1 210 Pharmaceuticals jobs in Bahrain
Senior Research Scientist - Pharmaceuticals
205 Busaiteen, Muharraq
BHD110000 Annually
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Our client, a leading pharmaceutical company, is looking for a talented Senior Research Scientist to join their innovative R&D team in Busaiteen, Muharraq, BH . This role is critical in driving the discovery and development of novel therapeutic agents. The ideal candidate will have a strong background in pharmaceutical research, extensive experience in drug discovery methodologies, and a passion for advancing patient care through scientific innovation.
Responsibilities:
Responsibilities:
- Design and execute experiments to identify and validate new drug targets.
- Conduct in-depth research on novel therapeutic compounds and modalities.
- Develop and optimize assays for high-throughput screening and lead optimization.
- Analyze experimental data, interpret results, and generate comprehensive reports.
- Collaborate with internal and external research partners to advance drug discovery programs.
- Contribute to the development of research strategies and project planning.
- Stay current with scientific literature and emerging trends in pharmaceutical research.
- Present research findings at scientific conferences and internal meetings.
- Mentor junior scientists and provide technical guidance.
- Ensure compliance with laboratory safety standards and regulatory guidelines.
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 7 years of post-doctoral research experience in the pharmaceutical industry or academia.
- Proven track record of success in drug discovery and development.
- Extensive experience with various laboratory techniques, including cell culture, molecular biology, and biochemical assays.
- Proficiency in data analysis software (e.g., GraphPad Prism, R).
- Strong understanding of disease mechanisms and therapeutic strategies.
- Excellent written and oral communication skills.
- Ability to work independently and collaboratively in a fast-paced research environment.
- Demonstrated leadership skills and experience in managing research projects.
- Passion for science and commitment to advancing human health.
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0
Quality Assurance Manager - Pharmaceuticals
51211 Hamad Town, Northern
BHD70000 Annually
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Our client is a leading pharmaceutical manufacturer committed to producing high-quality, safe, and effective medications. We are seeking a meticulous and experienced Quality Assurance Manager to oversee our comprehensive quality management systems at our advanced facility in Hamad Town, Northern, BH . This role is critical for ensuring regulatory compliance and maintaining the integrity of our pharmaceutical products.
The Quality Assurance Manager will be responsible for developing, implementing, and maintaining all quality assurance policies, procedures, and systems in accordance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards. Your duties will include overseeing quality control testing, managing batch release processes, conducting internal audits, investigating deviations and non-conformances, and implementing corrective and preventive actions (CAPA). You will also be responsible for training QA personnel, managing the documentation system, and ensuring that all manufacturing and laboratory activities meet stringent quality requirements. Collaboration with regulatory affairs, production, and R&D departments will be essential to uphold our commitment to quality.
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A minimum of 6 years of progressive experience in Quality Assurance within the pharmaceutical industry is required, with at least 3 years in a management or supervisory role. In-depth knowledge of GMP, FDA regulations, and other relevant pharmaceutical quality standards is essential. Strong analytical, problem-solving, and decision-making skills are paramount. You should have experience in audit management, deviation investigations, CAPA implementation, and quality risk management. Excellent leadership, communication, and interpersonal skills are necessary for effectively managing the QA team and interacting with other departments and regulatory agencies. If you are dedicated to ensuring product quality and patient safety, this is an exceptional opportunity.
Responsibilities:
The Quality Assurance Manager will be responsible for developing, implementing, and maintaining all quality assurance policies, procedures, and systems in accordance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards. Your duties will include overseeing quality control testing, managing batch release processes, conducting internal audits, investigating deviations and non-conformances, and implementing corrective and preventive actions (CAPA). You will also be responsible for training QA personnel, managing the documentation system, and ensuring that all manufacturing and laboratory activities meet stringent quality requirements. Collaboration with regulatory affairs, production, and R&D departments will be essential to uphold our commitment to quality.
