-being of human subjects are protected, and that reported trial data are accurate, complete, and verifiable from source documents.
• Ensuring compliance with study protocols, GCP, regulatory requirements, and SOPs.
• Managing electronic case report forms (eCRFs) and query resolution processes.
• Providing ongoing training and support to site staff on study protocols and procedures.
• Reviewing regulatory documents, ensuring they are complete and maintained appropriately.
• Communicating effectively with investigators and site staff, fostering strong working relationships.
• Preparing monitoring reports and follow-up letters in a timely and accurate manner.
• Assisting in the preparation for regulatory inspections and internal audits.
• Identifying and escalating potential issues or risks to project management.

• Bachelor's degree in a life science, pharmacy, nursing, or related health field.
• Minimum of 2-3 years of experience as a Clinical Research Associate, preferably in a pharmaceutical company or CRO setting.
• Thorough understanding of ICH GCP guidelines and local regulatory requirements.
• Excellent communication, interpersonal, and presentation skills in English.
• Ability to work independently and as part of a collaborative team.
• Strong analytical and problem-solving abilities.
• Proficiency in Microsoft Office Suite and clinical trial management systems (CTMS).
• Willingness to travel frequently within Bahrain and occasionally regionally as required by study demands.
• Proven ability to manage multiple priorities and meet deadlines in a fast-paced environment.

• Conduct on-site, remote, and potentially central monitoring of clinical trials to ensure adherence to trial protocols, GCP, SOPs, and regulatory requirements.
• Verify source data against Case Report Forms (CRFs) and ensure accurate and complete documentation.
• Review Investigator Site Files (ISF) for completeness and accuracy.
• Train site staff on study protocols, data collection procedures, and regulatory requirements.
• Monitor patient recruitment and retention, providing strategies for improvement.
• Ensure the proper handling and accountability of investigational products.
• Identify and resolve discrepancies or issues at clinical sites, escalating complex problems to the Clinical Project Manager.
• Prepare monitoring visit reports and follow-up letters, documenting all findings and actions taken.
• Communicate effectively with site personnel, investigators, and internal study teams.
• Participate in site selection, initiation, and close-out visits.
• Ensure timely submission of regulatory documents and ethics committee approvals.
• Contribute to the overall quality and success of clinical trials by proactively addressing potential risks.
• Stay updated on relevant regulatory guidelines and industry best practices.

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related health scientific field.
• Minimum of 2-4 years of experience as a Clinical Research Associate or equivalent clinical trial monitoring experience.
• Strong understanding of Good Clinical Practice (GCP) and relevant regulatory guidelines (e.g., ICH, local regulations).
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Excellent written and verbal communication and interpersonal skills.
• Strong analytical and problem-solving abilities, with keen attention to detail.
• Ability to work independently, manage multiple priorities, and meet deadlines.
• Willingness to travel locally and potentially regionally for site visits as required.
• Ability to maintain strict confidentiality and ethical standards.
• Certification from a recognized clinical research organization is a plus.

• Conduct on-site and remote monitoring visits to clinical trial sites, ensuring adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Verify source data, ensure accurate and complete case report forms (CRFs), and resolve data discrepancies.
• Review investigator site files for accuracy and completeness.
• Provide training and support to site staff on study protocols, procedures, and regulatory compliance.
• Manage clinical trial supplies, ensuring proper inventory and documentation.
• Facilitate communication between clinical sites, sponsors, and internal teams.
• Identify, document, and report adverse events and protocol deviations in a timely manner.
• Assist in site selection and initiation processes.
• Participate in team meetings and contribute to the development of study-related documents.
• Prepare detailed monitoring visit reports and follow-up letters.
• Maintain up-to-date knowledge of clinical research regulations and industry trends.

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related health-scientific field.
• Minimum of 2-4 years of experience as a Clinical Research Associate, preferably with experience in multiple therapeutic areas.
• Strong understanding of ICH-GCP guidelines and relevant regulatory requirements.
• Excellent communication (written and verbal), interpersonal, and presentation skills.
• Exceptional organizational skills and attention to detail.
• Ability to travel frequently to clinical sites as required.
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Strong problem-solving abilities and a proactive approach to issue resolution.

