Research Industry Partners Liaison
3 days ago
As an Industry Liaison at ECOG-ACRIN MRF, your primary responsibilities will include:
- Coordinating Pharmaceutical Industry-related activities within our operations office, including collaboration with grants and contracts team, clinical operations team, protocol development team, lab science team, data management and statistical teams.
- Coordinating Pharmaceutical Industry-related activities outside our operations office, including collaboration with our Pharmaceutical Industry partners, ECOG-ACRIN Headquarters, NCI/CTEP/DCP, and study and committee chairs.
- Participating in business development activities.
- Assisting with negotiation of contracts with Pharmaceutical Industry partners, including providing ECOG-ACRIN contracts office with approved scopes of work, budgets, and review of draft contracts.
- Assisting in establishing costs used in study budgets.
- Tracking contract deliverables due to our Pharmaceutical Industry partners for executed agreements, including monitoring of timelines and deliverables.
- Pharmaceutical Industry portal submission updates for accrual, drug request, any protocol amendments.
- Developing and delivering presentations such as (not limited to) ECOG-ACRIN overview, concept submission process, collaborations, and study status.
- Coordinating participation of Outside US (OUS) countries on ECOG-ACRIN protocols.
- Managing third party drug distributors and other vendors.
Requirements
A minimum of 5 years of experience in clinical trials (oncology experience required). Management experience along with knowledge of clinical operations and business development activities. Experience and knowledge of grants, budgeting, and contracts. Experience and knowledge of protocol development process. Experience and knowledge of NCI / cooperative group trials. Experience in working with Pharmaceutical Industry partners. Bachelor's degree from an accredited college or university is required. RN and or RPh/PharmD preferred.
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