426 Clinical Operations jobs in Bahrain
Clinical Operations Manager
10701 Busaiteen, Muharraq
BHD6500 Annually
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Our client is seeking a highly organized and compassionate Clinical Operations Manager to oversee the daily operations of their community health center located in Busaiteen, Muharraq, BH . This role is instrumental in ensuring the delivery of high-quality patient care and efficient service delivery within the community. The ideal candidate will possess strong leadership skills, a comprehensive understanding of healthcare regulations, and a passion for social care. You will be responsible for managing staff, optimizing workflows, implementing policies and procedures, and ensuring compliance with all relevant healthcare standards. This position requires a hands-on approach to problem-solving, exceptional communication skills, and the ability to foster a supportive and collaborative environment for both staff and patients. Your duties will include managing budgets, overseeing patient scheduling, coordinating with external healthcare providers, and ensuring the availability of necessary resources and supplies. You will also play a key role in quality improvement initiatives and patient satisfaction surveys. The successful candidate will contribute significantly to the positive impact our client has on the community's well-being. This is a vital role within the community and social care sector, offering a chance to make a real difference.
Key Responsibilities:
Key Responsibilities:
- Manage the day-to-day operations of the health center, ensuring efficient service delivery.
- Supervise and mentor clinical and administrative staff, fostering a positive work environment.
- Develop, implement, and enforce policies and procedures to maintain high standards of care.
- Ensure compliance with all healthcare regulations, licensing requirements, and accreditation standards.
- Oversee patient scheduling, registration, and record-keeping processes.
- Manage clinic budgets, track expenses, and ensure financial viability.
- Coordinate with physicians, nurses, and other healthcare professionals to optimize patient care.
- Maintain inventory of medical supplies and equipment, ensuring adequate stock levels.
- Implement and monitor quality improvement initiatives to enhance patient outcomes and satisfaction.
- Address patient concerns and resolve complaints effectively.
- Bachelor's degree in Healthcare Administration, Nursing, Public Health, or a related field. A Master's degree is preferred.
- Minimum of 5 years of experience in healthcare management or a related field.
- Proven experience in managing clinical staff and operations.
- In-depth knowledge of healthcare regulations and best practices.
- Strong understanding of patient care principles and community health needs.
- Excellent leadership, communication, and interpersonal skills.
- Proficiency in healthcare management software and electronic health records (EHR).
- Demonstrated ability to manage budgets and financial resources effectively.
- Problem-solving and decision-making capabilities.
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0
Clinical Operations Manager - Elderly Care
1070 Saar, Northern
BHD85000 Annually
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We are recruiting on behalf of our client for a dedicated and compassionate Clinical Operations Manager to lead our esteemed community care services in Saar, Northern, BH . This vital role involves the overall management and strategic development of our operations, focusing on delivering exceptional care and support to elderly individuals within their homes and community settings. The Clinical Operations Manager will be responsible for ensuring the highest standards of patient care, safety, and satisfaction. Key duties include overseeing the recruitment, training, and performance management of a multidisciplinary care team, including nurses, caregivers, and support staff. You will develop and implement care plans, ensuring they are person-centered and responsive to the evolving needs of our clients. Budget management, resource allocation, and ensuring compliance with all relevant healthcare regulations and industry best practices are crucial aspects of this position. The successful candidate will foster strong relationships with clients, their families, and external healthcare providers to ensure integrated and seamless care delivery. Innovation in service delivery and the adoption of new technologies to enhance care quality will be highly encouraged. A proactive approach to identifying and mitigating risks within the care environment is essential. Our client is committed to creating a supportive and professional working environment where staff can thrive. Essential qualifications include a degree in Nursing, Healthcare Management, or a related field. A postgraduate qualification in a relevant area is highly desirable. Significant experience (minimum 8 years) in a senior clinical or operational management role within the social care or healthcare sector, with a strong focus on elderly care, is mandatory. Proven leadership capabilities, excellent organizational and communication skills, and a deep understanding of the challenges and rewards of community-based care are required. This is a unique opportunity to shape the future of elder care in the region.
