What Jobs are available for Senior Cra in Bahrain?
Showing 553 Senior Cra jobs in Bahrain
Clinical Research Associate (CRA)
23006 Al Muharraq, Muharraq
BHD85000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking an experienced and meticulous Clinical Research Associate (CRA) to join their dedicated team. This position, based in **Jidhafs, Capital, BH**, plays a vital role in ensuring the successful execution and integrity of clinical trials. You will be responsible for monitoring study sites, ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. This role requires a highly organized individual with excellent attention to detail and strong communication skills.
Key responsibilities include site initiation, routine monitoring visits, and study close-out procedures. You will verify the accuracy and completeness of source data and ensure proper investigational product accountability. The CRA will also be responsible for resolving data queries, training site staff, and building strong working relationships with investigators and their teams. Effective communication with the study team, including project managers and data management personnel, is crucial. You will also be tasked with preparing monitoring reports and ensuring that all trial-related documentation is maintained in an organized and timely manner.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field. A minimum of 3 years of direct experience as a CRA, with a proven track record of managing multiple clinical trial sites independently, is required. Comprehensive knowledge of ICH-GCP guidelines and regulatory requirements is essential. Strong understanding of clinical trial processes from start to finish. Excellent organizational and time management skills, with the ability to prioritize tasks effectively. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is necessary. This is an excellent opportunity for a motivated CRA to contribute to the development of innovative therapies and advance their career within a dynamic pharmaceutical environment.
Key responsibilities include site initiation, routine monitoring visits, and study close-out procedures. You will verify the accuracy and completeness of source data and ensure proper investigational product accountability. The CRA will also be responsible for resolving data queries, training site staff, and building strong working relationships with investigators and their teams. Effective communication with the study team, including project managers and data management personnel, is crucial. You will also be tasked with preparing monitoring reports and ensuring that all trial-related documentation is maintained in an organized and timely manner.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field. A minimum of 3 years of direct experience as a CRA, with a proven track record of managing multiple clinical trial sites independently, is required. Comprehensive knowledge of ICH-GCP guidelines and regulatory requirements is essential. Strong understanding of clinical trial processes from start to finish. Excellent organizational and time management skills, with the ability to prioritize tasks effectively. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is necessary. This is an excellent opportunity for a motivated CRA to contribute to the development of innovative therapies and advance their career within a dynamic pharmaceutical environment.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Associate (CRA)
1300 Manama, Capital
BHD70000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their pharmaceutical research team in Manama, Capital, BH . This hybrid role involves monitoring clinical trials to ensure they are conducted, recorded, and reported in accordance with protocol, standard operating procedures, and good clinical practices (GCP). You will be responsible for site selection, initiation, monitoring, and closure activities, ensuring data accuracy and patient safety. The ideal candidate possesses a strong understanding of clinical trial regulations, protocol adherence, and ethical considerations in research. You will conduct site visits, review source documents, verify data integrity, and provide training and support to study site personnel. This position requires excellent organizational skills, attention to detail, and the ability to communicate effectively with investigators, study coordinators, and internal stakeholders. Travel to clinical trial sites will be a component of this role. We are looking for a proactive individual who can manage multiple studies and sites effectively, ensuring timely and accurate data collection. Your role is critical in the successful execution of clinical trials and the development of new pharmaceutical products. You will be responsible for identifying and resolving site-level issues, escalating concerns as needed, and ensuring compliance with all regulatory requirements. A strong understanding of medical terminology and study protocols is essential.
Responsibilities:
Responsibilities:
- Conduct site initiation, interim, and close-out visits.
- Monitor clinical trial sites to ensure compliance with protocol, GCP, and regulatory requirements.
- Verify accuracy and completeness of clinical trial data by reviewing source documents.
- Ensure patient safety and data integrity throughout the trial.
- Train and support site staff on study procedures and regulatory requirements.
- Prepare and submit monitoring reports in a timely manner.
- Identify and resolve site-specific issues and deviations.
- Maintain effective communication with investigators, study coordinators, and internal teams.
- Ensure all necessary documentation is maintained at the study sites.
- Participate in study team meetings and contribute to trial progress.
- Bachelor's degree in a life science, nursing, pharmacy, or a related field.
- 2+ years of experience as a Clinical Research Associate.
- In-depth knowledge of GCP guidelines and regulatory requirements.
- Experience with clinical trial monitoring and data verification.
- Strong understanding of medical terminology and clinical trial processes.
- Excellent organizational and time management skills.
- Proficiency in MS Office Suite and clinical trial management systems (CTMS).
