Closed
Remote - Boston MA
Posted 2 years ago
Consulting Position – Long term – Remote
This position will lead the development of a strategic integrated evidence-generation plan. Partner with GPT Evidence Generation sub-team (a multidisciplinary team), to develop/optimize the integrated strategic evidence generation initiatives across therapeutic areas, proactively anticipating any potential gaps and adjusting tactical plans to address these.
Responsibilities:
- Responsible for post-approval research excellence within the CMO.
- Supports the development of a strategy for all study types within the CMO, i.e., sponsored studies (MACs), Collaborative Research, and IIRs.
- Provides innovative thinking and scientific expertise into post-approval research programs and real-world evidence strategies.
- Supports strategic discussions for each assigned therapeutic area to identify research gaps and develop aligned strategic and tactical plans to address these gaps and works closely with GMA GPT representatives and partners responsible for executing evidence generation plan.
- Drives, builds, and maintains the strategic evidence generation plans, closely partnering with the GML, PVPA and GORE with input from multiple stakeholders (regions, SQS, etc).
- Establishes GMA framework (i.e. subteam to asset strategy team) to support evidence generation needs.
- Collaborates with cross-functional team members to define global evidentiary needs of key stakeholders (Regulatory bodies, HCPs, Patients/caregivers, Payers, and HTA bodies) to serve the evolving healthcare environment.
- Supports collaborative strategic planning and mapping of evidence-generation activities with key internal stakeholders to develop aligned and integrated generation strategies and plans.
- Provides strategic leadership and scientific direction on medical evidence activities in order to: Set standards for the utilization of medical data and maximize patients’ access to our innovative medicines.
- Participates as a functional expert on other cross-functional leadership teams.
Requirements:
- Minimum MSc degree required (preferably PhD), preferably in a health sciences-related field with 6 years of research-related experience and/or pharmaceutical industry experience.
- Experience with late-stage clinical studies, research collaborations and RWE.
- Proven track record of strong leadership, and project management and demonstrated ability to coach and mentor individuals.
- Ability to communicate and interact thoughtfully, transparently, and appropriately with a variety of stakeholders, both internal and external.
- Experience overseeing work of and mentoring other individuals with a variety of scientific and non-scientific backgrounds and training.
- Experience working in a global organization and within a matrix structure is highly desirable.
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Job Features
Job Category | Regulatory - Global Evidence Generation |
Reference Number | 201140 |