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1
Clinical Operations Manager, Community Health
10985 Seef, Capital
BHD85000 Annually
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Our client, a leading non-profit organization dedicated to improving community well-being, is seeking a highly motivated and experienced Clinical Operations Manager to oversee community health programs in Jidhafs, Capital, BH . This vital role is responsible for the efficient and effective delivery of essential healthcare services to vulnerable populations. You will manage daily clinical operations, supervise healthcare professionals (nurses, community health workers, social workers), and ensure the highest quality of patient care. Key responsibilities include developing and implementing operational policies and procedures, managing budgets, and ensuring compliance with healthcare regulations and standards. The ideal candidate will have a strong background in healthcare management, public health, or social work, coupled with excellent leadership and interpersonal skills. You will be instrumental in fostering strong relationships with community partners, government agencies, and funding bodies to expand service reach and impact. This position requires experience in program development, performance monitoring, and quality improvement initiatives. The ability to manage staff performance, provide training and support, and create a positive and supportive work environment is crucial. You will also be involved in data collection and analysis to report on program outcomes and identify areas for enhancement. A passion for social justice and a commitment to serving diverse communities are essential qualities for this role. This is an exceptional opportunity to make a tangible difference in the lives of individuals and families within the community.
Responsibilities:
Responsibilities:
- Oversee the daily operations of community health programs and clinics.
- Manage and supervise a multidisciplinary team of healthcare professionals.
- Ensure the delivery of high-quality, patient-centered care.
- Develop and implement operational policies, procedures, and workflows.
- Manage program budgets and resources effectively.
- Ensure compliance with all relevant healthcare regulations and standards.
- Monitor program performance and outcomes, implementing quality improvement initiatives.
- Build and maintain strong relationships with community stakeholders and partners.
- Coordinate patient referrals and linkages to other services.
- Provide training and professional development opportunities for staff.
- Bachelor's degree in Nursing, Public Health, Healthcare Administration, Social Work, or a related field. Master's degree preferred.
- Minimum of 5 years of experience in healthcare management or community health program leadership.
- Proven experience in supervising clinical or social service teams.
- Knowledge of community health principles, public health initiatives, and healthcare delivery systems.
- Experience with budget management and resource allocation.
- Familiarity with healthcare regulations (e.g., HIPAA) and quality improvement methodologies.
- Excellent leadership, communication, organizational, and interpersonal skills.
- Ability to work effectively with diverse populations and community stakeholders.
- Proficiency in EMR/EHR systems and Microsoft Office Suite.
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2
Clinical Research Associate - Oncology Trials
00780 Hamad Town, Northern
BHD70000 Annually
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Posted 1 day ago
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Our client is seeking a dedicated and meticulous Clinical Research Associate (CRA) to support their pioneering work in oncology clinical trials. This hybrid role offers a blend of remote work flexibility and essential on-site visits to healthcare facilities in and around Hamad Town, Northern, BH . As a CRA, you will play a crucial role in ensuring the quality, integrity, and accuracy of clinical trial data. Your responsibilities will include site initiation, monitoring, and close-out visits; verifying data accuracy against source documents; ensuring compliance with protocols, GCP guidelines, and regulatory requirements; and managing study-related documentation. You will also serve as a key liaison between the study sites, sponsors, and regulatory authorities.
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A minimum of 2-3 years of direct experience as a Clinical Research Associate, with a strong emphasis on oncology trials, is required. Thorough knowledge of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements for clinical trials is essential. Excellent organizational skills, attention to detail, and the ability to manage multiple priorities are paramount. Strong interpersonal and communication skills are necessary for building effective relationships with site staff and internal stakeholders. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This role is critical to advancing cancer research and requires a passionate commitment to patient safety and data integrity.
Key Responsibilities:
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. A minimum of 2-3 years of direct experience as a Clinical Research Associate, with a strong emphasis on oncology trials, is required. Thorough knowledge of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements for clinical trials is essential. Excellent organizational skills, attention to detail, and the ability to manage multiple priorities are paramount. Strong interpersonal and communication skills are necessary for building effective relationships with site staff and internal stakeholders. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is highly desirable. This role is critical to advancing cancer research and requires a passionate commitment to patient safety and data integrity.
Key Responsibilities:
- Conduct site visits for clinical trial monitoring.
- Ensure compliance with study protocols and regulatory guidelines.
- Verify accuracy and completeness of clinical trial data.
- Manage study documentation and site records.
- Train site staff on study-related procedures.
- Liaise between study sites, sponsors, and regulatory bodies.
- Resolve data discrepancies and site issues.
- Assist with site initiation and close-out procedures.
- Contribute to the overall quality of clinical research.
