What Jobs are available for Medical Affairs in Bahrain?
Showing 556 Medical Affairs jobs in Bahrain
Medical Affairs Manager
808 Saar, Northern
BHD110000 Annually
WhatJobs Direct
Posted 1 day ago
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Job Description
Our client is seeking a highly qualified and experienced Medical Affairs Manager to join their fully remote pharmaceutical team. This critical role will focus on developing and executing medical strategies to support the company's product portfolio and therapeutic areas. You will serve as a key scientific and medical expert, engaging with healthcare professionals, key opinion leaders (KOLs), and internal teams to disseminate scientific information and gather insights. The ideal candidate will possess a strong scientific background, a deep understanding of pharmaceutical drug development, and a proven track record in medical affairs or a related field. Your responsibilities will include developing medical education materials, planning and executing scientific exchange activities, and contributing to the development of clinical trial protocols and publications. This position requires excellent communication, leadership, and strategic thinking skills, along with the ability to work independently and collaborate effectively in a remote environment. You will play a pivotal role in ensuring that the company's medical strategies are aligned with both scientific advancements and market needs. A commitment to ethical conduct and regulatory compliance is paramount. This is an outstanding opportunity to influence medical strategy and contribute to significant advancements in patient care within a dynamic and innovative pharmaceutical company, all from the convenience of your home office. Key responsibilities include:
- Developing and implementing comprehensive medical affairs strategies.
- Serving as a scientific and medical expert for assigned products/therapeutic areas.
- Engaging with Key Opinion Leaders (KOLs) and healthcare professionals (HCPs) to foster scientific exchange.
- Developing medical education materials and training programs.
- Contributing to the planning and execution of scientific advisory boards and symposia.
- Providing medical input for clinical trial design, data interpretation, and publications.
- Reviewing and approving promotional and non-promotional materials for medical accuracy.
- Analyzing medical literature and competitive intelligence to inform strategy.
- Collaborating with R&D, marketing, and regulatory affairs teams.
- Ensuring compliance with all relevant industry regulations and ethical guidelines.
- Managing medical affairs budget and resources effectively.
- Advanced degree (MD, PharmD, PhD) in a relevant scientific or medical discipline.
- Minimum of 5 years of experience in pharmaceutical medical affairs or a closely related field.
- Strong understanding of drug development, clinical trials, and regulatory affairs.
- Excellent scientific communication and presentation skills.
- Proven ability to engage effectively with Key Opinion Leaders (KOLs).
- Strong strategic thinking and analytical capabilities.
- Demonstrated leadership and project management skills.
- Proficiency in working with digital collaboration tools in a remote setting.
- Ability to travel occasionally as required.
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0
Senior Medical Affairs Manager
100 Busaiteen, Muharraq
BHD140000 Annually
WhatJobs Direct
Posted 4 days ago
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Job Description
Our client, a prominent pharmaceutical company, is seeking an experienced Senior Medical Affairs Manager to join their dynamic team in Busaiteen, Muharraq, BH . This role operates on a hybrid model, blending strategic office-based work with remote flexibility. The Senior Medical Affairs Manager will play a crucial role in developing and executing medical affairs strategies, ensuring accurate and compliant scientific communication. You will be responsible for engaging with key opinion leaders (KOLs), managing medical information requests, and supporting the clinical development and lifecycle management of assigned products. The ideal candidate will possess a strong scientific background, excellent communication skills, and a deep understanding of the pharmaceutical industry and regulatory landscape. Key responsibilities include developing scientific exchange plans, overseeing the publication strategy, and providing medical expertise to cross-functional teams, including marketing, R&D, and regulatory affairs. You will serve as a trusted scientific resource for internal and external stakeholders. The ability to analyze complex scientific data, translate it into clear messaging, and develop compelling scientific materials is essential. This position requires strong leadership capabilities and the ability to manage multiple projects simultaneously. We are looking for a proactive individual who can contribute to the strategic direction of medical affairs, driving evidence-based communication and enhancing the medical value of our client's portfolio. Collaboration and the ability to build consensus among diverse stakeholders are key. This role offers a significant opportunity to influence medical strategy and contribute to advancing patient care through scientifically sound information. Your expertise will be vital in shaping medical perceptions and ensuring the appropriate use of our client's innovative therapies.
Key Responsibilities:
Key Responsibilities:
- Develop and implement comprehensive medical affairs strategies.
- Engage with and build relationships with Key Opinion Leaders (KOLs) in relevant therapeutic areas.
- Oversee the development and execution of publication plans.