The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A minimum of 6 years of progressive experience in Quality Assurance within the pharmaceutical industry is required, with at least 3 years in a management or supervisory role. In-depth knowledge of GMP, FDA regulations, and other relevant pharmaceutical quality standards is essential. Strong analytical, problem-solving, and decision-making skills are paramount. You should have experience in audit management, deviation investigations, CAPA implementation, and quality risk management. Excellent leadership, communication, and interpersonal skills are necessary for effectively managing the QA team and interacting with other departments and regulatory agencies. If you are dedicated to ensuring product quality and patient safety, this is an exceptional opportunity.
Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS).
- Ensure compliance with GMP, GLP, and other relevant pharmaceutical regulations.
- Oversee quality control procedures and batch release processes.
- Conduct internal audits and support external regulatory inspections.
- Investigate deviations, non-conformances, and customer complaints.
- Implement and track Corrective and Preventive Actions (CAPA).
- Manage product quality documentation and records.
- Train QA personnel and foster a quality-focused culture.
- Collaborate with production, R&D, and regulatory affairs departments.
- Monitor and evaluate supplier quality.
- Bachelor's or Master's degree in Pharmacy, Chemistry, or related science.
- Minimum 6 years of QA experience in the pharmaceutical industry.
- Proven experience in GMP and regulatory compliance.
- Strong knowledge of quality control and assurance methodologies.
- Experience with audits, deviations, and CAPA.
- Excellent leadership and team management skills.
- Strong analytical and problem-solving capabilities.
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1
Senior Process Engineer - Pharmaceuticals
900 Askar, Southern
BHD95000 Annually
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Our client, a leading pharmaceutical manufacturing company, is seeking an experienced Senior Process Engineer to oversee and optimize production processes at our facility in Tubli, Capital, BH . This role is crucial for ensuring the efficiency, quality, and safety of our pharmaceutical manufacturing operations, adhering to stringent regulatory standards. The ideal candidate will have a strong background in chemical or mechanical engineering with specialized knowledge in pharmaceutical production and process validation.
Responsibilities:
Responsibilities:
- Design, develop, and optimize manufacturing processes for pharmaceutical products, ensuring compliance with GMP (Good Manufacturing Practices) and other regulatory requirements.
- Troubleshoot and resolve process-related issues, identifying root causes and implementing corrective actions to minimize downtime and improve yield.
- Develop and execute process validation protocols and reports for new and existing manufacturing processes.
- Lead process improvement initiatives aimed at increasing efficiency, reducing costs, and enhancing product quality.
- Collaborate with R&D, Quality Assurance, and Production teams to ensure successful scale-up and transfer of new products and processes.
- Prepare process documentation, including Standard Operating Procedures (SOPs), batch records, and equipment specifications.
- Conduct process hazard analyses (PHAs) and implement safety measures to ensure a safe working environment.
- Train and mentor junior engineers and production personnel on process operations and best practices.
- Stay current with industry advancements in pharmaceutical manufacturing technology and regulatory changes.
- Manage capital projects related to process equipment upgrades and installations.
- Monitor process performance using statistical methods and recommend adjustments as needed.
- Bachelor's or Master's degree in Chemical Engineering, Mechanical Engineering, or a related field.
- Minimum of 6 years of experience in process engineering within the pharmaceutical or biotechnology industry.
- In-depth knowledge of pharmaceutical manufacturing processes (e.g., fermentation, purification, formulation, aseptic processing).
- Strong understanding of GMP, FDA regulations, and other relevant industry standards.
- Experience with process validation, IQ/OQ/PQ.
- Proficiency in process simulation software and data analysis tools.
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong project management and leadership abilities.
- Effective communication and interpersonal skills, with the ability to collaborate across departments.
- Experience with Lean Manufacturing or Six Sigma methodologies is a plus.
