Company Description DataClin is a Egypt-based Contract Research Organization (CRO) specializing in clinical data management, biostatistics, medical writing, clinical monitoring, pharmacovigilance, consultancy, medical affairs, and training services. The organization operates according to comprehensive international, regional, and local regulatory standards, while also respecting customer-specific requirements. With over 13 years in the market, DataClin has built a strong reputation as a reliable partner, collaborating with many of the top multinational pharmaceutical companies across diverse therapeutic areas. The team has extensive experience across all phases of clinical trials and post-marketing registries, covering the Middle East and Africa (MEA) region with tailored solutions that reflect local regulatory and cultural contexts. DataClin is committed to excellence, people development, and long-term partnerships grounded in professionalism, integrity, and consistent quality.
Role Description The Medical Affairs Manager will oversee medical affairs activities to support clinical research projects and pharmaceutical partners, ensuring scientific accuracy and alignment with regulatory and ethical standards. This full-time, on-site role based in Giza includes leading medical strategy, providing medical and scientific input into clinical trials, and collaborating closely with cross-functional teams such as clinical operations, pharmacovigilance, and biostatistics. The role involves reviewing and approving medical and promotional materials, supporting medical education initiatives, and maintaining up-to-date knowledge of relevant therapeutic areas and guidelines. The Medical Affairs Manager will engage with key stakeholders and subject matter experts, contribute to training programs, and help ensure that all medical affairs activities meet DataClin’s quality standards and partner expectations.
Qualifications
- * Candidates should possess strong Medical Affairs expertise, including experience in managing and aligning medical strategies with clinical and business objectives.
- Candidates should possess a solid background in Medicine, such as a medical degree or relevant clinical experience, and an understanding of therapeutic areas relevant to clinical research.
- Candidates should possess Regulatory Affairs knowledge, including familiarity with international, regional, and local regulatory requirements and guidelines in the MEA region.
- Candidates should possess experience or strong interest in Oncology or other key therapeutic areas, enabling effective scientific support for related clinical trials and projects.
- Candidates should possess Medical Education skills, including the ability to develop and deliver scientific training and educational materials for internal teams and external stakeholders.
- Candidates should have excellent written and verbal communication skills, strong analytical and critical thinking abilities, and a high level of professionalism and integrity.
- Relevant experience in a CRO or pharmaceutical environment, project management skills, and proficiency in English are highly beneficial; additional regional language skills are an advantage.