- Strong written and verbal communication skills.
- Ability to travel to clinical trial sites as required.
- Detail-oriented with strong problem-solving abilities.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Associate (CRA)
241 BH Al Muharraq, Muharraq
BHD80000 Annually
WhatJobs
Posted 3 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical research organization, is seeking a highly competent Clinical Research Associate (CRA) to join their team. This hybrid role offers a dynamic mix of remote work and essential site visits, allowing for effective management of clinical trials. You will play a critical role in ensuring the quality and integrity of clinical trial data by monitoring study sites, verifying protocol adherence, and ensuring compliance with regulatory requirements. The ideal candidate will have a strong understanding of clinical trial processes, excellent attention to detail, and exceptional organizational skills. This position requires a proactive approach to problem-solving and the ability to build strong relationships with investigators and site staff.
Responsibilities:
Qualifications:
This is an excellent opportunity for a motivated CRA to contribute to significant pharmaceutical research in **Jidhafs, Capital, BH**, benefiting from a flexible hybrid work arrangement that balances remote responsibilities with crucial on-site activities.
Responsibilities:
- Monitor clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and applicable regulations.
- Verify the accuracy, completeness, and timeliness of study data through source document verification.
- Conduct pre-study, initiation, monitoring, and close-out visits at clinical trial sites.
- Identify and report any deviations from the protocol, regulatory requirements, or GCP.
- Train and educate site staff on study procedures, data collection, and regulatory requirements.
- Resolve data discrepancies and ensure resolution of site issues in a timely manner.
- Maintain clear and concise communication with study sites, project teams, and management.
- Prepare monitoring visit reports and ensure timely submission.
- Manage study supplies and ensure proper storage and handling of investigational products.
- Contribute to the development and review of study-related documents.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with various therapeutic areas is a plus.
- Excellent verbal and written communication skills.
- Strong organizational and time management abilities.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Ability to travel to clinical sites as required.
- Demonstrated problem-solving and critical-thinking skills.
This is an excellent opportunity for a motivated CRA to contribute to significant pharmaceutical research in **Jidhafs, Capital, BH**, benefiting from a flexible hybrid work arrangement that balances remote responsibilities with crucial on-site activities.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate (CRA)
320 Tubli
BHD75000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company dedicated to improving global health, is seeking a highly motivated and detail-oriented Clinical Research Associate (CRA) to join their team in **Isa Town, Southern, BH**. This critical role involves ensuring the quality and integrity of clinical trials conducted in accordance with Good Clinical Practice (GCP) guidelines and regulatory requirements. As a CRA, you will be responsible for site selection, initiation, monitoring, and close-out activities for clinical research studies. You will conduct site visits to verify protocol compliance, review source documents, manage data collection, and ensure the safety of study participants. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory affairs, and medical terminology. Excellent communication, organizational, and interpersonal skills are essential for effective collaboration with investigators, site staff, and internal study teams. A Bachelor's degree in a life science, nursing, or a related field is required, along with significant experience as a CRA. This position offers the opportunity to work on cutting-edge research in **Isa Town, Southern, BH**, contributing to the development of life-saving therapies. You will be instrumental in advancing medical science and ensuring that new treatments meet the highest standards of safety and efficacy. Our client values professional development and offers a supportive work environment with opportunities for career advancement within the pharmaceutical industry. This role requires frequent travel to clinical trial sites within the designated region.
Responsibilities:
Responsibilities:
- Perform site selection, initiation, monitoring, and close-out visits.
- Ensure compliance with study protocols, SOPs, and regulatory requirements (e.g., GCP, FDA).
- Verify the accuracy, completeness, and consistency of clinical data.
- Review essential documents and source data for accuracy and completeness.
- Manage and resolve site-level issues and discrepancies.
- Provide training and support to site staff on study procedures.
- Monitor patient safety and report adverse events promptly.
- Build and maintain strong relationships with investigators and site personnel.
- Prepare visit reports and contribute to study documentation.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate.
- Thorough understanding of GCP, ICH guidelines, and regulatory requirements.
- Excellent knowledge of clinical trial processes and documentation.
- Strong analytical and problem-solving skills.
- Exceptional communication, interpersonal, and organizational skills.
- Ability to travel frequently to clinical trial sites (approximately 60-70% travel).