- Manage medical information requests and ensure timely, accurate responses.
- Provide medical and scientific expertise to cross-functional teams.
- Support clinical trial activities and lifecycle management of assigned products.
- Ensure all medical affairs activities are conducted in compliance with regulatory guidelines.
- Analyze scientific data and develop evidence-based communication materials.
- Contribute to strategic planning for product launches and post-launch activities.
- Evaluate scientific literature and identify key research opportunities.
- Advanced degree (MD, PharmD, PhD) in a life science or medical field.
- Minimum of 7 years of experience in medical affairs or a related role within the pharmaceutical industry.
- Proven experience in engaging with KOLs and managing scientific communications.
- Strong understanding of clinical development, pharmacology, and regulatory affairs.
- Excellent written and verbal communication skills, with the ability to present complex scientific information.
- Demonstrated leadership and project management abilities.
- Experience in (Specify Therapeutic Area, e.g., Oncology, Cardiology) is highly desirable.
- Ability to work effectively in a hybrid work environment.
- Proficiency in medical terminology and scientific writing.
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1
Principal Medical Affairs Director
706 Al Jasra
BHD150000 Annually
WhatJobs Direct
Posted 1 day ago
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Job Description
Our client, a leading global pharmaceutical company at the forefront of medical innovation, is seeking an exceptional Principal Medical Affairs Director to join their distinguished and fully remote team. This critical role will shape the strategic direction of medical affairs activities, driving evidence generation and dissemination for key therapeutic areas. You will be instrumental in establishing and maintaining strong relationships with key opinion leaders (KOLs), medical societies, and patient advocacy groups, ensuring robust scientific exchange and supporting the clinical development and lifecycle management of our groundbreaking therapies.
Responsibilities:
Responsibilities:
- Develop and execute the global medical affairs strategy for assigned products, aligned with global R&D and commercial objectives.
- Lead the planning and execution of medical communication strategies, including publications, presentations at scientific congresses, and development of medical information materials.
- Engage with Key Opinion Leaders (KOLs), investigators, and scientific experts to foster collaborative relationships and gather insights.
- Oversee the design, implementation, and completion of Phase IV clinical studies, post-marketing research, and investigator-initiated studies (IIS).
- Provide medical and scientific expertise to internal cross-functional teams, including R&D, clinical development, regulatory affairs, and marketing.
- Ensure compliance with all relevant industry regulations, ethical guidelines, and company policies.
- Train and mentor medical science liaisons (MSLs) and other medical affairs personnel.
- Review and approve promotional and non-promotional materials to ensure scientific accuracy and regulatory compliance.
- Contribute to the development of disease state education initiatives.
- Effectively communicate scientific data and strategic plans within a remote work environment.
- Doctoral degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or medical discipline.
- Minimum of 10 years of experience in the pharmaceutical industry, with a significant portion in Medical Affairs.
- Proven track record in developing and implementing successful medical affairs strategies.
- Deep understanding of clinical trial design, execution, and data analysis.
- Extensive experience in engaging with KOLs and medical societies.
- Excellent knowledge of regulatory requirements and ethical guidelines governing pharmaceutical promotion and medical affairs.
- Exceptional scientific communication, presentation, and writing skills.
- Demonstrated ability to lead and influence within a matrix organization and in a remote setting.
- Strong strategic thinking and problem-solving capabilities.
- Proficiency in managing budgets and cross-functional projects.
- Ability to work independently and proactively manage a remote workload.
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2
Principal Medical Affairs Manager
55503 Zallaq, Southern
BHD130000 Annually
WhatJobs Direct
Posted 1 day ago
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Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly accomplished and strategic Principal Medical Affairs Manager to join their expanding team in a fully remote capacity. This pivotal role will drive medical strategy, foster key opinion leader (KOL) engagement, and ensure the scientific integrity of our therapeutic products. The successful candidate will play a crucial part in translating complex scientific data into clear, impactful medical communications and supporting the life cycle management of our pharmaceutical portfolio.
Key Responsibilities:
The ideal candidate will hold an advanced degree (MD, PharmD, PhD) in a relevant scientific or medical discipline, with a minimum of 10 years of progressive experience in medical affairs within the pharmaceutical or biotechnology industry. A deep understanding of regulatory requirements, clinical trial design, and pharmacovigilance is essential. Demonstrated experience in KOL engagement, scientific communication, and strategic planning is critical. Exceptional leadership, analytical, and presentation skills are required to succeed in this remote leadership role. A proven track record of successfully launching and supporting pharmaceutical products is highly desirable. This is a unique opportunity to shape medical strategy and contribute to advancing patient care through innovative therapies.