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2
Senior Research Scientist - Pharmaceuticals
00345 Northern, Northern
BHD90000 Annually
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Our client, a prominent pharmaceutical company, is seeking a highly skilled Senior Research Scientist to join their innovative R&D department in **Shakhura, Northern, BH**. This critical role involves designing and conducting complex experiments, analyzing data, and contributing to the discovery and development of novel therapeutic agents. The ideal candidate will have a strong background in pharmaceutical research, excellent analytical skills, and a passion for advancing medical science.
Responsibilities:
Responsibilities:
- Lead and execute research projects focused on drug discovery and development.
- Design and perform in vitro and in vivo experiments to evaluate compound efficacy and safety.
- Develop and validate new assays and experimental protocols.
- Analyze and interpret experimental data, drawing scientifically sound conclusions.
- Prepare detailed research reports, manuscripts for publication, and presentations for scientific conferences.
- Collaborate with cross-functional teams, including chemists, pharmacologists, and toxicologists.
- Contribute to the intellectual property portfolio through patent filings.
- Maintain laboratory equipment and ensure compliance with safety and regulatory guidelines.
- Mentor junior scientists and research associates.
- Stay abreast of the latest scientific literature and advancements in relevant therapeutic areas.
- Contribute to the strategic planning of research initiatives.
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 7 years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
- Proven track record of successful drug discovery or development projects.
- Extensive experience with various laboratory techniques, including cell culture, molecular biology assays, and animal models.
- Strong understanding of drug discovery processes and regulatory requirements.
- Excellent data analysis, problem-solving, and critical thinking skills.
- Proficient in scientific writing and presentation.
- Experience with high-throughput screening (HTS) is a plus.
- Demonstrated ability to lead research projects and manage scientific teams.
- Excellent communication and teamwork abilities.
- Knowledge of relevant therapeutic areas (e.g., oncology, immunology).
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3
Senior Research Scientist (Pharmaceuticals)
222 Northern, Northern
BHD85000 Annually
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Our client, a leader in pharmaceutical innovation, is seeking a highly accomplished Senior Research Scientist to join their dedicated R&D team in Shakhura, Northern, BH . This crucial role involves conducting cutting-edge research, developing novel drug candidates, and contributing significantly to the advancement of new therapeutic solutions. You will be responsible for designing and executing complex experimental protocols, analyzing scientific data, interpreting results, and preparing comprehensive reports and publications. Key responsibilities include leading specific research projects, collaborating with cross-functional teams comprising chemists, biologists, and pharmacologists, and staying abreast of the latest scientific literature and technological advancements in the field. The ideal candidate will possess a PhD in a relevant scientific discipline (e.g., Pharmacology, Biochemistry, Molecular Biology, Medicinal Chemistry) and a strong background in drug discovery and development. Proven experience in experimental design, data analysis using statistical software, and a strong publication record are essential. You should have expertise in relevant laboratory techniques and instrumentation. We are looking for a passionate, detail-oriented scientist with excellent problem-solving abilities and a commitment to scientific rigor. This is an exceptional opportunity to work in a state-of-the-art facility, contribute to impactful research, and advance your career in the pharmaceutical industry. We offer a stimulating research environment and a competitive compensation package. If you are driven by scientific curiosity and eager to make a difference in patient lives, we invite you to apply.
Key Responsibilities:
Key Responsibilities:
- Design and execute complex experiments to identify and validate new drug targets.
- Develop and optimize novel assays and methodologies for drug discovery.
- Conduct in-depth analysis of experimental data, utilizing statistical tools and software.
- Interpret results and prepare comprehensive reports, presentations, and scientific publications.
- Lead specific research projects, manage timelines, and coordinate with team members.
- Collaborate effectively with internal and external stakeholders, including cross-functional teams.
- Stay current with scientific literature, emerging technologies, and industry trends.
- Maintain laboratory equipment and ensure compliance with safety protocols.
- Contribute to the development of intellectual property and patent applications.
- Mentor junior researchers and contribute to knowledge sharing within the team.
