428 Senior Cra jobs in Bahrain
Clinical Research Associate (CRA)
00710 Seef, Capital
BHD90000 Annually
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Job Description
Our client is a prominent pharmaceutical company looking for a dedicated Clinical Research Associate (CRA) to oversee and manage their clinical trials. The CRA will be responsible for ensuring that trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. This role involves frequent travel to study sites within the region to monitor trial progress, ensure data accuracy, and verify patient safety. Strong organizational skills and meticulous attention to detail are paramount.
Responsibilities:
Qualifications:
Responsibilities:
- Monitor clinical trial activities at investigative sites to ensure adherence to protocol, SOPs, and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical trial data through source data verification (SDV).
- Ensure patient safety and rights are protected throughout the trial.
- Build and maintain positive relationships with site staff, investigators, and study sponsors.
- Conduct pre-study, initiation, interim monitoring, and close-out visits at clinical sites.
- Identify, document, and resolve site-specific issues and discrepancies.
- Train site staff on study procedures and data collection requirements.
- Ensure investigational product is handled, dispensed, and accounted for correctly.
- Prepare and present monitoring visit reports.
- Assist in the preparation and submission of regulatory documents.
- Ensure timely enrollment of subjects and troubleshoot recruitment challenges.
- Maintain all necessary trial documentation and ensure site compliance.
Qualifications:
- Bachelor's degree in a life science, nursing, or related field; Master's degree preferred.
- Minimum of 3 years of experience as a Clinical Research Associate, preferably with a CRO or pharmaceutical company.
- Thorough understanding of ICH-GCP guidelines and other relevant regulatory requirements.
- Experience in monitoring Phase I-IV clinical trials.
- Excellent written and verbal communication skills.
- Strong organizational and time management skills.
- Proficiency in MS Office Suite and clinical trial management systems (CTMS).
- Ability to travel frequently to clinical sites (up to 75%).
- Detail-oriented with strong analytical and problem-solving skills.
- Ability to work independently and as part of a team.
- CRA certification is a plus.
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0
Clinical Research Associate (CRA)
225 Manama, Capital
BHD70000 Annually
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Job Description
Our client, a renowned pharmaceutical company dedicated to advancing healthcare, is looking for a diligent and experienced Clinical Research Associate (CRA) to join their clinical operations team. This role involves monitoring and managing clinical trials at various investigator sites to ensure data accuracy, patient safety, and compliance with protocols and regulatory guidelines. The position offers a hybrid work model, combining remote responsibilities with on-site visits.
Responsibilities:
Qualifications:
This vital role is based in Manama, Capital, BH , offering a competitive compensation package, comprehensive benefits, and significant career growth opportunities within the pharmaceutical industry.
Responsibilities:
- Conduct site visits (initiation, interim, close-out) to assess patient eligibility, ensure protocol compliance, and verify data accuracy.
- Monitor study conduct and data collection processes to ensure adherence to Good Clinical Practice (GCP) and relevant regulations.
- Train and support investigators and site staff on study protocols, procedures, and regulatory requirements.
- Manage and review essential regulatory documents, ensuring completeness and accuracy.
- Oversee drug accountability and investigational product management at study sites.
- Identify and report adverse events and safety information in a timely manner.
- Prepare monitoring reports and communicate findings and recommendations to the study team and site personnel.
- Ensure timely resolution of site issues and discrepancies.
- Collaborate with study sponsors, CROs, and investigators to ensure efficient trial progress.
- Maintain effective communication with all stakeholders involved in the clinical trial.
- Contribute to the development and review of study-related documents, including protocols and case report forms (CRFs).
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline. Advanced degree preferred.
- 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 other relevant regulatory requirements.
- Experience with various therapeutic areas is desirable.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong organizational, analytical, and problem-solving skills.
- Excellent written and verbal communication abilities.
- Ability to travel to study sites as required (estimated 40-60% travel).
- Demonstrated ability to work independently and manage multiple priorities effectively in a hybrid work environment.
This vital role is based in Manama, Capital, BH , offering a competitive compensation package, comprehensive benefits, and significant career growth opportunities within the pharmaceutical industry.
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1
Clinical Research Associate (CRA)
20709 Manama, Capital
BHD90000 Annually
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Job Description
Our client, a leading pharmaceutical company renowned for its commitment to advancing healthcare, is seeking a diligent and experienced Clinical Research Associate (CRA) for a hybrid role. You will play a vital role in ensuring the successful execution of clinical trials by monitoring study sites, ensuring data integrity, and maintaining compliance with regulatory standards and protocols. This position requires a balance of on-site visits to clinical sites and remote data review and management, offering a dynamic work environment. Your expertise will be critical in bringing life-saving treatments to patients.
