The posting
Who we are…
Nuvation Bio is a biopharmaceutical company tackling some of the greatest unmet needs in oncology by developing differentiated and novel therapeutic candidates. Our vision is to significantly change the practice of oncology by developing medicines that provide truly meaningful improvements in quality of life and survival for people with cancer.
What you’ll be doing
The Regional Medical Director will perform a key role within Medical Affairs, supporting the oncology portfolio, including taletrectinib and safusidenib, through strategic alignment and execution of activities related to investigator/KOL engagement, insight collection, support of investigator and company sponsored trials, medical communications, and cross-functional collaboration. As part of the execution of Nuvation Bio Pharmaceuticals’ strategy, he/she, as a member of Medical Affairs, will work closely with the Clinical Development, Commercial, and Market Access functions.
You will be responsible for…
- Responsible for realization of medical/scientific objectives for the RMD team
- Establish & maintain professional relationships with external experts, academic institutions, community networks, and managed care communities
- Present critical medical and scientific information to external audiences and individuals (such as healthcare professionals, formulary committees, and medical meetings)
- Identify unmet medical, educational, and research needs within the medical community, and make an intelligent interpretation of key relevant scientific data and translate this information to meet educational and research needs
- Collaborate with cross‐functional teams in assessing education/research needs and develop education/research strategies to meet those needs
- Provide medical and scientific support for internal collaborations, such as sales training, speaker bureau training, and other educational initiatives
- Assist in the identification of investigators and sites for company sponsored trials
- Participate in objective setting as well as contributing to the professional development for the RMD team
- Serve as a liaison for the review, submission, execution, completion of ISR (Investigator Sponsored Research) proposals and facilitate the initiation of research projects
- Represent Nuvation Bio at medical meetings, conferences, advisory boards, outreach meetings at key institutions and in interactions with thought leaders
- Maintain knowledge of the lung and neuro oncology fields, stay current on leading edge medicines and development efforts, and provide expertise for business development opportunities as appropriate
- Contribute to & be able to lead select Medical Affairs projects and execution through hybrid Home Office Medical responsibilities
- Assure RMD team compliance with all corporate policies and regulatory guidelines
What Knowledge & Experience you'll bring to us...
- Advanced degree (MD, PhD, PharmD) in a medical or science-related specialty, although significant experience in the medical field may be considered in lieu of an advanced degree.
- Requires at least 4 years of experience as field MSL/RMD with demonstrated excellent communication skills (oral and written)
- A combination of education and experience may be considered
- Strong and established relationships and experience in lung/thoracic oncology preferred
- Solid understanding of drug development and life‐cycle development of a product required
- Understanding of the FDA, Pharma Code and other ethical guidelines relevant to the pharmaceutical industry
- Ability to cultivate and maintain relationships with clinical investigators and key opinion leaders in the relevant fields, and to establish trust through the consistent demonstration of scientific expertise and satisfactory follow‐through to requests from key opinion leaders
- Able to articulate ideas and concepts, be persuasive and have the ability to convey complex, scientific ideas fluently to any audience
- Must utilize effective, professional communications to cultivate and nurture strong working relationships with internal and external colleagues
- Ability to conduct oneself in a highly professional and ethical manner
- A thorough understanding of the clinical trial and investigator initiated study processes
- Ability to multi‐task, work independently and focus on priorities
- Must deal with ambiguity and thrive in an ever‐changing environment
- Must live in assigned region
- Travel minimum 50 % and manage a demanding schedule
Behavioral skills to be successful...
- Problem-Solver - As an action-oriented self-starter, you’re eager to apply your expertise in diagnosing inefficiencies, determining root causes, and recommending solutions to complex challenges.
- Personable - You establish and nurture highly effective relationships with colleagues and key stakeholders that support and advance project goals and objectives.
- Credible - Thorough understanding of clinical methodologies and providing sound analytical support, you quickly establish credibility as a reliable resource.
- Emotional intelligence, curiosity, and a knack to figure out a way to build something better
- Communication - Effectively listens, conveys, and receives ideas. Maintains a consistent flow of information. A strong presenter and effective communicator with the ability to influence stakeholders.
- Accountability - Acts with a clear sense of ownership - whether the task is in their role description. Holds yourself and others accountable to execute all tasks at hand through seen and unforeseen circumstances with high quality and integrity.
- Adaptability - Can manage in an environment of ambiguity. Embraces the change of a new system, process, technology, or idea in the organization. You could reassess priorities, alter goals and take risks.
What we have for you!
- Competitive Base Salary, Bonus, and Equity Plans
- Unlimited Vacation and 10 Sick Days Annually
- Excellent Medical, Dental, and Vision Coverage
- 401K with Company Matching
- and much more!
The base pay offered will take into account internal equity and also may vary depending on the candidate’s job-related knowledge, skills, experience, and location among other factors. Our full-time regular positions also include an annual performance-based bonus and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, depending on the level and position offered.
Disclaimer
Nuvation Bio, Inc. is an equal opportunity employer, and, in accordance with applicable federal, state, and/or local law, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by the law.
This job description reflects the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Nothing restricts management’s right to assign or reassign duties and responsibilities to this job at any time.
Note to all external Recruiters & Staffing Agencies All of our open positions are managed by our Talent Acquisition department. Any resumes submitted through the website or directly by recruiters or staffing agencies in advance of an executed agreement with Nuvation Bio, Inc., will be considered unsolicited and the company will not be responsible for any related fees. Resumes sent directly to employees or hiring managers will also not be accepted as referrals.