• Conduct site qualification, initiation, monitoring, and close-out visits for assigned clinical trials, ensuring adherence to study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Verify source data, review case report forms (CRFs), and resolve data queries in a timely and efficient manner.
• Ensure the protection of study subjects by verifying informed consent processes, adverse event reporting, and adherence to ethical guidelines.
• Manage investigational product accountability, ensuring proper storage, dispensing, and return.
• Communicate effectively with investigators, site staff, and study sponsors, providing training and support as needed.
• Identify potential risks and issues at clinical sites, developing and implementing corrective action plans.
• Maintain accurate and comprehensive documentation of all site visits, communications, and activities.
• Assist in the preparation and submission of regulatory documents to ethics committees and health authorities.
• Provide ongoing support and mentorship to clinical site staff to ensure optimal study conduct.
• Participate in internal and external audits, ensuring audit readiness of assigned sites.
• Stay current with evolving clinical research regulations, guidelines, and industry best practices.
• Contribute to the development of study-specific documents, such as monitoring plans and site training materials.
• Facilitate effective communication channels between various study stakeholders.
• Manage trial master file (TMF) reconciliation and ensure its accuracy and completeness.
• Travel to clinical sites as required to perform monitoring activities.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related health field.
• Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) in a pharmaceutical company, CRO, or academic research setting.
• In-depth knowledge of ICH-GCP guidelines, regulatory requirements (e.g., FDA, EMA, local health authorities), and clinical trial processes.
• Proven experience in monitoring multiple clinical trials across different therapeutic areas.
• Strong understanding of medical terminology and clinical trial data.
• Excellent written and verbal communication skills, with strong attention to detail.
• Ability to work independently, prioritize tasks, and manage time effectively.
• Proficiency in electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Microsoft Office Suite.
• Strong problem-solving abilities and a proactive approach.
• Ability to travel frequently to clinical sites.
• Relevant professional certifications (e.g., CCRP) are a plus.
• Fluency in English is essential; Arabic is an advantage.

• Coordinate and manage all aspects of clinical trial operations, from study initiation to close-out, ensuring adherence to study protocols, Good Clinical Practice (GCP), and regulatory guidelines.
• Assist in the preparation and submission of regulatory documents to ethics committees and relevant authorities.
• Recruit and screen potential study participants, ensuring eligibility criteria are met and obtaining informed consent.
• Schedule and coordinate participant visits, tests, and procedures according to the study protocol.
• Collect, record, and maintain accurate and complete clinical data in case report forms (CRFs) and electronic data capture (EDC) systems.
• Ensure data quality, integrity, and timely submission, resolving any data queries in collaboration with data management teams.
• Monitor participant safety and well-being throughout the trial, reporting adverse events and serious adverse events promptly.
• Maintain comprehensive study files, including regulatory documents, source documents, and correspondence.
• Liaise effectively with investigators, study sponsors, CROs, and other research personnel.
• Prepare for and participate in internal and external audits and inspections.
• Manage study supplies, equipment, and biological samples, ensuring proper storage and handling.
• Educate participants and their families about the study procedures, potential risks, and benefits.
• Stay current with evolving clinical research regulations and best practices.
• Contribute to the development and revision of study-related documents and standard operating procedures (SOPs).

• Bachelor's degree in Nursing, Life Sciences, Pharmacy, Public Health, or a related healthcare field.
• A minimum of 2-4 years of experience as a Clinical Research Coordinator or in a similar role within a clinical trial setting.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements (e.g., ICH-GCP).
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent organizational skills, meticulous attention to detail, and ability to manage multiple priorities simultaneously.
• Strong communication (written and verbal) and interpersonal skills, with the ability to interact professionally with diverse stakeholders.
• Ability to work independently, exercise sound judgment, and resolve issues proactively.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
• Basic understanding of medical terminology and human anatomy/physiology.
• Demonstrated commitment to patient safety and data integrity.
• Certifications in clinical research (e.g., ACRP, SoCRA) are highly desirable.
• Ability to maintain strict confidentiality of patient information and study data.

• Conduct laboratory experiments and analyze data for drug development projects.
• Ensure strict adherence to Good Manufacturing Practices (GMP) and regulatory guidelines.
• Prepare detailed documentation for clinical trials and regulatory submissions.
• Collaborate with cross-functional teams including R&D, clinical, and quality assurance.
• Monitor and evaluate the safety and efficacy of pharmaceutical products.
• Stay updated on the latest scientific advancements and industry trends.

• Bachelor's degree in Pharmacy, Pharmaceutical Sciences, or Chemistry or a related discipline.
• 3-5 years of progressive experience in pharmaceutical R&D or quality control.
• Proven track record of experience with regulatory affairs and a strong understanding of drug lifecycle.
• Strong analytical rigor and precision abilities.
• Excellent communication skills, both written and verbal, in English. Arabic is a plus.

Our client, a leading pharmaceutical company dedicated to innovation and patient care, is seeking a highly meticulous and skilled Clinical Research Coordinator to join their dynamic research team in Hamad Town, Northern, BH . This is an exciting opportunity to contribute to groundbreaking clinical trials and make a significant impact on advancing medical science within a collaborative and highly regulated environment.

As a Clinical Research Coordinator , you will be responsible for managing and coordinating all aspects of clinical trials, ensuring adherence to protocols, regulatory guidelines, and ethical standards. We are looking for a professional who is passionate about clinical research, possesses strong organizational and interpersonal abilities, and thrives in a detail-oriented and fast-paced setting. This role demands a proactive individual with a keen eye for compliance, a commitment to patient safety, and the ability to manage complex study documentation with precision.

