87 Clinical Research jobs in Bahrain
Clinical Research Associate
70130 Amwaj Islands
BHD4500 Annually
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Our client, a leading pharmaceutical organization, is actively seeking a meticulous and driven Clinical Research Associate (CRA) to join their dedicated team in **Isa Town, Southern, BH**. This vital role is responsible for monitoring and managing clinical trials to ensure adherence to protocols, good clinical practice (GCP) guidelines, and all applicable regulatory requirements. The successful candidate will play a key role in the successful execution of clinical studies, contributing to the development of life-saving medications.
Responsibilities:
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.
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0
Clinical Research Associate
80610 Al Markh
BHD75000 Annually
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Our client is recruiting a dedicated and meticulous Clinical Research Associate (CRA) to support their clinical trial activities in Sanad, Capital, BH . This vital role ensures that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. The CRA will be responsible for monitoring clinical trial sites, verifying data accuracy and integrity, and ensuring patient safety. You will conduct site initiation visits, routine monitoring visits, and close-out visits, as well as essential document management. Key responsibilities include managing investigational product accountability, resolving data queries, and ensuring compliance with all regulatory requirements. Building and maintaining strong relationships with investigators and site staff is paramount. The ideal candidate will possess a Bachelor's degree in a life science or healthcare-related field, with at least 3 years of experience as a Clinical Research Associate. Thorough understanding of ICH-GCP, clinical trial processes, and regulatory requirements is essential. Strong organizational, communication, and problem-solving skills are required. The ability to travel to clinical trial sites is a prerequisite. This is an exciting opportunity to contribute to groundbreaking medical research and help bring new therapies to patients.
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1
Clinical Research Associate
1005 BH Bilad Al Qadeem, Capital
BHD65000 Annually
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Our client, a leading pharmaceutical innovator, is looking for an experienced Clinical Research Associate to join their expanding team in Manama, Capital, BH . This role is critical in supporting the execution of clinical trials, ensuring compliance with all relevant regulations and protocols, and contributing to the development of life-saving medications. The Clinical Research Associate will be responsible for site monitoring, data collection and verification, and maintaining accurate trial documentation. Key duties include identifying and qualifying study sites, training site staff, ensuring adherence to Good Clinical Practice (GCP) guidelines, and resolving data discrepancies. You will work closely with investigators, study coordinators, and internal project teams to facilitate the smooth running of trials and ensure patient safety and data integrity. This position requires a meticulous approach, strong organizational skills, and the ability to manage multiple tasks efficiently. The successful candidate will possess a Bachelor’s degree in a life science, nursing, or a related field, coupled with significant experience in clinical research. A thorough understanding of pharmaceutical industry standards, regulatory affairs, and clinical trial processes is essential. Excellent communication and problem-solving skills are a must. Travel to clinical sites will be required as needed. This is an exciting opportunity to be part of a forward-thinking company dedicated to advancing healthcare and to contribute to groundbreaking research in the heart of Manama.
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2
Clinical Research Associate
1022 Tubli, Central
BHD68000 Annually
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Our client is actively seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their growing pharmaceutical division in **Budaiya, Northern, BH**. This vital role involves supporting and managing clinical trials, ensuring adherence to protocols, and upholding the highest standards of data integrity and patient safety. The ideal candidate will be detail-oriented, possess strong organizational skills, and have a deep understanding of pharmaceutical research processes.
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.
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.
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3
Clinical Research Associate
1152 Hamad Town, Northern
BHD1500 month
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Posted 5 days ago
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Our client, a dynamic pharmaceutical company dedicated to advancing healthcare, is seeking a meticulous and driven Clinical Research Associate to join their team in **Hamad Town, Northern, BH**. This vital role supports the execution of clinical trials, ensuring adherence to protocols, regulations, and ethical standards. The ideal candidate will possess a strong scientific background and experience in clinical trial management. Key responsibilities include:
- Monitoring clinical trial sites to ensure compliance with protocols, Good Clinical Practice (GCP) guidelines, and applicable regulations.
- Verifying the accuracy, completeness, and consistency of clinical data collected at study sites.
- Ensuring proper documentation, including source documents, case report forms (CRFs), and investigational product accountability.
- Communicating effectively with investigators, site staff, and study sponsors to resolve discrepancies and address issues.
- Conducting site initiation visits, interim monitoring visits, and close-out visits.