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Attention to detail and commitment to data accuracy and integrity.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate (CRA)
00021 Riffa, Southern
BHD80000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a highly organized and diligent Clinical Research Associate (CRA) to support their ongoing clinical trials. This hybrid role involves monitoring clinical trial sites, ensuring adherence to protocols, and maintaining data integrity. You will play a key role in the successful execution of studies, contributing to the development of life-changing therapies. While offering flexibility, this position requires regular on-site presence at clinical sites and collaboration with the local team in **Riffa, Southern, BH**.
Key Responsibilities:
Key Responsibilities:
- Conduct site initiation, monitoring, and close-out visits in accordance with clinical trial protocols and Good Clinical Practice (GCP) guidelines.
- Ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, company standards, and regulatory requirements.
- Verify the accuracy, completeness, and validity of clinical trial data by reviewing source documents and case report forms (CRFs).
- Train and support investigators and site staff on trial procedures, regulatory requirements, and data management.
- Monitor site compliance with investigational product accountability and storage requirements.
- Identify and report adverse events and protocol deviations to the study team and regulatory authorities as required.
- Build and maintain strong working relationships with investigators, site staff, and internal study team members.
- Prepare visit reports and ensure timely follow-up on action items.
- Contribute to the development of study-related documents, such as protocols and case report forms.
- Stay current with industry trends and regulatory guidelines related to clinical research.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, 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 GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Proven experience in conducting site visits and monitoring clinical data.
- Excellent understanding of medical terminology and disease states relevant to the company's therapeutic areas.
- Strong organizational, time management, and problem-solving skills.
- Exceptional written and verbal communication skills.
- Ability to work independently and manage multiple priorities effectively.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate (CRA)
1010 Manama, Capital
BHD70000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical research organization, is seeking a meticulous and dedicated Clinical Research Associate (CRA) to join our growing team. This role offers a hybrid work arrangement, balancing remote responsibilities with essential site visits and office-based collaboration in Manama, Capital, BH . You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. This includes site initiation, routine monitoring, and close-out visits, as well as data verification, source document review, and issue resolution. You will serve as the primary liaison between the study sites and the sponsor, fostering strong working relationships and ensuring efficient trial conduct. A deep understanding of clinical trial processes, regulatory affairs, and medical terminology is essential. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is required. The ideal candidate will possess a Bachelor's degree in a life science or healthcare-related field, with proven experience as a CRA or in a related clinical research role. Excellent organizational, problem-solving, and communication skills are critical for success. We are looking for a detail-oriented professional with a commitment to ethical research and patient safety. This is an exciting opportunity to contribute to groundbreaking pharmaceutical research and advance your career in clinical development.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate (CRA)
611 Tubli
BHD70000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and meticulous Clinical Research Associate (CRA) to support their ongoing clinical trials. This role is fully remote, allowing you to contribute to groundbreaking research from anywhere. You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, regulations, and Good Clinical Practice (GCP) guidelines. Key responsibilities include site initiation, routine monitoring visits, site close-out, and ensuring the accuracy and integrity of clinical data. You will act as a liaison between the sponsor and the investigative sites, providing training and support to study coordinators and investigators. Identifying and resolving site-level issues, including protocol deviations and data discrepancies, is crucial. You will review essential documents, track patient recruitment, and ensure timely reporting of adverse events. The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field, with at least 3 years of experience as a Clinical Research Associate. Strong knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials is essential. Excellent organizational, communication, and interpersonal skills are required to effectively manage multiple sites and build strong relationships with site personnel. The ability to work independently, manage time effectively, and travel occasionally as needed (though the role is primarily remote) is important. This is a fantastic opportunity to advance your career in clinical research and contribute to the development of life-saving medications, supporting trials related to **Isa Town, Southern, BH**.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Senior cra Jobs in Bahrain !
6
Clinical Research Associate (CRA)
100 Al Ghurayfah
BHD80000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is actively seeking a highly skilled and motivated Clinical Research Associate (CRA) to join their on-site team. This pivotal role will involve overseeing and managing clinical trial sites, ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. Your responsibilities will include site initiation visits, ongoing monitoring visits, and close-out visits to assess study conduct, data integrity, and patient safety. You will serve as the primary liaison between the sponsor and investigative sites, providing training to site staff, resolving issues, and ensuring timely data collection and reporting. We are looking for an individual with a strong understanding of clinical trial processes, excellent communication and interpersonal skills, and the ability to travel as needed. Proven experience in site management, source data verification, and regulatory compliance is essential. A Bachelor's degree in a life science, nursing, or a related field is required. Advanced degrees or relevant certifications (e.g., ACRP, SoCRA) are a plus. A minimum of 3-5 years of experience as a CRA is expected. The ability to work independently and collaboratively within a team environment is crucial. This position is based at our facility in **Seef, Capital, BH**, and requires your regular presence. If you are a dedicated CRA looking to contribute to life-changing pharmaceutical research in a dynamic setting, we encourage you to apply.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate (CRA)
150 Riffa, Southern
BHD75000 Annually
WhatJobs
Posted 5 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company with a significant presence in Bahrain, is actively seeking a diligent and detail-oriented Clinical Research Associate (CRA) to join their dynamic team. This role is crucial for ensuring the successful execution of clinical trials in compliance with all regulatory requirements and ethical standards. The CRA will be responsible for site management, monitoring trial progress, and ensuring data integrity. This position offers a fantastic opportunity to contribute to the development of life-saving medications.
