Role Description
This role will be within an exciting US based Biotech, an exciting growth company founded on the vision of creating best-in-class cancer therapies. It is an oncology-focused biopharmaceutical company leveraging its deep cross-discipline expertise to discover highly differentiated therapies and develop a broad portfolio of novel combinations addressing significant unmet needs.
You will be part of a medical team that strives to be known for their credibility, tenacity, and urgent focus to collaborate with all stakeholders and improve the lives of patients with cancer.
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A professional with a strong oncology focus and background in scientific engagement.
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The medical expert and point of contact within assigned countries.
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Understanding of the healthcare system within your country and a treatment landscape, diagnostic testing, and reimbursement.
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Collaborates with clinical trial investigators to increase trial enrolment.
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Engages in highly credible scientific discussions with targeted thought leaders (TLs).
Qualifications
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An advanced doctoral degree (MD, PHD, Pharm D) is preferred.
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Post graduate oncology experience is preferred with strong preference for experience working with renal cell carcinoma/RCC.
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3+ years of previous industry medical affairs experience required, preferably in MSL and/or headquartered based medical affairs role.
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Knowledge of healthcare system and understanding of oncology treatment landscape, diagnostic testing, and reimbursement in your country/assigned region.
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Demonstrated expertise in building relationships and participating in credible scientific exchange with multiple audiences within oncology.
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Networking skills and confidence to interact with senior experts on a peer-to-peer level.
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Experience with clinical trial design, conduct, and evaluation.
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Thorough knowledge of local legal, regulatory, and compliance regulations and guidelines relevant to industry interaction with health care professionals.
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Strong written and verbal communication skills, ability to present medical/scientific information in a clear and concise manner.
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Ability to function well, both independently and within a team setting, in a dynamic, fast-paced environment.
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Biotech experience is a plus.
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Fluent in English and fluency in the language of a local country is required.
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Able to travel internationally, up to ~50-70% of time.
Requirements
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Operate in a highly ethical manner and comply with all laws, regulations, and policies.
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Complete mandatory training in assigned timelines upon hire as well as when new policies, SOPs, guidance are issued.
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Adhere to internal standard processes and comply with regulatory and compliance requirements.
Benefits
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We are an equal opportunities employer.
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We encourage and support equal employment opportunities for all applicants.
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Employment decisions are evaluated based on an individual's skills, knowledge, abilities, and qualifications.