Key Responsibilities:
- Develop and execute comprehensive medical affairs strategies aligned with corporate objectives and therapeutic area goals.
- Identify, engage, and cultivate relationships with key opinion leaders (KOLs) and scientific experts globally.
- Oversee the planning and execution of medical education programs, symposia, and advisory boards.
- Review and approve promotional and non-promotional materials to ensure scientific accuracy and compliance with regulatory guidelines.
- Contribute to the development of clinical trial protocols and data interpretation for assigned products.
- Serve as a scientific expert and resource for internal teams, including marketing, sales, and R&D.
- Prepare and deliver scientific presentations at national and international medical conferences.
- Analyze market trends, competitor activities, and emerging scientific literature to inform strategy.
- Manage medical affairs budgets and vendor relationships effectively.
- Mentor and develop junior members of the medical affairs team.
The ideal candidate will hold an advanced degree (MD, PharmD, PhD) in a relevant scientific or medical discipline, with a minimum of 10 years of progressive experience in medical affairs within the pharmaceutical or biotechnology industry. A deep understanding of regulatory requirements, clinical trial design, and pharmacovigilance is essential. Demonstrated experience in KOL engagement, scientific communication, and strategic planning is critical. Exceptional leadership, analytical, and presentation skills are required to succeed in this remote leadership role. A proven track record of successfully launching and supporting pharmaceutical products is highly desirable. This is a unique opportunity to shape medical strategy and contribute to advancing patient care through innovative therapies.
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3
Principal Medical Affairs Specialist
602 Tubli
BHD95000 Annually
WhatJobs Direct
Posted 1 day ago
Job Viewed
Job Description
Our client, a renowned pharmaceutical company, is seeking a highly experienced Principal Medical Affairs Specialist for a fully remote position. This senior role is instrumental in developing and executing strategic medical affairs plans that support the lifecycle management of key pharmaceutical products. You will serve as a scientific and clinical expert, engaging with Key Opinion Leaders (KOLs), investigators, and healthcare professionals to foster collaborations and disseminate scientific information. Your responsibilities will include developing high-quality medical education materials, reviewing promotional and non-promotional content for scientific accuracy, and contributing to the planning and execution of medical advisory boards and scientific congresses. You will also play a crucial role in identifying research gaps and opportunities, and contributing to the development of clinical trial protocols and study designs. A deep understanding of therapeutic areas, regulatory guidelines, and ethical principles governing medical affairs is essential. The ideal candidate will possess exceptional scientific acumen, strong communication and presentation skills, and the ability to influence and build consensus among diverse stakeholders. Proven experience in medical affairs, clinical research, or a related scientific role within the pharmaceutical industry is required. This is an exceptional opportunity for a dedicated professional to drive impactful medical strategies remotely.
Responsibilities:
Responsibilities:
- Develop and implement comprehensive medical affairs strategies for assigned products.
- Engage with Key Opinion Leaders (KOLs) and healthcare professionals to build relationships and gather insights.
- Review and approve medical and marketing materials for scientific accuracy and compliance.
- Contribute to the planning and execution of medical advisory boards and scientific symposia.
- Identify and disseminate scientific and clinical data relevant to therapeutic areas.
- Support the design and implementation of investigator-initiated studies.
- Provide scientific and clinical expertise to internal teams, including marketing and R&D.
- Ensure all medical affairs activities are conducted in accordance with regulatory guidelines and ethical standards.
- Contribute to the development of medical communication plans.
- Stay abreast of clinical research advancements and competitive intelligence.
- Advanced degree (Pharm.D., Ph.D., M.D.) in a life science or healthcare-related field.
- Minimum of 8 years of progressive experience in medical affairs, clinical development, or medical science liaison roles within the pharmaceutical industry.
- Deep understanding of a specific therapeutic area(s) and clinical trial methodology.
- Proven experience in engaging with KOLs and healthcare professionals.
- Excellent written, verbal, and presentation communication skills.
- Strong understanding of pharmaceutical regulations and compliance requirements.
- Ability to think strategically and translate scientific data into actionable plans.
- Demonstrated ability to work independently and collaboratively in a remote team environment.
- Experience in developing medical education content and reviewing promotional materials.
