- Clinical research jobs
- VP, Regional Medical & Scientific Affairs
Use our `search` to find similar offers.
VP, Regional Medical & Scientific Affairs
Parexel International Corporation
Shanghai, Shanghai Municipality, China
Job Purpose:
The VP, Regional Medical & Scientific Affairs is responsible for creating and executing in collaboration with the Senior Vice President, Business development & Head of Biotech to achieve goals (NBA) set for the region. As a member of Medical & Scientific Affairs, they will play a key role in expanding the understanding of Parexel Biotech and the specific benefits of the designated biotech to work with the Parexel Biotech vs. a niche CRO or competing biotech divisions of the larger CROs. Day-to-day responsibilities include:
• Interacting directly with senior leaders (C-level) biotech/ pharmaceutical companies to build relationships and advance collaboration.
• Perform the role of Executive Sponsor to key sponsors within the region of responsibility.
• Working with and advising clients/pharmaceutical companies on medical strategies and innovations that inform company direction.
• Advise on all areas of drug development internally and externally.
• Provide drug development knowledge and apply that knowledge to give high-level input to protocol design and medical practice for key proposal preparation.
• Participate in BPMs to provide executive support to the assembled global team.
• Share product development experiences able to assist in guiding biotech clients on how to develop their compound globally – build up the road map with clients together.
• Willing to be a speaker to give a talk and even chair session in DIA Asia or other relevant Biotech or Disease-related conferences including Investment Forums for health sectors.
Key Accountabilities:
Accountability Supporting Activities
• Provide executive and senior leadership with updates on drug development trends future perspectives, challenges, important advances, and relevant growth potential in therapeutic areas related to the region.
• Provides recommendations for how to approach the sponsors and thought leadership (KOLs).
• Develop a strategy for expanding new and repeat business.
• Work with and advise clients/pharmaceutical companies on medical strategies and innovations that inform company direction.
• Interact directly with senior leaders at clients/pharmaceutical companies to build relationships and advance collaboration.
• Leverage medical expertise and industry network for the benefit of Parexel by influencing and interacting with a wide range of Parexel stakeholders.
• Ensure that teams provide appropriate and timely support for commercial, proposal, and/or marketing activities as requested.
Leadership • Maintain a positive, results-oriented work environment that is globally focused, inclusive, collaborative, and respectful.
• Provide leadership and development to franchise colleagues to advance medical and scientific capabilities to ensure their performance meets and/or exceeds both the business and their own personal goals and objectives.
QualificationsSkills:
• Proven ability to work well with small teams, often under significant time constraints.
• Ability to lead, direct and motivate a team of commercial and medical professionals.
• Strong ability to understand implications of recommendations, decisions and their impact on clients, patients and Parexel.
• Experience making presentations at conferences and meetings.
• Business acumen, with understanding of financial and marketing principles.
• Strong communication and interpersonal skills needed to collaborate, negotiate and influence effectively with diverse medical and non-medical stakeholders.
• Fluent in English, with excellent writing skills.
Knowledge and Experience:
• Proven and applied expertise in clinical drug development at a senior level position (VP of Operations, R&D, in the CRO and/or pharmaceutical industry.
• Previous CMO of a Biotech preferred but not necessary.
• Prior academic/clinical patient care experience within the TA.
• Experience in clinical research, as an investigator or sub-investigator; but not mandatory.
• Experience with relevant regulatory requirements and guidelines for drug development in the Region they in which they are applying to work.
Job posted: 2021-12-29