Oncology Clinical Trials Activation Lead

McKesson Corporation; Tennessee; On-site; USD 65,000 - 90,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Study Activation Specialist to manage startup activities for proposed clinical trials across multiple sites. You will coordinate with internal departments, CROs, and sponsors, guiding trials from feasibility to site activation.

You will develop sponsor relationships, market SCRI services, and track startup metrics, contributing to the efficient launch of studies nationwide. A focus on collaboration and regulatory literacy is essential.

Qualifications

• High School Diploma required; Bachelor Degree preferred.
• Knowledge of pharmaceutical industry, regulatory processes, clinical trials and medical terminology.
• Willingness to travel occasionally.
• At least one year of experience in Customer Service in a Client Facing Role.
• Experience in healthcare, research, pharmaceutical or marketing industries preferred.

Responsibilities

• Manage startup activities of clinical trials proposed and entering those 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 primary responsible party and point of contact during clinical research trial feasibility, planning, and implementation up until site activation.
• Develop relationships with sponsors and CROs to identify potential studies.
• Market Sarah Cannon services and capabilities to pharmaceutical companies, CROs and within the industry network.
• Track site metrics relating to the study start up process for each Strategic Site.
• Other duties as assigned.

Skills

Customer service

Relationship building

Communication skills

Travel readiness

Education

High School Diploma

Bachelor's degree preferred

Job description

Sarah Cannon Research Institute (SCRI) is seeking a Study Activation Specialist to manage startup activities for proposed clinical trials across multiple sites. You will coordinate with internal departments, CROs, and sponsors, guiding trials from feasibility to site activation.

You will develop sponsor relationships, market SCRI services, and track startup metrics, contributing to the efficient launch of studies nationwide. A focus on collaboration and regulatory literacy is essential.