- PhD in Pharmacology, Biochemistry, Molecular Biology, Medicinal Chemistry, or a related life science field.
- Minimum of 5-7 years of post-doctoral or industry research experience in drug discovery.
- Demonstrated expertise in experimental design, execution, and data analysis.
- Proficiency in relevant laboratory techniques and instrumentation (e.g., cell culture, molecular biology techniques, high-throughput screening).
- Strong understanding of pharmacology, physiology, and disease mechanisms.
- Excellent written and verbal communication skills, with a proven publication record.
- Ability to work independently and as part of a collaborative team.
- Strong analytical and problem-solving skills.
- Familiarity with data analysis software (e.g., GraphPad Prism, R).
- Experience in a specific therapeutic area is a plus.
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4
Senior Formulation Scientist - Pharmaceuticals
00405 Hamad Town, Northern
BHD90000 Annually
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Our client, a prominent pharmaceutical company, is seeking a highly skilled Senior Formulation Scientist to join their Research & Development department in Hamad Town, Northern, BH . This role is critical in developing innovative and effective pharmaceutical formulations for a range of therapeutic areas. The ideal candidate will possess extensive experience in formulation development, a deep understanding of drug delivery systems, and a commitment to scientific rigor.
Responsibilities:
Qualifications:
Responsibilities:
- Design, develop, and optimize pharmaceutical formulations for various dosage forms (e.g., oral solids, liquids, injectables, topical).
- Conduct pre-formulation studies to characterize drug substances and excipients.
- Perform compatibility studies between drug products and packaging materials.
- Develop and validate analytical methods for formulation testing and quality control.
- Prepare and review formulation development reports, regulatory documentation, and batch records.
- Troubleshoot formulation challenges and implement effective solutions.
- Stay abreast of the latest advancements in drug delivery technologies, formulation science, and regulatory guidelines.
- Collaborate with analytical development, process development, and regulatory affairs teams to ensure successful product development and registration.
- Manage formulation development projects, ensuring timely completion and adherence to project timelines and budgets.
- Conduct stability studies according to ICH guidelines and interpret results.
- Scale-up formulations from laboratory to pilot and commercial manufacturing scales.
- Evaluate and select appropriate excipients for formulation development.
- Supervise and mentor junior formulation scientists and technicians.
- Ensure all laboratory activities comply with Good Manufacturing Practices (GMP) and safety regulations.
- Contribute to the development of intellectual property through innovative formulation approaches.
- Participate in scientific meetings and conferences, presenting research findings.
- Review scientific literature to identify new formulation strategies and technologies.
- Ensure the quality and integrity of all research data.
- Support the transfer of developed formulations to manufacturing.
- Assist in the preparation of Investigational New Drug (IND) and New Drug Application (NDA) submissions.
Qualifications:
- Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, or a related field.
- Minimum of 5 years of experience in pharmaceutical formulation development.
- In-depth knowledge of various dosage forms and drug delivery systems.
- Experience with formulation development techniques and analytical instrumentation (e.g., HPLC, dissolution testing, particle size analysis).
- Understanding of GMP regulations and ICH guidelines.
- Strong scientific and problem-solving skills.
- Excellent written and verbal communication skills, with experience in technical writing.
- Proven ability to manage projects and work effectively in a team environment.
- Experience with scale-up and technology transfer is a plus.
- Familiarity with solid dosage form manufacturing processes (e.g., granulation, tableting, coating) is advantageous.
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5
Senior Formulation Scientist (Pharmaceuticals)
10221 Seef, Capital
BHD115000 Annually
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Our client seeks a dedicated Senior Formulation Scientist to join their innovative pharmaceutical development team in Seef, Capital, BH . This role is central to the design, development, and optimization of stable, effective, and patient-friendly dosage forms for novel drug candidates. You will lead projects focused on pre-formulation studies, excipient selection, formulation development, and scale-up activities for various dosage forms, including oral solid dosage, injectables, and topical preparations. Responsibilities include conducting compatibility studies, developing analytical methods for drug product characterization, and performing stability testing under various conditions. You will also be responsible for troubleshooting formulation challenges, preparing documentation for regulatory submissions, and collaborating with manufacturing and quality assurance departments.
