Director, Medical Monitoring

• Serve as the primary medical contact for assigned clinical trials, ensuring protocol adherence and safety oversight.
• Address medical inquiries from investigators, regulatory agencies, and internal teams, ensuring consistent application of protocol guidelines.
• Monitor clinical trial conduct, assessing safety data, adverse events (AEs), serious adverse events (SAEs), and emerging safety signals.
• Provide medical expertise in study design, protocol development, and execution, collaborating with cross-functional teams to advance clinical programs.
• Support site selection, patient recruitment, and investigator engagement through regular interactions and guidance.
• Lead or co-lead clinical study teams, facilitating discussions and decision-making processes.
• Participate in interactions with regulatory authorities, preparing clinical documentation and supporting regulatory submissions.
• Collaborate with key opinion leaders (KOLs), clinical investigators, and external stakeholders to advance clinical development objectives.
• Develop and review essential study documents, including protocols, investigator brochures (IBs), informed consent forms (ICFs), data review plans, and clinical study reports (CSRs).
• Contribute to internal governance processes and strategic development discussions.
• Support publication planning and contribute to abstracts, posters, and manuscripts.

• Medical Degree (MD or equivalent) with a strong background in oncology and hematology.
• 10+ years of experience in pharmaceutical/biotech clinical development or relevant clinical research roles.
• At least 5 years of experience serving as a medical monitor for clinical trials.
• Extensive knowledge of clinical trial safety monitoring, adverse event assessment, and regulatory requirements.
• Familiarity with global regulatory frameworks, including FDA and EMA guidelines.
• Strong ability to assess clinical data and provide medical judgment in complex situations.
• Excellent communication and leadership skills, with the ability to work in a dynamic, fast-paced environment.
• Willingness to travel up to 20% for clinical and regulatory engagements.

• Strategic thinking and problem-solving in clinical development.
• Strong interpersonal and cross-functional collaboration skills.
• Ability to interpret and present clinical data effectively.
• Expertise in regulatory interactions and clinical trial operations.
• Adaptability in a biotech environment with a focus on innovation and efficiency.

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