Senior Medical Director– Oncology - Mid-sized CRO – Homebased USA
REMOTEPosted 30+ days ago
Job summary
Job post source
This job is from a recruiting firm hiring for a separate company.
Job overview
The Senior Medical Director– Oncology role at a mid-sized CRO involves leading scientific and clinical strategy for oncology clinical trials, ensuring quality data and medical oversight.
Responsibilities and impact
The role requires providing medical expertise to clinical project teams and sites, advising clients and regulatory bodies, collaborating on protocol development, reviewing clinical documents, and participating in key meetings.
Experience and skills
Candidates must have a Medical Doctor degree, board certification or fellowship in Oncology, experience with solid or hematological tumors, and client-facing experience in a CRO or pharmaceutical/biotech environment; CAR-T and cell therapy experience is a plus.
Company information
The job is for a global mid-sized CRO client represented by i-Pharm Consulting, a recruiting firm.
Job location and travel
This is a full-time, home-based position anywhere in the USA.
Application process
Interested candidates should contact Aoife Cronin at acronin-pharmconsulting.com to apply.
Company overview
i-Pharm Consulting is a global recruitment firm specializing in the life sciences sector, providing staffing solutions for pharmaceutical, biotechnology, and medical device companies. They generate revenue through recruitment services, including permanent and contract placements, leveraging their extensive industry network and expertise. Founded in 2008, i-Pharm has grown significantly, establishing offices in key locations such as London, Munich, and Sydney, and earning a reputation for delivering high-quality talent and fostering long-term client relationships.
How to land this job
Position your resume to underscore your medical degree and board certification or fellowship in Oncology, emphasizing your expertise in solid and hematological tumors as well as any experience with CAR-T and cell therapies.
Highlight your experience in clinical strategy, medical monitoring, and client-facing roles within CROs or pharmaceutical/biotech companies, showcasing your ability to collaborate with cross-functional teams and advise regulatory bodies.
Apply through multiple channels including the i-Pharm Consulting corporate website, LinkedIn job postings, and relevant clinical research job boards to maximize your application visibility.
Connect with Senior Medical Directors or Clinical Project Managers at i-Pharm Consulting on LinkedIn; initiate conversations by referencing recent oncology clinical trials they might be involved with or expressing interest in their approach to medical monitoring.
Optimize your resume for ATS by incorporating keywords from the job description such as 'medical monitor,' 'clinical strategy,' 'oncology,' 'CAR-T,' 'clinical trials,' and 'regulatory advising' to ensure your resume passes initial screenings.
Leverage Jennie Johnson's Power Apply feature to automate tailored applications, identify optimal application platforms, and find LinkedIn contacts for networking, allowing you to focus your energy on interview preparation and clinical expertise demonstration.
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