Key Responsibilities:
Qualifications:
This hybrid role offers a competitive compensation package and the opportunity to contribute significantly to groundbreaking clinical research.
Key Responsibilities:
- Monitor assigned clinical trial sites to ensure compliance with study protocols, GCP, and regulatory requirements.
- Perform site initiation visits, interim monitoring visits, and study close-out visits.
- Verify the accuracy, completeness, and validity of clinical trial data by reviewing source documents and case report forms (CRFs).
- Ensure proper drug accountability and investigational product management at study sites.
- Identify, resolve, and document site-specific issues and deviations.
- Train and support site staff on study procedures, data entry, and regulatory requirements.
- Communicate effectively with investigators, study coordinators, and other site personnel.
- Prepare and submit monitoring visit reports in a timely manner.
- Ensure timely retrieval and reconciliation of study-related documents.
- Identify potential risks to study timelines and data integrity and implement corrective actions.
- Contribute to the development and review of study-related documents, such as protocols and CRFs.
- Maintain all study documentation and ensure proper archiving.
- Adhere to all company policies and procedures.
- Participate in investigator meetings and training sessions.
- Manage relationships with clinical sites and key opinion leaders.
Qualifications:
- Bachelor's degree in a life science, nursing, or related field.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA) or similar role.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Strong understanding of medical terminology and clinical trial processes.
- Excellent organizational, time management, and problem-solving skills.
- Exceptional written and verbal communication skills.
- Ability to travel to clinical sites as required.
- Proficiency in Microsoft Office Suite.
- Ability to work independently and collaboratively in a hybrid work environment.
- Experience in a specific therapeutic area (e.g., oncology, cardiology) is a plus.
This hybrid role offers a competitive compensation package and the opportunity to contribute significantly to groundbreaking clinical research.
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate (CRA)
14256 Riffa, Southern
BHD90000 Annually
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Job Description
Our client, a leading Pharmaceutical company, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their clinical development team. This is an office-based role, though occasional travel to clinical sites within the region may be required. The CRA will be responsible for monitoring clinical trials to ensure they are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and applicable regulations (e.g., GCP, FDA). You will play a critical role in ensuring the quality and integrity of clinical trial data and protecting the rights and well-being of study participants.
Responsibilities:
Responsibilities:
- Perform site initiation visits, interim monitoring visits, and close-out visits according to study requirements.
- Verify the accuracy, completeness, and quality of source documents and trial data at investigational sites.
- Ensure compliance with the study protocol, SOPs, and regulatory requirements.
- Act as a liaison between the sponsor and the investigational sites, providing support and training to site staff.
- Review and track regulatory documents, including essential trial documents.
- Oversee drug accountability and investigational product management at sites.
- Identify, document, and escalate potential issues or deviations from protocol and SOPs.
- Participate in study team meetings and contribute to the development of study-related documents.
- Ensure site personnel are properly trained on the study protocol and investigational product.
- Manage site communication and problem resolution effectively.
- Bachelor's degree in a life science, nursing, or a related scientific discipline.
- Minimum of 3-5 years of experience as a Clinical Research Associate (CRA).
- Thorough understanding of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Experience in monitoring clinical trials across various therapeutic areas.
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent organizational, time management, and problem-solving skills.
- Strong communication and interpersonal skills, with the ability to build rapport with site personnel.
- Ability to travel as needed to assigned clinical sites.
- Detail-oriented with a commitment to data accuracy and patient safety.
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3
Clinical Research Associate (CRA)
30320 Busaiteen, Muharraq
BHD80000 Annually
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Posted 1 day ago
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Job Description
Our client is seeking a diligent and organized Clinical Research Associate (CRA) to contribute to critical clinical trials based in A'ali, Northern, BH . This role is pivotal in ensuring the quality and integrity of clinical trial data by monitoring study sites and verifying compliance with protocols and regulations. As a CRA, you will be responsible for site initiation, routine monitoring visits, and study close-out activities, ensuring that all research is conducted according to Good Clinical Practice (GCP) guidelines and applicable regulatory standards.
Your responsibilities will include:
The ideal candidate will hold a Bachelor's degree in a life science, nursing, or a related field, with at least 3 years of experience as a CRA or in a similar clinical research role. A strong understanding of ICH-GCP guidelines and relevant regulatory requirements (e.g., FDA, EMA) is mandatory. Excellent interpersonal, organizational, and problem-solving skills are essential, as is proficiency in clinical trial management software and EDC systems. The ability to travel extensively to study sites within the region is required for this position in A'ali, Northern, BH . This is an excellent opportunity for a dedicated professional to advance their career in clinical research and contribute to the successful execution of vital medical studies.
