Senior Medical Director, Hematology/Oncology

This is a fully remote position, open to applicants in United States, +1 more country.

📋 Description

• Deliver scientific, clinical, and operational oversight for global clinical research initiatives.

• Serve as the Medical Monitor and primary medical liaison among IQVIA, sponsors, and investigative sites.

• Provide guidance on protocol interpretation, eligibility criteria, compliance, safety, medical data evaluation, and responses to urgent medical inquiries.

• Offer medical and scientific insights on business proposals, clinical data, protocols, training resources, informed consent documents, Investigator Drug Brochures, eCRFs, analysis plans, clinical study reports, regulatory submissions, and adverse event reporting.

• Ensure that medical activities adhere to GCP standards and operate efficiently.

• Build and maintain a network of medical and scientific consultants.

• Assist in site selection, engage investigators, and strategize patient recruitment and retention.

• Train study teams and investigators on protocols and therapeutic areas.

• Develop and oversee medical monitoring strategies.

• Monitor patient safety and evaluate study safety profiles.

• Review and interpret safety data, including SAEs and critical clinical information.

• Facilitate safety reporting and collaborate with sponsors and internal safety teams.

• Manage unblinding processes and participate in regulatory interactions.

• Review clinical data, including eCRFs, tables, and listings.

• Contribute to data interpretation and the preparation of clinical study reports.

• Support proposal development, feasibility evaluations, and client presentations.

• Provide medical expertise for study design and new business ventures.

• Assist in internal processes, training, and quality enhancement initiatives.

• Contribute to scientific literature reviews and provide medical insights across various projects.

⛳️ Requirements

• MD degree from a recognized, accredited medical school.

• 5–7+ years of clinical experience as a licensed physician in Oncology, Hematology, Surgical Oncology, or Urology with a focus on oncology.

• Board certification or eligibility in the relevant therapeutic area is highly preferred, or equivalent experience.

• Demonstrated experience in clinical research (≥3 years) as a study physician/investigator or within Pharma, CRO, or Biotech settings.

• Proficient in English, with the ability to communicate fluently.

• Strong capability to collaborate effectively within multidisciplinary and matrixed global teams.

• Ability to work independently while juggling multiple priorities in a fast-paced environment.

• Excellent organizational skills with the capacity to manage complex projects amidst changing timelines and requirements.

• Outstanding communication and interpersonal abilities, with the skill to convey complex medical concepts into clear, actionable insights.

🏝️ Benefits

• Global reach and collaboration with international teams.

• Opportunities to engage in internal processes, training, and quality improvement initiatives.