The successful candidate will possess a PhD or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, or a related discipline, with a minimum of 6 years of hands-on experience in pharmaceutical formulation development. Demonstrated expertise in solid-state characterization techniques (e.g., XRD, DSC, TGA), dissolution testing, and pharmacokinetic profiling is essential. Experience with various dosage forms and delivery systems, including controlled-release technologies, is highly preferred. Strong understanding of regulatory guidelines (e.g., FDA, EMA) pertaining to drug product development and a proven ability to manage multiple projects simultaneously are required. Excellent analytical, problem-solving, and communication skills are necessary. The ability to work independently and as part of a team, contributing to a fast-paced R&D environment, is crucial. This position offers a chance to contribute to bringing life-changing medicines to patients.
The successful candidate will possess a PhD or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemical Engineering, or a related discipline, with a minimum of 6 years of hands-on experience in pharmaceutical formulation development. Demonstrated expertise in solid-state characterization techniques (e.g., XRD, DSC, TGA), dissolution testing, and pharmacokinetic profiling is essential. Experience with various dosage forms and delivery systems, including controlled-release technologies, is highly preferred. Strong understanding of regulatory guidelines (e.g., FDA, EMA) pertaining to drug product development and a proven ability to manage multiple projects simultaneously are required. Excellent analytical, problem-solving, and communication skills are necessary. The ability to work independently and as part of a team, contributing to a fast-paced R&D environment, is crucial. This position offers a chance to contribute to bringing life-changing medicines to patients.
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6
Clinical Research Associate (Pharmaceuticals)
942 Seef, Capital
BHD70000 Annually
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Posted 2 days ago
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Our client, a leading pharmaceutical company, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to support their innovative drug development programs. This is a full-time position located in Jidhafs, Capital, BH , focused on ensuring the quality and integrity of clinical trials. You will be responsible for monitoring clinical trial sites to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. This involves conducting site visits, reviewing essential documents, and verifying data accuracy and completeness.
Key responsibilities include screening, selecting, and training potential investigators and site staff. You will manage communication between study sites and the sponsor, resolve data queries, and ensure timely reporting of adverse events. Site management activities will include oversight of study supplies, maintenance of regulatory binders, and ensuring patient safety and rights are protected throughout the trial. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field, with at least 3 years of experience as a CRA or in a similar clinical research role within the pharmaceutical or biotechnology industry. Strong knowledge of ICH-GCP guidelines, clinical trial processes, and regulatory requirements is essential. Excellent organizational, communication, and interpersonal skills are mandatory, as is the ability to work independently and manage multiple tasks effectively. Familiarity with Electronic Data Capture (EDC) systems and medical terminology is required. A proactive approach to problem-solving and a commitment to maintaining high-quality standards in clinical research are crucial. This role offers a compelling opportunity to contribute to life-saving medical advancements and advance your career in clinical research within a supportive and innovative environment.
Key responsibilities include screening, selecting, and training potential investigators and site staff. You will manage communication between study sites and the sponsor, resolve data queries, and ensure timely reporting of adverse events. Site management activities will include oversight of study supplies, maintenance of regulatory binders, and ensuring patient safety and rights are protected throughout the trial. The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field, with at least 3 years of experience as a CRA or in a similar clinical research role within the pharmaceutical or biotechnology industry. Strong knowledge of ICH-GCP guidelines, clinical trial processes, and regulatory requirements is essential. Excellent organizational, communication, and interpersonal skills are mandatory, as is the ability to work independently and manage multiple tasks effectively. Familiarity with Electronic Data Capture (EDC) systems and medical terminology is required. A proactive approach to problem-solving and a commitment to maintaining high-quality standards in clinical research are crucial. This role offers a compelling opportunity to contribute to life-saving medical advancements and advance your career in clinical research within a supportive and innovative environment.
