What are the responsibilities and job description for the Clinical Program Manager position at Eclaro?
Clinical Program Manager
Job Number: 23-00270
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Clinical Program Manager for our client in Summit, NJ - hybrid.
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
- Program Management for the Translational Medicine Leader in support of the Hematology portfolio, driving the development and facilitation of the broad, integrated plans to enable the delivery of our translational medicine portfolio.
Responsibilities:
- Manages complex and high profile portfolio of assets/indications, with broad including both within the corporation and with the external scientific community.
- Execute processes to develop holistic TM plans, manage issues and risk mitigations for the portfolio of assets managed by the TM Scientific Leader.
- Integral partnering with Heme Disease Translational Heads to develop and evolve translational strategies and the tactical project plans to achieve the strategic goals of the team.
- Identification, documentation and management of issues and risks, together with mitigation strategies for the portfolio of assets managed by the translational Leader, primary scope includes: Internal scientific partnerships driving biomarker sub-studies, translational R&D efforts and bioinformatics approaches to scientific evaluation of critical hypotheses, external collaborations for data acquisition, analysis and study activities, publications and presentations (internal and external), and regulatory responses and interactions.
- Establishing communication channels and meeting agendas to drive translational portfolio delivery and documenting outcomes, decisions, and key learnings to enhance collaboration and communication.
- Overseeing the consistency, integrity, completeness, and internal dissemination of biomarker data generation following review of results.
- Supporting efforts to curate and integrate datasets (biomarker results, sample characteristics, clinical outcome) to facilitate analysis, e.g. via Spotfire or other data visualization capabilities.
- Driving biomarker analysis activities, including but not limited to, facilitating data transfer specification creation in collaboration with technical leads, and coordination with both internal and external partners to support biomarker sample movement – as needed.
- Creating visibility and maintaining transparency into collaborative activity that contributes to the translational plan for the key questions.
- Coordinating the evaluation of proposals and ensuring delivery to appropriate collaboration team within expected timelines.
- Elaborating and ensuring effective execution of a robust process for regular program and portfolio strategy reviews facilitated by scientific translational staff.
- Provides scientific leadership in one or more critical areas and "chief of staff" support for key translational leader to enhance operational connectivity and forge a development path into other scientific disciplines bringing enriched operational expertise
Qualifications:
- B.S., M.S., PhD in a scientific discipline; candidates with acceptable program/project management experience will be considered; PMP or equivalent experience is desirable.
- 8 years pharmaceutical industry experience in a variety of operational/scientific roles minimum; 5 years' experience as a matrix leader in a highly diversified environment.
- Experience in Translational Medicine, drug development and biomarkers.
- Experience designing and leading complex, global projects comprised of virtual team members of diverse styles, driving to successful outcomes with and without direct management responsibilities.
- Experience in developing and implementing processes and systems designed to simplify operational infrastructure; including experience with necessary change management skills needed to embed change.
- Experienced in developing and implementing agile, creative solutions, utilizing.
- Thorough understanding of biomarkers and Translational Medicine activities as well as drug development
- Works with a sense of urgency and experience managing multiple projects, building structure from ambiguity and helping teams to develop priorities.
- Drives effective contract/fiscal management of project activities; experienced with the development of business cases for options based decision-making and effective vendor management for externally contracted work.
- Skilled listener with ability to manage complex internal - up, across, and down the hierarchy - and external relationships through constructive conflict management; experience with third party governance oversight desirable.
- Negotiates an enterprise (vs. functional) perspective across the corporation.
- Strong communicator experienced with influencing and interacting at all levels including with senior scientific, operational or external thought leaders to drive connectivity and efficiency of collaborative research.
Job Types: Full-time, Contract
Salary: $100.00 - $109.00 per hour
Medical specialties:
- Oncology
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Ability to commute/relocate:
- Summit, NJ 07901: Reliably commute or planning to relocate before starting work (Preferred)
Application Question(s):
- Do you have pharmaceutical experience?
Work Location: One location
Salary : $100 - $109