- Training site personnel on study procedures, protocols, and data collection requirements.
- Ensuring patient safety and reporting adverse events and serious adverse events promptly.
- Managing study supplies and ensuring proper storage and handling of investigational products.
- Reviewing and reconciling study data, identifying and resolving data queries.
- Participating in the development and finalization of clinical trial documentation, such as protocols and informed consent forms.
- Ensuring compliance with all relevant pharmaceutical industry regulations and ethical guidelines.
- Maintaining organized and up-to-date study files and essential documents.
- Collaborating with internal teams, including data management, regulatory affairs, and project management.
- Reporting on site progress, challenges, and key findings to study management.
- Upholding the highest standards of data integrity and scientific rigor.
- A Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field. A Master's degree is a plus.
- Minimum of 2-3 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial monitoring role.
- In-depth knowledge of GCP guidelines, ICH regulations, and clinical trial processes.
- Strong understanding of medical terminology and clinical trial methodologies.
- Excellent attention to detail and accuracy in data review and documentation.
- Proficiency in clinical data management software and electronic data capture (EDC) systems.
- Effective communication, interpersonal, and organizational skills.
- Ability to travel to study sites as required.
- Proficiency in both written and spoken English.
- A proactive approach to problem-solving and the ability to work independently.
- Familiarity with the pharmaceutical and healthcare landscape in **Hamad Town, Northern, BH** is beneficial.
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4
Clinical Research Associate
205 Durrat Al Bahrain
BHD70000 Annually
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Posted 5 days ago
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Our client, a leading pharmaceutical innovator, is searching for a meticulous and dedicated Clinical Research Associate (CRA) to join their team in Jidhafs, Capital, BH . This role is pivotal in ensuring the successful execution of clinical trials, adhering strictly to Good Clinical Practice (GCP) guidelines and regulatory requirements. The CRA will be responsible for monitoring study sites, verifying the accuracy and completeness of data, ensuring patient safety, and managing the overall conduct of trials. Key responsibilities include site initiation visits, routine monitoring visits (on-site and remote), data review and query resolution, and close-out visits. You will serve as the primary liaison between the sponsor and the investigative sites, fostering strong working relationships with principal investigators and study staff.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, coupled with demonstrable experience as a CRA or in a similar clinical research role. A thorough understanding of ICH-GCP guidelines, clinical trial protocols, and regulatory affairs is essential. Strong organizational skills, excellent attention to detail, and the ability to manage multiple tasks and priorities effectively are critical. The candidate must possess outstanding interpersonal and communication skills, with the ability to build rapport and influence stakeholders at all levels. Proficiency in clinical trial management software and electronic data capture (EDC) systems is a significant advantage. This position involves frequent travel to clinical trial sites, requiring flexibility and a valid driver's license. Our client offers a competitive compensation package, comprehensive benefits, and ample opportunities for professional growth and development within the pharmaceutical industry. If you are passionate about advancing medical treatments and ensuring the highest standards in clinical research, this is the role for you. Join us in making a difference in patient lives through rigorous scientific investigation.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field, coupled with demonstrable experience as a CRA or in a similar clinical research role. A thorough understanding of ICH-GCP guidelines, clinical trial protocols, and regulatory affairs is essential. Strong organizational skills, excellent attention to detail, and the ability to manage multiple tasks and priorities effectively are critical. The candidate must possess outstanding interpersonal and communication skills, with the ability to build rapport and influence stakeholders at all levels. Proficiency in clinical trial management software and electronic data capture (EDC) systems is a significant advantage. This position involves frequent travel to clinical trial sites, requiring flexibility and a valid driver's license. Our client offers a competitive compensation package, comprehensive benefits, and ample opportunities for professional growth and development within the pharmaceutical industry. If you are passionate about advancing medical treatments and ensuring the highest standards in clinical research, this is the role for you. Join us in making a difference in patient lives through rigorous scientific investigation.
