Act as primary liaison to investigators interested in developing and performing investigator sponsored trials;
Engage with external experts on the generation of scientific data, including investigator – initiated studies;
Collaborate with clinical organization to enhance patient enrolment in company sponsored clinical trials by identifying appropriate trial sites and interacting with investigators in on going trials;
Gather careful information from KOLs and report back to company to help develop clinical, as well as commercial strategy.
Deeply understand the unique oncology treatment paradigm, key stakeholders, and healthcare landscape in your territory;
Develop and execute territory plans in alignment with medical strategy.
Opinion Leader Engagement
Identify, develop and maintain collaborative relationships with current and future Key Opinion Leaders (KOLs) and healthcare stakeholders in disease states of strategic importance to the company;
Provide medical and scientific information to respond to KOLs’ technical questions about the molecule/drug;
Represent client at select scientific congresses and professional society meetings;
Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, and healthcare provider setting in both group and one on one settings.
Cross Functional Support
Assist as needed to local tactical activities (coverage of presentations at select scientific congresses, knowledge of contracting local consultants, etc.);
Assist in the reconnaissance of Market landscape determination and competitive intelligence including therapeutic trends and unmet needs within the appropriate disease states and marketplace and provide timely feedback/information on emerging clinical/scientific information to internal stakeholders.
Operate in a highly ethical manner and comply with all laws, regulations and policies;
Complete mandatory training in assigned timelines upon hire as well as when new policies, SOP’s, guidance are issued;
Adhere to internal standard processes and comply with regulatory and compliance requirements.
Doctorate level degree or equivalent experience is required (PharmD, PhD, MD, MSN);
Post graduate oncology experience is required with preference for experience working with lung cancer;
3+ years of previous industry medical affairs experience required, preferably in MSL and/or headquartered based medical affairs role;
Knowledge ofhealthcare system and understanding of oncology treatment landscape, diagnostic testing and reimbursement in your country/assigned region;
Demonstrated expertise in building relationships and participating in credible scientific exchange with multiple audiences. Networking skills and confidence to interact with senior experts on a peer to peer level;
Experience with clinical trial design, conduct and evaluation;
Thorough knowledge of local (several countries or territory) legal, regulatory, and compliance regulations and guidelines relevant to industry interaction with health care professions;
Strong written and verbal communication skills, ability to present medical/scientific information in a clear and concise manner;
Ability to function well, both independently and within a team setting, in a dynamic, fast-paced environment. Team orientated and ability to work collaboratively towards common objectives;
Biotech experience is a plus;
Fluent in English and fluency in the language of a local country is required;
Able to travel internationally, up to ~50-70% of time.