Responsibilities:
Qualifications:
This is a rewarding career path for individuals passionate about medical advancements and patient well-being. The role is based in Riffa, Southern, BH and offers a hybrid work model.
Responsibilities:
- Identify, evaluate, and select clinical trial sites, ensuring their suitability for participation.
- Initiate, monitor, and close out clinical trial sites according to study protocols and Good Clinical Practice (GCP) guidelines.
- Ensure adherence to study protocols, regulatory requirements, and data integrity standards.
- Conduct site visits (remote and on-site) to monitor study conduct, verify source data, and resolve discrepancies.
- Train and support investigators and site staff on study-related procedures and requirements.
- Manage study supplies and investigational product at trial sites.
- Review and process essential documents, ensuring accuracy and completeness.
- Communicate effectively with study sponsors, investigators, and regulatory authorities.
- Prepare and submit regulatory documents and reports as required.
- Identify and report adverse events and safety concerns promptly.
- Maintain accurate and up-to-date site files and databases.
- Contribute to the development and refinement of clinical trial protocols and procedures.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare discipline. A Master's degree is a plus.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical trial management role.
- Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience in site monitoring, data verification, and regulatory compliance.
- Excellent organizational and time management skills, with the ability to manage multiple priorities.
- Strong attention to detail and accuracy.
- Exceptional communication, interpersonal, and negotiation skills.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to travel to clinical trial sites as needed.
- Proficiency in English is essential; knowledge of Arabic is an advantage.
This is a rewarding career path for individuals passionate about medical advancements and patient well-being. The role is based in Riffa, Southern, BH and offers a hybrid work model.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate (CRA)
1030 Saar, Northern
BHD70000 Annually
WhatJobs
Posted 5 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a meticulous and dedicated Clinical Research Associate (CRA) to support their ongoing clinical trials. This hybrid role offers a balance of remote work flexibility and necessary on-site responsibilities, primarily focusing on sites in the Northern region. The CRA will be instrumental in ensuring the quality and integrity of clinical trial data by monitoring study conduct at investigational sites. This involves verifying compliance with protocol, regulations, and Good Clinical Practice (GCP) guidelines. The ideal candidate possesses a strong scientific background, excellent organizational skills, and a keen eye for detail.
Key Responsibilities:
Qualifications:
This hybrid position requires individuals who can effectively manage their time between remote tasks and on-site responsibilities at various clinical locations. Join our client's innovative team and play a crucial role in advancing pharmaceutical research and development.
Key Responsibilities:
- Conduct site visits (initiation, monitoring, and close-out) in accordance with study requirements and timelines.
- Verify the accuracy, completeness, and consistency of clinical data through source data verification (SDV).
- Ensure sites are in compliance with the study protocol, Good Clinical Practice (GCP), and all applicable regulatory requirements.
- Train and guide study site personnel on protocol, study procedures, and data collection.
- Manage and maintain study-related essential documents.
- Monitor subject recruitment and retention efforts at study sites.
- Identify, track, and resolve site-related issues and action items.
- Prepare and submit timely monitoring visit reports.
- Communicate effectively with investigators, site staff, and internal project teams.
- Contribute to the development and review of study documents, including protocols and case report forms (CRFs).
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline. A Master's degree is a plus.
- Minimum of 3-5 years of experience as a Clinical Research Associate.
- Comprehensive understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with various therapeutic areas is advantageous.
- Proficiency in Electronic Data Capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Ability to travel to clinical sites as needed.
- Problem-solving skills with a proactive approach.
- Familiarity with the healthcare landscape in Saar, Northern, BH .
This hybrid position requires individuals who can effectively manage their time between remote tasks and on-site responsibilities at various clinical locations. Join our client's innovative team and play a crucial role in advancing pharmaceutical research and development.
Is this job a match or a miss?
This advertiser has chosen not to accept applicants from your region.
9