Oncology Clinical Trials Startup Specialist (Equity Options)

McKesson’s Corporate; Tennessee; On-site; USD 60,000 - 80,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Study Activation Specialist responsible for kickoff and startup activities of clinical trials initiated through the Sarah Cannon Strategic Sites program. You will manage sponsor and CRO relationships and guide studies from feasibility through activation.

The role requires a High School Diploma, with a Bachelor Degree preferred, strong knowledge of the pharmaceutical industry and regulatory processes, and occasional travel.

Qualifications

• High School Diploma required; Bachelor Degree preferred.
• Knowledge of pharmaceutical industry, regulatory processes, clinical trials and medical terminology.
• The availability to travel occasionally.

Responsibilities

• Manage startup activities of clinical trials and enter trials into the Sarah Cannon Strategic Sites’ clinical research program menus.
• Maintain relationships and facilitate progress across multiple groups including internal SC departments, Strategic Sites physicians and staff, CROs, and Pharmaceutical Companies.
• Serve as the primary responsible party and point of contact during feasibility, planning, and implementation stages up until site activation.
• Market Sarah Cannon services and capabilities to pharmaceutical companies, CROs and within the industry network.
• Track site metrics related to the study start up process for each Strategic Site.

Skills

Customer Service

Healthcare knowledge

Networking

Travel coordination

Education

High School Diploma

Bachelor Degree preferred

Job description

Sarah Cannon Research Institute (SCRI) is seeking a Study Activation Specialist responsible for kickoff and startup activities of clinical trials initiated through the Sarah Cannon Strategic Sites program. You will manage sponsor and CRO relationships and guide studies from feasibility through activation.

The role requires a High School Diploma, with a Bachelor Degree preferred, strong knowledge of the pharmaceutical industry and regulatory processes, and occasional travel.