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3
Clinical Research Associate - Oncology Trials
2001 Saar, Northern
BHD85000 Annually
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Posted 2 days ago
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Our client, a leading pharmaceutical company at the forefront of cancer research, is seeking an experienced Clinical Research Associate (CRA) to join their prestigious team. This role is fully remote, allowing you to contribute to life-saving clinical trials from the comfort of your home. As a CRA, you will be responsible for monitoring and managing clinical trials in accordance with Good Clinical Practice (GCP) guidelines and regulatory requirements. Your primary focus will be on ensuring the quality, accuracy, and integrity of data collected during oncology studies. This will involve site initiation visits, routine monitoring visits, and close-out visits at clinical trial sites. You will liaise directly with investigators and site staff, providing essential support and ensuring adherence to study protocols. A deep understanding of pharmaceutical regulations, clinical trial processes, and therapeutic areas, particularly oncology, is essential. Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS) is required. The ideal candidate will possess excellent analytical skills, meticulous attention to detail, and the ability to work independently and manage multiple priorities effectively in a remote setting. Strong communication and interpersonal skills are vital for building rapport with study sites and internal teams. We are looking for individuals with a proven track record of successful clinical trial monitoring and a passion for advancing cancer therapies. A Bachelor's degree in a life science, nursing, or a related field is required, along with significant experience as a CRA. This is a demanding yet highly rewarding role where you can directly impact the development of new treatments for patients battling cancer. If you are driven by scientific advancement and committed to ethical research practices, we invite you to apply.
Responsibilities:
Responsibilities:
- Monitor clinical trial activities at assigned sites to ensure compliance with protocols, GCP, and regulatory standards.
- Initiate, monitor, and close out clinical trial sites.
- Verify the accuracy and completeness of clinical trial data through source data verification.
- Ensure proper documentation and record-keeping at study sites.
- Communicate effectively with investigators, site staff, and study sponsors.
- Identify and resolve issues related to study conduct and data quality.
- Train site personnel on study protocols and procedures.
- Prepare monitoring visit reports and follow up on action items.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Experience in oncology clinical trials is strongly preferred.
- Proficiency in EDC, CTMS, and other clinical trial management software.
- Excellent analytical, problem-solving, and organizational skills.
- Strong written and verbal communication abilities.
- Ability to travel to sites as required (though this role is remote, occasional site visits may be needed).
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4
Clinical Research Associate - Pharmaceutical Trials
66778 Diplomatic Area
BHD70000 Annually
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Posted 4 days ago
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Our client, a prominent pharmaceutical company, is seeking a meticulous and dedicated Clinical Research Associate (CRA) to contribute to groundbreaking drug development. This role is vital for ensuring the quality, integrity, and ethical conduct of clinical trials across various therapeutic areas. The ideal candidate will have a strong background in life sciences, a thorough understanding of Good Clinical Practice (GCP) guidelines, and experience in monitoring clinical trial sites. You will be responsible for site selection and initiation, regular monitoring visits, data verification, and ensuring compliance with study protocols and regulatory requirements. Key duties include managing investigational product, maintaining study documentation, communicating effectively with investigators and site staff, and resolving site-specific issues. The CRA will play a crucial role in data collection and reporting, contributing to the successful completion of clinical studies. Excellent organizational skills, attention to detail, and the ability to travel as needed are essential. This challenging and rewarding opportunity is based in **Isa Town, Southern, BH**, offering a chance to be at the forefront of pharmaceutical innovation. We are looking for individuals passionate about clinical research, committed to patient safety, and driven to advance medical treatments.
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5
Clinical Research Associate - Oncology Trials
00130 Seef, Capital
BHD95000 Annually
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Posted 4 days ago
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Our client, a leading biopharmaceutical company dedicated to advancing cancer treatments, is seeking a highly motivated Clinical Research Associate (CRA) to support critical oncology trials from their site in **Jidhafs, Capital, BH**. In this vital role, you will be responsible for monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and good clinical practices (GCP). Your efforts will directly contribute to the successful development of life-saving therapies. You will work closely with investigators, site staff, and internal study teams to ensure the quality and integrity of trial data. Responsibilities will encompass:
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline. A minimum of 3 years of experience as a CRA, with a strong focus on oncology clinical trials, is required. Thorough knowledge of ICH-GCP guidelines and regulatory requirements is essential. Excellent organizational, time management, and problem-solving skills are necessary. Strong verbal and written communication abilities, coupled with proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems, are highly desirable. This is a challenging yet rewarding opportunity to contribute to groundbreaking medical research and career advancement in the pharmaceutical industry.
- Performing site initiation visits, interim monitoring visits, and close-out visits according to established plans.
- Ensuring that clinical trial activities are conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), and applicable regulations.
- Verifying the accuracy, completeness, and consistency of source documents and case report forms (CRFs).
- Reviewing and verifying patient eligibility and informed consent process.
- Managing drug accountability and ensuring proper storage and handling of investigational products.
- Identifying and addressing potential risks and issues at trial sites.
- Communicating effectively with investigators and site staff, providing training and support as needed.
- Maintaining comprehensive trial documentation and ensuring timely data entry.
