83 Clinical Data jobs in Bahrain
Clinical Trials Project Manager
00974 Tubli, Central
BHD95000 Annually
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Posted 1 day ago
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Our client is looking for a dedicated and skilled Clinical Trials Project Manager to oversee clinical research operations in Nuwaidrat, Southern, BH . This role is crucial in ensuring the successful planning, execution, and completion of clinical trials in accordance with regulatory standards and project timelines. The Project Manager will be responsible for managing all aspects of clinical trials, from site selection and initiation to patient recruitment, data collection, and study closeout. Key responsibilities include:
- 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.
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0
Clinical Research Associate - Pharmaceutical Trials
78901 Bilad Al Qadeem, Capital
BHD9000 Annually
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Posted 4 days ago
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Our client, a leading pharmaceutical research organization, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in **Manama, Capital, BH**. This critical role will involve overseeing and managing clinical trials, ensuring adherence to protocols, good clinical practices (GCP), and regulatory requirements. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits, as well as ensuring data quality and patient safety. You will act as the primary liaison between the sponsor and the clinical sites, building strong relationships with investigators and study staff. Key responsibilities include verifying the accuracy and completeness of study data, monitoring patient eligibility, and ensuring all study-related procedures are conducted according to the approved protocol. The ideal candidate will have a strong understanding of clinical trial processes, regulatory guidelines, and medical terminology. Excellent organizational, communication, and problem-solving skills are essential. This position requires the ability to travel to clinical trial sites, often internationally. We are looking for a proactive individual with a keen eye for detail and a commitment to ethical research practices. Your contribution will be vital in advancing pharmaceutical development and bringing new treatments to patients. This is a challenging and rewarding career opportunity for professionals passionate about clinical research and patient well-being. Success in this role demands meticulous attention to detail and a deep understanding of the complex regulatory landscape of pharmaceutical trials.
Responsibilities:
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.
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1
Clinical Research Associate - Pharmaceutical Trials
551 Northern, Northern
BHD60000 Annually
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Posted 4 days ago
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Our client, a leading pharmaceutical company with operations in Shakhura, Northern, BH , is looking for a diligent and detail-oriented Clinical Research Associate (CRA) to support the execution of clinical trials. The CRA will be responsible for monitoring clinical trial sites, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. Key responsibilities include site initiation visits, interim monitoring visits, and close-out visits, verifying the accuracy and completeness of source documentation and case report forms (CRFs), and managing study-related documentation. You will also be involved in training site personnel on study procedures, resolving data queries, and ensuring timely data collection. The ideal candidate will have a Bachelor's degree in a life science, health science, or a related field. A minimum of 3 years of experience as a CRA or in a similar clinical research role within the pharmaceutical industry is required. Strong knowledge of ICH-GCP guidelines and regulatory requirements is essential. Excellent organizational skills, meticulous attention to detail, and strong written and verbal communication skills are necessary. The ability to travel to clinical trial sites as needed and manage multiple projects simultaneously is also required. This role offers the opportunity to contribute to the development of life-saving medicines and gain valuable experience in global clinical research.
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2
Senior Clinical Research Associate - Oncology Trials
245E Zinj, Capital
BHD7200 month
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Our client, a leading biopharmaceutical company, is seeking a highly experienced Senior Clinical Research Associate (CRA) to manage and oversee oncology clinical trials. This vital role ensures that trials are conducted, recorded, and reported in accordance with protocol, standard operating procedures (SOPs), and regulatory requirements (e.g., ICH-GCP). The Senior CRA will be responsible for site selection, initiation, monitoring, and close-out visits to ensure data integrity and patient safety. Key responsibilities include identifying, evaluating, and recommending potential clinical trial sites; initiating sites according to protocol and regulatory guidelines; monitoring study conduct through on-site and remote visits; ensuring accurate and timely data collection and query resolution; managing site-level documentation; ensuring investigator compliance with protocol and regulatory standards; providing training and support to investigators and site staff; and preparing and submitting regulatory documents. A Bachelor's degree in a life science, nursing, or related field is required; an advanced degree or nursing qualification is a plus. A minimum of 5 years of experience as a CRA, with a significant portion focused on oncology clinical trials, is essential. Strong knowledge of ICH-GCP guidelines and regulatory requirements is mandatory. Excellent monitoring skills, meticulous attention to detail, and outstanding communication and interpersonal abilities are critical for success. This impactful role is located in the medical research vicinity of Tubli, Capital, BH .
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3
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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4
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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5
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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6
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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7
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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8
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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