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7
Clinical Research Associate - Pharmaceuticals
10001 Tubli, Central
BHD70000 Annually
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Posted 4 days ago
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Our client, a leading pharmaceutical company dedicated to advancing global health, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their remote clinical operations team. This position will be based remotely, allowing you to contribute to vital drug development programs from anywhere. The CRA plays a crucial role in ensuring the quality, integrity, and compliance of clinical trials by monitoring study sites, verifying data, and adhering to Good Clinical Practice (GCP) guidelines. You will be the primary point of contact for clinical trial sites, supporting investigators and site staff to ensure accurate and timely execution of study protocols. This role demands strong organizational skills, attention to detail, and a solid understanding of the clinical trial process.
Key Responsibilities:
Key Responsibilities:
- Conduct site initiation visits, routine monitoring visits, and close-out visits according to study-specific plans and regulatory requirements.
- Verify the accuracy, completeness, and integrity of clinical trial data through source data verification (SDV).
- Ensure compliance with study protocols, SOPs, GCP guidelines, and all applicable regulatory requirements.
- Build and maintain strong working relationships with clinical investigators and site staff.
- Train site personnel on study-specific procedures and regulatory requirements.
- Oversee site regulatory compliance, including essential document collection and maintenance.
- Monitor patient safety and report adverse events (AEs) and serious adverse events (SAEs) promptly.
- Manage site issues and escalate them to the Clinical Trial Manager (CTM) as necessary.
- Prepare monitoring visit reports and follow-up on action items with study sites.
- Contribute to the development of study protocols, informed consent forms, and other study documents.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific field.
- Minimum of 3 years of experience as a Clinical Research Associate (CRA) or in a similar clinical trial monitoring role.
- In-depth knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trials.
- Experience in monitoring studies across various therapeutic areas.
- Strong understanding of clinical trial processes and documentation.
- Excellent written and verbal communication skills.
- Proficiency in using electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to travel to sites as needed (if applicable, though primarily remote).
- Strong organizational skills and meticulous attention to detail.
- Ability to work independently and effectively manage time and priorities in a remote setting.
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8
Clinical Research Associate - Pharmaceuticals
407 Busaiteen, Muharraq
BHD40000 Annually
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Posted 4 days ago
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Job Description
Our client, a prominent pharmaceutical company dedicated to advancing healthcare, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in **Busaiteen, Muharraq, BH**. This critical role involves overseeing and managing clinical trial activities to ensure compliance with protocols, regulations, and quality standards. The ideal candidate will have a strong background in clinical research, excellent understanding of GCP (Good Clinical Practice) guidelines, and a passion for contributing to the development of life-saving medicines. You will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring data accuracy and integrity. This position requires strong analytical skills, attention to detail, and the ability to build rapport with investigators and site staff. Travel to clinical trial sites will be required. The successful applicant will possess a Bachelor's degree in a life science or related field and have at least 2-3 years of experience as a CRA. Excellent written and verbal communication skills are essential, along with proficiency in clinical trial management software. This is an excellent opportunity for a dedicated professional to advance their career in a supportive and innovative environment, making a significant impact on patient health.
Key Responsibilities:
Key Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocol and regulatory requirements.
- Verify accuracy and completeness of clinical data.
- Initiate, monitor, and close-out clinical trial sites.
- Conduct site visits, including qualification, initiation, routine monitoring, and close-out.
- Ensure adherence to Good Clinical Practice (GCP) guidelines.
- Train and support site personnel on study procedures.
- Manage and maintain study documentation and essential records.
- Communicate effectively with investigators, site staff, and study sponsors.
- Identify and report adverse events and deviations.
- Prepare site monitoring reports and ensure timely submission.
- Participate in study team meetings and contribute to study progress.
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