What Jobs are available for Medical Communications in Bahrain?

• 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.

• 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.

• 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.

• Develop and implement comprehensive medical affairs strategies for assigned therapeutic areas.
• Serve as a scientific expert and engage with KOLs to foster productive scientific exchange.
• Oversee the development and execution of publication plans in line with scientific strategies.
• Manage the creation and review of scientific and educational materials for accuracy and compliance.
• Collaborate with R&D, Clinical Development, Marketing, and Regulatory Affairs to ensure alignment of medical strategy with overall business objectives.
• Support the planning and execution of medical advisory boards and scientific meetings.
• Ensure all medical affairs activities comply with industry regulations, ethical standards, and company policies.
• Contribute to the strategic planning and execution of clinical research and real-world evidence generation.
• Mentor and develop junior members of the medical affairs team.
• Stay abreast of the latest scientific advancements, clinical data, and competitive landscape within therapeutic areas.

• Advanced scientific degree (MD, PhD, PharmD, or equivalent) in a relevant scientific or medical discipline.
• Minimum of 10 years of progressive experience in medical affairs, clinical research, or a related field within the pharmaceutical or biotechnology industry.
• Proven track record of developing and executing successful medical affairs strategies.
• Extensive experience engaging with KOLs and managing scientific communication.
• Deep understanding of clinical research methodologies, data analysis, and regulatory requirements.
• Exceptional scientific writing and presentation skills.
• Strong leadership, strategic thinking, and project management capabilities.
• Ability to work independently and effectively in a remote, cross-functional environment.
• Experience with therapeutic areas relevant to our client's portfolio.
• Commitment to ethical conduct and compliance.

• Develop and implement comprehensive medical affairs strategies for assigned oncology products.
• Identify, engage, and build strong relationships with key opinion leaders (KOLs) and external experts in oncology.
• Serve as a scientific and clinical expert for assigned therapeutic areas, responding to medical inquiries from healthcare professionals.
• Develop and review scientific and medical communication materials, including publications, presentations, and educational content.
• Provide medical input for clinical trial design, execution, and data interpretation.
• Support the planning and execution of advisory boards and scientific meetings.
• Ensure all medical affairs activities comply with relevant industry regulations, guidelines, and codes of conduct.
• Collaborate with cross-functional teams, including clinical development, regulatory affairs, marketing, and sales, to ensure alignment and successful execution of medical strategies.
• Contribute to the development of publication plans and review manuscripts for submission.
• Monitor the competitive landscape and emerging scientific data in oncology.
• Provide training and scientific support to internal teams as needed.
• Contribute to the strategic planning for lifecycle management of oncology products.

• M.D., Ph.D., Pharm.D., or other relevant advanced degree in a life science or medical field.
• Minimum of 7 years of experience in Medical Affairs, Clinical Development, or related roles within the pharmaceutical or biotechnology industry, with a strong focus on Oncology.
• In-depth knowledge of oncology therapeutics, disease states, and treatment paradigms.
• Proven experience in engaging with and managing relationships with Key Opinion Leaders (KOLs).
• Strong understanding of clinical trial methodology, data analysis, and interpretation.
• Excellent scientific communication and presentation skills.
• Thorough knowledge of industry regulations and compliance requirements (e.g., PhRMA Code, FDA guidelines).
• Demonstrated ability to think strategically and translate scientific data into actionable medical plans.
• Excellent interpersonal and collaboration skills, with the ability to work effectively in a remote, cross-functional team environment.
• Proficiency in scientific literature review and database searching.

Company Description

KPM - KEMET Precious Metal (KPM Group) began as a small retail shop in Suez City in 1935. Now in its fourth generation, this family-run business has developed a strong foundation of trust and integrity with its customers. Over the years, KPM expanded to Cairo and established Egypt's first gold factory. Today, the group boasts a full integration with a gold and diamond factory and covers 90% of jewelry retailers in the Egyptian market. Our brands include Bullion Trading Company BTC, GD&M, The Travel Boutique, Odyssey, Gemeva.

Role Overview:

The PR Consultant will be responsible for building, maintaining, and enhancing the brand's reputation in the luxury retail market. This role focuses on crafting a premium brand image that resonates with high-net-worth individuals, collectors, and luxury lifestyle audiences, while ensuring consistent visibility across traditional and digital media channels.

Qualifications

• Proven experience in luxury retail PR (preferably jewelry, high-end fashion, art, or antiques).
• Strong network of media, influencers, and industry contacts in luxury markets.
• Excellent written and verbal communication skills with a flair for luxury storytelling.
• Knowledge of high-net-worth consumer behavior and luxury market dynamics.
• Ability to organize high-profile events with attention to detail and exclusivity.
• Brand protection expertise.
• Fluent in English

Motivated and creative Public Relations Specialist seeking new opportunities to contribute my communication, media, and organizational skills within a professional and dynamic environment. I am passionate about building a positive image for organizations, managing media relations, and coordinating events that strengthen public engagement.

Key Skills:

• Strong written and verbal communication in Arabic and English.

• Experience in media coordination, social media management, and event planning.

• Ability to develop and execute PR strategies effectively.

• Excellent teamwork, creativity, and problem-solving abilities.

Goal:

Looking to join a reputable organization where I can grow professionally and add value through innovative communication and public relations strategies.