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4
Senior Medical Affairs Manager - Pharmaceutical
11223 Manama, Capital
BHD140000 Annually
WhatJobs Direct
Posted 4 days ago
Job Viewed
Job Description
Our client, a global pharmaceutical powerhouse, is seeking a highly experienced Senior Medical Affairs Manager to lead their medical strategy and execution for key therapeutic areas. This is a fully remote position, enabling you to contribute to vital healthcare initiatives from any location. You will be responsible for developing and implementing comprehensive medical affairs plans, engaging with key opinion leaders (KOLs), supporting clinical research, and ensuring the dissemination of accurate scientific information. The ideal candidate will possess a strong medical or scientific background, extensive experience in the pharmaceutical industry, and exceptional communication and leadership skills.
Key Responsibilities:
Key Responsibilities:
- Develop and execute strategic medical affairs plans in alignment with company objectives and therapeutic area priorities.
- Engage with Key Opinion Leaders (KOLs), investigators, and healthcare professionals to foster scientific exchange and collaboration.
- Provide scientific and medical expertise to internal teams, including marketing, R&D, and regulatory affairs.
- Support the design and execution of clinical research studies, including investigator-initiated trials (IITs).
- Review and approve promotional and non-promotional materials to ensure scientific accuracy and compliance.
- Stay abreast of the latest scientific advancements, clinical data, and regulatory landscapes in assigned therapeutic areas.
- Contribute to the development of medical education programs and scientific communications.
- Represent the company at scientific congresses and medical meetings.
- Manage the medical affairs budget effectively.
- Mentor and guide junior medical affairs professionals.
- Advanced degree (MD, PharmD, PhD, or equivalent) in a life sciences or medical field.
- Minimum of 7 years of progressive experience in medical affairs within the pharmaceutical or biotechnology industry.
- Proven track record of developing and implementing successful medical affairs strategies.
- Deep understanding of clinical trial design, data analysis, and medical writing.
- Experience in engaging and managing relationships with Key Opinion Leaders (KOLs).
- In-depth knowledge of pharmaceutical regulations, compliance guidelines, and ethical standards.
- Excellent written and verbal communication, presentation, and interpersonal skills.
- Strong analytical and problem-solving abilities.
- Ability to work independently, manage complex projects, and collaborate effectively in a remote team environment.
- Experience in specific therapeutic areas is a significant advantage.
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5
Principal Medical Affairs Manager - Remote
10221 Riffa, Southern
BHD150000 Annually
WhatJobs Direct
Posted 1 day ago
Job Viewed
Job Description
Our client, a world-leading pharmaceutical company, is seeking an experienced and strategic Principal Medical Affairs Manager to join their innovative team. This is a pivotal, fully remote role focused on driving medical strategy and engagement within key therapeutic areas. You will be at the forefront of scientific communication, expert engagement, and the dissemination of clinical data, playing a crucial role in shaping the company's medical narrative. Your responsibilities will include developing and executing comprehensive medical affairs plans, managing key opinion leader (KOL) relationships, and ensuring the scientific accuracy and compliance of all medical communications. You will also lead the planning and execution of medical education programs, advisory boards, and scientific congress activities. Collaboration with cross-functional teams, including R&D, clinical operations, marketing, and regulatory affairs, will be essential. The ideal candidate will possess an advanced degree (MD, PharmD, PhD) in a relevant life science discipline, coupled with significant experience (8+ years) in medical affairs within the pharmaceutical or biotechnology industry. Demonstrated success in developing and implementing medical strategies, a deep understanding of the drug development lifecycle, and a strong scientific background in relevant therapeutic areas are required. Exceptional communication, presentation, and interpersonal skills are paramount, as is the ability to engage effectively with the scientific and medical community. Proven leadership capabilities and the ability to work autonomously in a remote setting are essential. This role supports strategic initiatives relevant to Riffa, Southern, BH , but is performed entirely remotely, offering global reach and flexibility. Our client is committed to scientific excellence and innovation, providing a stimulating and rewarding environment for professionals passionate about advancing patient care through cutting-edge pharmaceutical solutions.