Your responsibilities will include:
- Performing on-site and remote monitoring visits to assess study conduct and regulatory compliance.
- Verifying the accuracy, completeness, and validity of clinical trial data through source data verification (SDV).
- Ensuring investigational products are properly stored, dispensed, and accounted for.
- Identifying and reporting adverse events and protocol deviations in a timely manner.
- Training site staff on study protocols and procedures.
- Building and maintaining strong relationships with investigators and study site personnel.
- Resolving data discrepancies and ensuring accurate and timely query resolution.
- Preparing monitoring reports and providing feedback to study teams.
- Assisting with regulatory submissions and audits.
The ideal candidate will hold a Bachelor's degree in a life science, nursing, or a related field, with at least 3 years of experience as a CRA or in a similar clinical research role. A strong understanding of ICH-GCP guidelines and relevant regulatory requirements (e.g., FDA, EMA) is mandatory. Excellent interpersonal, organizational, and problem-solving skills are essential, as is proficiency in clinical trial management software and EDC systems. The ability to travel extensively to study sites within the region is required for this position in A'ali, Northern, BH . This is an excellent opportunity for a dedicated professional to advance their career in clinical research and contribute to the successful execution of vital medical studies.
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4
Clinical Research Associate (CRA)
905 Seef, Capital
BHD80000 Annually
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Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their team in Jidhafs. This role offers a hybrid work arrangement, combining remote flexibility with essential on-site responsibilities. The CRA will play a crucial role in ensuring the smooth and efficient execution of clinical trials, adhering to Good Clinical Practice (GCP) guidelines and regulatory requirements. Your primary responsibilities will include site selection, initiation, monitoring, and close-out visits. You will be responsible for verifying the accuracy and completeness of clinical trial data, ensuring patient safety, and confirming compliance with protocols and regulatory standards. This involves performing source data verification, reviewing essential documents, and addressing any discrepancies that may arise. The ideal candidate will possess excellent communication, interpersonal, and organizational skills, with a strong ability to build rapport with investigators and site staff. A Bachelor's degree in a life science, nursing, or a related field is required. Previous experience as a CRA or in a similar clinical research role is essential, with a solid understanding of clinical trial phases and methodologies. You must be proficient in using clinical trial management systems and electronic data capture (EDC) systems. Travel to clinical trial sites will be a necessary component of this role. The ability to manage multiple projects simultaneously, prioritize tasks effectively, and work independently with minimal supervision is key to success. If you are passionate about advancing medical research and contributing to the development of life-saving therapies, this is an excellent opportunity to grow your career in a supportive and collaborative environment.
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5
Clinical Research Associate (CRA)
20212 Al Jasra
BHD85000 Annually
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Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical company, is looking for an experienced Clinical Research Associate (CRA) to support their vital clinical trials. This role offers a hybrid work model, blending remote flexibility with occasional on-site engagement. As a CRA, you will play a crucial role in ensuring the quality and integrity of clinical trial data. Your responsibilities will include site selection, initiation, monitoring, and close-out visits to ensure adherence to protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. You will be responsible for source data verification, patient recruitment support, and maintaining essential trial documentation. Excellent interpersonal and communication skills are essential for building strong relationships with investigators, site staff, and study participants. A Bachelor's degree in a life science, nursing, or a related field is required, along with a minimum of 3 years of experience as a CRA or in a similar clinical research role. Knowledge of regulatory requirements (FDA, EMA) and ICH-GCP is a must. The ability to manage multiple projects simultaneously and travel to clinical sites as needed is also important. This position offers a fantastic opportunity to contribute to the development of life-saving medications and advance your career in the pharmaceutical industry. The role is primarily based out of Hidd, Muharraq, BH , with a hybrid working arrangement.
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6
Clinical Research Associate (CRA)
601 Muharraq, Muharraq
BHD60000 Annually
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Posted 2 days ago
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Job Description
Our client is seeking a highly skilled and motivated Clinical Research Associate (CRA) to support their pharmaceutical research initiatives in **Muharraq, Muharraq, BH**. This vital role involves monitoring clinical trials to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits, as well as data verification and ensuring the accuracy and integrity of trial information.
