Industry Liaison
3 weeks ago
Industry Liaison (Oncology Studies)
Summary: Working under the direction of the Senior Director, Clinical Research, the Industry Liaison will be responsible for assisting with liaison activities between ECOG-ACRIN Medical Research Foundation (“EAMRF”) and our pharmaceutical industry partners during all stages of a clinical trial, from development to study closeout.
Key Responsibilities:
- Coordinate Pharmaceutical Industry related activities within the EAMRF Operations office, including collaborating with grants and contracts team, clinical operations team, protocol development team, lab science team, data management and statistical teams
- Coordinate Pharmaceutical Industry related activities outside the EAMRF Operations office, including collaborating with our Pharmaceutical Industry partners, the EAMRF Headquarters, NCI/CTEP/DCP and study and committee chairs
- Participates in business development activities
- Assists with negotiation of contracts with Pharmaceutical Industry partners, including providing the EAMRF contracts office with approved scopes of work, budgets and review of draft contracts
- Assist in establishing costs used in the study budgets
- Track contract deliverables due to our Pharmaceutical Industry partners for executed agreements, including the monitoring of timelines and deliverables
- Pharmaceutical Industry portal submission updates for accrual, drug request, any protocol amendments
- Develops and delivers presentations such as (not limited to) ECOG-ACRIN overview, concept submission process, collaborations, and study status
- Coordinate participation of Outside US (OUS) countries on ECOG-ACRIN protocols
- Manage third party drug distributors and other vendors
- Other duties as assigned
Experience
- Minimum of five (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
Education
- Bachelor's degree from an accredited college or university is required.
- RN and or RPh/PharmD preferred
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