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5
Clinical Research Associate
3005 Amwaj Islands
BHD70000 Annually
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Posted 5 days ago
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A leading pharmaceutical company with a strong commitment to innovation and patient well-being is looking for a dedicated Clinical Research Associate to join their esteemed team in Isa Town, Southern, BH . This role is pivotal in ensuring the successful execution of clinical trials, adhering strictly to regulatory guidelines and ethical standards. The ideal candidate will have a background in life sciences or a related field, coupled with substantial experience in clinical trial management. Your responsibilities will encompass site initiation, monitoring, and close-out visits, ensuring data integrity and patient safety throughout the trial lifecycle. You will be the primary point of contact for investigative sites, providing training and support to site personnel, and resolving any issues that may arise. A critical aspect of this role involves meticulous document management, including trial master file maintenance and regulatory submission preparation. The successful applicant will possess a deep understanding of ICH-GCP guidelines and local regulatory requirements. Excellent organizational skills, attention to detail, and strong analytical abilities are essential for success. You must be adept at communicating effectively with cross-functional teams, including investigators, study coordinators, and internal stakeholders. This position offers a dynamic work environment with the opportunity to contribute to groundbreaking medical advancements. We are seeking individuals who are proactive, possess strong problem-solving skills, and are passionate about improving healthcare outcomes. A bachelor's degree in a relevant scientific discipline is required; a master's degree or higher is preferred. Previous experience as a CRA or in a similar clinical research role is mandatory. If you are driven by scientific discovery and wish to make a tangible impact in the pharmaceutical industry, we encourage you to apply. This role involves regular travel to clinical sites.
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6
Clinical Research Associate
BH13 Seef, Capital
BHD85000 Annually
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Posted 5 days ago
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Job Description
Our client, a pioneering pharmaceutical company in **Janabiyah, Northern, BH**, is actively searching for a meticulous and dedicated Clinical Research Associate (CRA) to join their expanding clinical operations team. This vital role will be instrumental in the successful execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. The CRA will be responsible for monitoring study sites, data collection, and maintaining comprehensive documentation.
Primary Responsibilities:
Qualifications:
This is an outstanding opportunity to make a significant impact on advancing healthcare by participating in cutting-edge research in the growing pharmaceutical sector of **Janabiyah, Northern, BH**.
Primary Responsibilities:
- Conducting site initiation visits, interim monitoring visits, and site closure visits according to protocol and regulatory guidelines.
- Ensuring compliance with Good Clinical Practice (GCP) and applicable regulatory requirements.
- Verifying the accuracy, completeness, and integrity of clinical data collected at study sites.
- Training and supporting study site personnel on trial protocols and procedures.
- Managing communication between study sites, the sponsor, and regulatory authorities.
- Maintaining detailed study documentation and regulatory files.
- Identifying and reporting adverse events and protocol deviations.
- Resolving data queries and ensuring timely data entry.
- Assisting in the preparation of study-related documents, including protocols and case report forms (CRFs).
- Contributing to the overall quality and success of clinical research projects.
Qualifications:
- Bachelor's degree in a life science, nursing, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Experience with various therapeutic areas is a plus.
- Proficiency in clinical trial management systems (CTMS) and Electronic Data Capture (EDC) systems.
- Excellent attention to detail and organizational skills.
- Strong written and verbal communication skills.
- Ability to travel to study sites as required.
- Problem-solving skills and the ability to work independently.
This is an outstanding opportunity to make a significant impact on advancing healthcare by participating in cutting-edge research in the growing pharmaceutical sector of **Janabiyah, Northern, BH**.
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7
Clinical Research Coordinator
101 Riffa, Southern
BHD60000 Annually
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Our client, a respected community healthcare provider in Riffa, Southern, BH , is seeking a dedicated and detail-oriented Clinical Research Coordinator to join their dynamic team. This role is crucial in facilitating the smooth execution of clinical trials, ensuring patient safety, data integrity, and adherence to regulatory guidelines. The successful candidate will work closely with physicians, patients, and research sponsors to manage all aspects of clinical research studies.
Responsibilities:
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.
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8
Clinical Research Scientist
10256 Busaiteen, Muharraq
BHD75000 Annually
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Posted 1 day ago
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Our client, a leading pharmaceutical research and development company situated in Busaiteen, Muharraq, BH , is seeking a highly skilled and dedicated Clinical Research Scientist. This role is critical to advancing our pipeline of innovative therapeutics through meticulous planning, execution, and analysis of clinical trials. The ideal candidate will possess a strong scientific background, extensive experience in clinical research methodologies, and a commitment to upholding the highest standards of data integrity and regulatory compliance. You will contribute to groundbreaking studies that have the potential to transform patient care.
Responsibilities:
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.
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