Key responsibilities include ensuring that trials are conducted ethically and in accordance with study protocols, identifying and reporting adverse events, and maintaining effective communication with investigators, site staff, and internal project teams. You will play a crucial part in the drug development process, contributing to the advancement of new pharmaceutical treatments. The ideal candidate will possess a strong background in life sciences, a Bachelor's degree in a relevant field (e.g., Pharmacy, Biology, Nursing), and prior experience in clinical trial monitoring. Excellent understanding of regulatory guidelines (e.g., FDA, EMA) and strong analytical and organizational skills are mandatory.
This position requires individuals who are detail-oriented, possess excellent problem-solving abilities, and can work independently while traveling to different clinical sites. Effective communication and interpersonal skills are essential for building strong relationships with research sites and internal stakeholders. The ability to manage multiple trials and prioritize tasks effectively is crucial for success. Join our client's team and contribute to bringing life-saving medications to patients worldwide.
Key responsibilities include ensuring that trials are conducted ethically and in accordance with study protocols, identifying and reporting adverse events, and maintaining effective communication with investigators, site staff, and internal project teams. You will play a crucial part in the drug development process, contributing to the advancement of new pharmaceutical treatments. The ideal candidate will possess a strong background in life sciences, a Bachelor's degree in a relevant field (e.g., Pharmacy, Biology, Nursing), and prior experience in clinical trial monitoring. Excellent understanding of regulatory guidelines (e.g., FDA, EMA) and strong analytical and organizational skills are mandatory.
This position requires individuals who are detail-oriented, possess excellent problem-solving abilities, and can work independently while traveling to different clinical sites. Effective communication and interpersonal skills are essential for building strong relationships with research sites and internal stakeholders. The ability to manage multiple trials and prioritize tasks effectively is crucial for success. Join our client's team and contribute to bringing life-saving medications to patients worldwide.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate (CRA)
255 Seef, Capital
BHD65000 Annually
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Posted 2 days ago
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Job Description
Our client, a pioneering pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their esteemed team. This role is integral to the successful execution of clinical trials, ensuring compliance with regulatory standards and protocols. The CRA will be responsible for monitoring clinical trial sites, verifying data accuracy, ensuring patient safety, and maintaining accurate study documentation. You will work closely with investigators, site staff, and study sponsors to facilitate the smooth progression of research studies. This position is based in Jidhafs, Capital, BH and requires regular on-site visits to trial locations.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct site selection visits and qualification of potential investigators.
- Initiate clinical trial sites, ensuring all essential documents are in place and regulatory requirements are met.
- Monitor assigned clinical trial sites regularly to verify that the trial is conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements.
- Ensure patient safety and adherence to protocol through close monitoring of study procedures and source data verification.
- Manage investigational product accountability at the sites.
- Train site staff on study procedures and protocol requirements.
- Identify and report any deviations, adverse events, and serious adverse events promptly.
- Maintain accurate and complete trial documentation, including source documents, case report forms (CRFs), and trial master files (TMF).
- Build and maintain strong working relationships with investigators, site staff, and study sponsors.
- Participate in study team meetings and provide updates on site performance.
- Close-out clinical trial sites upon completion of the study.
- Ensure timely submission of all required study documents to the sponsor.
Qualifications:
- Bachelor's degree in a life science, nursing, pharmacy, or a related field.
- Proven experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
- Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements.
- Excellent knowledge of clinical trial processes and documentation.
- Strong analytical and problem-solving skills.
- Exceptional attention to detail and accuracy.
- Effective communication, interpersonal, and organizational skills.
- Ability to travel to clinical trial sites as required.
- Proficiency in clinical trial management software and electronic data capture systems.
- A commitment to patient safety and data integrity.
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8
Clinical Research Associate (CRA)
10200 Al Hidd
BHD70000 Annually
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Posted 2 days ago
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Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated Clinical Research Associate (CRA) to contribute to their innovative drug development programs. This hybrid role will involve a mix of site visits and remote monitoring. You will be responsible for monitoring clinical trial sites to ensure compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. Your duties will include site initiation visits, routine monitoring visits, close-out visits, reviewing case report forms (CRFs), and ensuring the accuracy and completeness of clinical data. You will also serve as a key liaison between the investigative sites and the sponsor, providing support to investigators and study staff. The ideal candidate will possess strong knowledge of clinical trial processes, regulatory requirements, and medical terminology. Excellent communication, organizational, and time-management skills are essential. A Bachelor's degree in a life science, nursing, or a related field is required, along with at least 2-3 years of experience as a CRA or in a similar clinical research role. Experience with various therapeutic areas is a plus. Certification from a recognized professional body is desirable. This is an excellent opportunity to join a growing team and make a significant contribution to bringing life-changing medicines to patients. You will work in a collaborative environment that values scientific rigor and patient safety.
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