Medical Advisor
Overview
A Medical Advisor provides scientific and medical expertise to support product development, clinical trials, and regulatory compliance. They ensure drug efficacy, safety, and patient outcomes, guiding the design and execution of clinical studies. Collaborating with cross-functional teams, help align medical strategies with business objectives and engage with healthcare professionals, researchers, and regulatory bodies. The role also involves reviewing promotional materials for compliance and providing medical education to internal teams and healthcare providers.
A Medical Advisor provides scientific and medical expertise to support product development, clinical trials, and regulatory compliance. They ensure drug efficacy, safety, and patient outcomes, guiding the design and execution of clinical studies. Collaborating with cross-functional teams, help align medical strategies with business objectives and engage with healthcare professionals, researchers, and regulatory bodies. The role also involves reviewing promotional materials for compliance and providing medical education to internal teams and healthcare providers.
Start date: Candidate must begin working within a reasonable period.
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Role and Responsibilities
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EDUCATION:
Medical Degree (MD, MBBS, or equivalent). A Master’s degree or Doctorate in fields such as Pharmacology, Clinical Research, Medical Sciences, or Public Health is preferred. Additional certifications in clinical research or regulatory affairs are a plus.
Experience: 5 years of experience in the biopharmaceutical or healthcare industry, with a focus on medical affairs, clinical research, or pharmaceutical development.
SKILLS AND ABILITIES:
- Medical Expertise: Strong clinical knowledge across therapeutic areas and drug development.
- Regulatory Knowledge: Familiar with global and local drug approval processes and clinical trial regulations.
- Clinical Research: Experience in designing, monitoring, and interpreting clinical trials.
- Communication: Excellent verbal and written communication skills for cross-functional collaboration.
- Problem-Solving: Analytical ability to address challenges and make informed decisions.
- Collaboration: Ability to work well in cross-functional teams, including R&D, regulatory, and marketing.
- Strategic Thinking: Contribute to clinical development and business strategy.
- Time Management: Ability to manage multiple priorities and meet deadlines efficiently.
- Medical Writing: Skilled in preparing clinical documents, reports, and regulatory submissions.
- Ethical Judgment: Strong commitment to medical ethics and patient safety.
EQUAL OPPORTUNITY EMPLOYER: Dei Biopharma Ltd. provides equal opportunity and fair and equitable treatment in employment to all people without regard to race, color, religion, sex, national origin, age, disability, political affiliation, marital status, or sexual orientation.
How to Apply:
All interested candidates who meet the required qualifications and experience are invited to submit their CVs, Cover Letter & Academic documents (addressed to the Head Human Capital)
All Application documents should be merged as one document in PDF or .DOC / .DOCX, which should not exceed 10MB
Applications should be sent by email to recruitment@deibiopharma.com with the JOB TITLE IN THE SUBJECT LINE.
Should you not hear from us within fourteen (14) days from the closing date of this advertisement, you may consider your application to be unsuccessful.