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6
Clinical Research Associate
2217 Seef, Capital
BHD80000 Annually
WhatJobs Direct
Posted today
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Job Description
Our client, a leading pharmaceutical research organization, is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their expanding team. This role involves significant fieldwork and requires a professional who can balance remote work with site visits to ensure the smooth execution of clinical trials. You will be responsible for monitoring investigational sites to verify compliance with protocols, regulations, and Good Clinical Practice (GCP) guidelines. This includes ensuring the accuracy, completeness, and quality of data recorded in case report forms (CRFs) and other study documents. The CRA will act as the primary liaison between the sponsor and the investigational sites, fostering strong working relationships with investigators and site staff. Key responsibilities include site initiation visits, routine monitoring visits, and site closure visits. You will also be tasked with identifying and resolving site-specific issues, training site personnel on study procedures, and ensuring adherence to safety reporting requirements. The ideal candidate will possess a strong understanding of drug development processes, regulatory requirements (FDA, EMA, etc.), and clinical trial management systems. A Bachelor's degree in a life science, nursing, or related field is required; an advanced degree is a plus. Proven experience as a CRA, with a demonstrated ability to manage multiple studies and sites simultaneously, is essential. Excellent organizational, time management, and communication skills are critical for success in this role. You must be proficient in using clinical trial software and electronic data capture (EDC) systems. The ability to travel to investigational sites in and around **Seef, Capital, BH**, and potentially other locations as needed, is a core requirement of this hybrid position. This role offers the opportunity to contribute to groundbreaking pharmaceutical research and development, working on innovative therapies that have the potential to improve patient lives. We are looking for a proactive, detail-oriented professional who is passionate about clinical research and committed to maintaining the highest standards of scientific integrity and ethical conduct.
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7
Clinical Research Associate
21200 Manama, Capital
BHD90000 Annually
WhatJobs Direct
Posted 2 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join their dynamic clinical operations team. This role is based in Manama and involves on-site responsibilities at various clinical trial sites. As a CRA, you will be responsible for monitoring clinical trials to ensure data integrity, patient safety, and adherence to study protocols and regulatory guidelines. Your primary focus will be on site management, including site initiation visits, routine monitoring visits, and close-out visits. You will liaise between investigators, site staff, and the sponsor, ensuring effective communication and problem resolution.
Key responsibilities include verifying source data, reviewing case report forms (CRFs), managing essential regulatory documents, and ensuring compliance with Good Clinical Practice (GCP) and all applicable regulations. You will also be involved in subject recruitment, informed consent process oversight, and drug accountability. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory requirements (e.g., FDA, EMA), and medical terminology. Excellent organizational, analytical, and interpersonal skills are essential, as is the ability to travel to various trial sites as required. A Bachelor's degree in a life science, nursing, or related field is typically required, along with previous experience as a CRA or in a clinical research support role. This is an excellent opportunity for a motivated professional to contribute to the development of innovative pharmaceutical products and advance patient care. We offer a competitive salary and benefits package.
Location: Manama, Capital, BH
Key responsibilities include verifying source data, reviewing case report forms (CRFs), managing essential regulatory documents, and ensuring compliance with Good Clinical Practice (GCP) and all applicable regulations. You will also be involved in subject recruitment, informed consent process oversight, and drug accountability. The ideal candidate will possess a strong understanding of clinical trial processes, regulatory requirements (e.g., FDA, EMA), and medical terminology. Excellent organizational, analytical, and interpersonal skills are essential, as is the ability to travel to various trial sites as required. A Bachelor's degree in a life science, nursing, or related field is typically required, along with previous experience as a CRA or in a clinical research support role. This is an excellent opportunity for a motivated professional to contribute to the development of innovative pharmaceutical products and advance patient care. We offer a competitive salary and benefits package.
Location: Manama, Capital, BH
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8
Clinical Research Scientist
20121 Hamad Town, Northern
BHD95000 Annually
WhatJobs Direct
Posted 3 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is looking for a dedicated and skilled Clinical Research Scientist to join their dynamic team. This role is integral to the planning, execution, and analysis of clinical trials, contributing to the development of innovative new medicines. The successful candidate will be responsible for designing study protocols, managing data collection and analysis, ensuring adherence to regulatory guidelines, and preparing scientific reports. Key duties include collaborating with investigators and site staff, monitoring trial progress, interpreting clinical data, and contributing to the publication of research findings. The ideal candidate will possess a strong scientific background in a relevant therapeutic area, extensive knowledge of Good Clinical Practice (GCP) and regulatory requirements (FDA, EMA), and excellent analytical and statistical skills. A PhD or Master's degree in a life science field is typically required. This position is based in our client's state-of-the-art facility and requires regular on-site presence to effectively manage and oversee clinical research activities in the **Hamad Town, Northern, BH** area. We seek a highly motivated individual with a passion for advancing medical science and a commitment to patient safety. The ability to work effectively in a team, manage multiple projects, and communicate complex scientific information clearly is essential. This role offers an exceptional opportunity to be at the forefront of pharmaceutical innovation, working with cutting-edge research and contributing to life-changing therapies. Continuous learning and professional development are encouraged, ensuring you remain at the pinnacle of your field. Your expertise will directly impact the success of critical drug development programs, making a tangible difference in healthcare.
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