• Coordinate and manage clinical research studies from initiation to close-out, ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements.
• Assist in the screening, recruitment, and enrollment of study participants, ensuring informed consent is properly obtained.
• Collect, record, and maintain accurate and complete source documents, case report forms (CRFs), and other study-related data.
• Schedule and coordinate patient visits, diagnostic tests, and follow-up appointments.
• Administer study medications or interventions as per protocol and monitor patients for adverse events, reporting as required.
• Maintain effective communication with principal investigators, study sponsors, CROs, and other site staff.
• Prepare for and participate in internal and external audits, monitoring visits, and quality assurance reviews.
• Manage study supplies, equipment, and biological samples, ensuring proper storage and handling.

• Bachelor's degree in Nursing, Life Sciences, Pharmacy, or a related healthcare field.
• Minimum of 3-5 years of experience as a Clinical Research Coordinator or in a similar role within the pharmaceutical or clinical research industry.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements (e.g., FDA, ICH).
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent organizational skills and strong attention to detail in data collection and documentation.
• Exceptional interpersonal and communication skills, with the ability to interact empathetically with patients and professionally with colleagues.
• Ability to work independently and manage multiple research projects simultaneously.
• Current certification in GCP is highly desirable.

Our client fosters a culture of scientific inquiry, continuous learning, and patient-centric innovation. You will have the opportunity to work on diverse therapeutic areas and contribute to significant medical breakthroughs. We offer a competitive salary package, comprehensive benefits, and opportunities for career advancement within a leading pharmaceutical organization. If you are a dedicated and enthusiastic individual ready to take on new challenges and contribute to critical clinical research, we encourage you to apply and become a part of our success story. Join us in advancing healthcare from our state-of-the-art research facility in Hamad Town, Northern, BH . We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. Your expertise and dedication will be highly valued as we work together towards improving patient outcomes and contributing to medical progress.

• Conduct clinical trials in accordance with GCP guidelines (for CRA).
• Promote pharmaceutical products to healthcare professionals (for Sales Rep).
• Dispense medications accurately and provide patient counseling (for Pharmacist).
• Ensure compliance with pharmaceutical regulations and quality standards.
• Maintain detailed records and documentation for all activities.
• Collaborate with medical teams and research institutions.
• Stay updated on new drugs, therapies, and industry developments.
• Participate in training and continuous professional development programs.

• A Bachelor's degree in Pharmacy, Life Sciences, or a related medical field or a related discipline.
• 6+ years of progressive experience in pharmaceutical R&D, clinical operations, or medical sales.
• Demonstrated proficiency with clinical trial management systems, CRM for sales, or laboratory analysis software.
• Strong analytical, problem-solving, and decision-making skills.
• Excellent written and verbal communication skills in English; Arabic is a plus.
• Ability to work independently and as part of a collaborative team.
• Proven track record of meeting deadlines and managing multiple priorities.
• A keen eye for detail and a commitment to delivering high-quality results.

• Competitive salary and performance-based bonuses.
• Health insurance coverage.
• Opportunities for professional development and continuous learning.
• A vibrant and inclusive company culture.
• Work-life balance initiatives.
• Career progression pathways within a growing organization.

• Conduct pre-study, initiation, routine monitoring, and close-out visits at investigator sites according to study protocols and SOPs.
• Verify source data and ensure accuracy and completeness of Case Report Forms (CRFs), both paper and electronic.
• Ensure investigator sites are compliant with ICH-GCP guidelines, local regulatory requirements, and study protocols.
• Review regulatory documents at sites to ensure they are up-to-date and complete.
• Manage site performance, identifying and resolving issues related to patient recruitment, data quality, and compliance.
• Provide ongoing training and support to site staff on protocol requirements and data collection procedures.
• Communicate effectively with investigator site personnel, study coordinators, and internal study teams.
• Prepare comprehensive site visit reports and follow-up letters.
• Assist in the preparation and submission of regulatory documents to ethics committees and health authorities.
• Participate in internal and external audits as required.
• Identify and escalate potential safety issues or protocol deviations promptly.
• Manage trial supplies and drug accountability at sites.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare discipline.
• Minimum of 3-5 years of experience as a Clinical Research Associate, with independent monitoring experience.
• Strong knowledge of ICH-GCP guidelines, clinical trial processes, and regulatory requirements.
• Excellent organizational skills and attention to detail.
• Strong written and verbal communication skills.
• Proficiency in using Electronic Data Capture (EDC) systems and clinical trial management systems (CTMS).
• Ability to work independently and manage multiple sites concurrently.
• Strong problem-solving and analytical skills.
• Willingness and ability to travel frequently (up to 50-70% of the time).
• Valid driving license and access to a vehicle.
• Proficiency in Microsoft Office Suite.