- Reporting study progress, site issues, and deviations to the Clinical Study Manager.
The ideal candidate will possess a Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline. A minimum of 3 years of experience as a CRA, with a strong focus on oncology clinical trials, is required. Thorough knowledge of ICH-GCP guidelines and regulatory requirements is essential. Excellent organizational, time management, and problem-solving skills are necessary. Strong verbal and written communication abilities, coupled with proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems, are highly desirable. This is a challenging yet rewarding opportunity to contribute to groundbreaking medical research and career advancement in the pharmaceutical industry.
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6
Clinical Research Associate - Pharmaceutical Trials
10304 Zallaq, Southern
BHD75000 Annually
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Posted 10 days ago
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Our client, a global leader in pharmaceutical development, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to support its ongoing clinical trials. This vital role involves overseeing the progress of clinical studies at investigational sites, ensuring adherence to the study protocol, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. The CRA will be responsible for site selection, initiation, monitoring, and close-out visits, as well as managing data collection and integrity. Key responsibilities include verifying the accuracy and completeness of source data, ensuring proper informed consent procedures are followed, and addressing any site-specific issues that may arise. You will serve as the primary point of contact between the sponsor and the investigational sites, fostering strong working relationships with investigators and site staff. The successful candidate will also assist in the preparation of regulatory submission documents and contribute to the overall success of the clinical development program. A Bachelor's degree in a life science, nursing, or a related healthcare field is required. Previous experience as a CRA or in a similar clinical research role (minimum 2-3 years) is essential, with a strong understanding of clinical trial phases, regulatory affairs, and data management. Excellent knowledge of ICH-GCP guidelines and FDA regulations is mandatory. Strong organizational, communication, and interpersonal skills are crucial for effective site management and stakeholder interaction. The ability to travel to investigational sites as required and a commitment to maintaining data quality and patient safety are paramount. This contract position is based in **Zallaq, Southern, BH**, offering a competitive hourly rate and the opportunity to gain valuable experience in cutting-edge pharmaceutical research.
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7
Clinical Research Associate - Pharmaceutical Trials
701 Southern, Southern
BHD80000 Annually
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Posted 10 days ago
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Our client, a prominent pharmaceutical research organization, is seeking a highly organized and diligent Clinical Research Associate (CRA) to support their ongoing clinical trials in Nuwaidrat, Southern, BH . This critical role ensures that clinical trials are conducted according to protocol, Good Clinical Practice (GCP) guidelines, and all applicable regulatory requirements. The ideal candidate will have a strong understanding of clinical trial processes, data management, and regulatory compliance. Responsibilities include site initiation, monitoring, and close-out visits; ensuring the accurate and timely collection of clinical data; verifying source documentation; managing investigational product accountability; and serving as the primary liaison between study sites and the clinical research team. You will be responsible for identifying and resolving any issues or discrepancies that arise during trial conduct. Excellent interpersonal skills, attention to detail, and the ability to communicate effectively with healthcare professionals are essential. A background in nursing, life sciences, or a related field, along with previous experience as a CRA or in a similar clinical research role, is required. Knowledge of ICH-GCP and relevant regulatory requirements is crucial. This position offers a competitive salary, benefits, and the opportunity to work on impactful clinical research projects that contribute to the development of new medicines. Join our dedicated team and play a key role in bringing life-changing therapies to patients.
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8
Clinical Research Associate
50000 Busaiteen, Muharraq
BHD2500 month
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Posted 1 day ago
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Our client, a prominent pharmaceutical company with operations in **A'ali, Northern, BH**, is looking for a meticulous and dedicated Clinical Research Associate (CRA) to contribute to their groundbreaking drug development programs. As a CRA, you will play a vital role in ensuring the quality and integrity of clinical trials, adhering to strict protocols and regulatory guidelines. Your primary responsibilities will include monitoring clinical trial sites, ensuring accurate data collection and reporting, and verifying that trials are conducted in compliance with Good Clinical Practice (GCP) and other relevant regulations. You will be responsible for site initiation visits, routine monitoring visits, and close-out visits, as well as managing study documentation and resolving data queries. Building and maintaining strong relationships with investigators, site staff, and study sponsors is crucial for the success of the trials. The ideal candidate will possess a strong understanding of clinical trial processes, medical terminology, and regulatory requirements within the pharmaceutical industry. Excellent attention to detail, strong organizational and communication skills, and the ability to work independently and as part of a team are essential. A Bachelor's degree in a life science or healthcare-related field, along with previous experience as a CRA or in a related clinical research role, is highly preferred. This is an excellent opportunity for an experienced professional to make a significant contribution to advancing healthcare through rigorous clinical research.
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