Study Activation Specialist
About The Position
As the Study Activation Specialist, you are responsible for managing the startup activities of clinical trials proposed and entering those trials into the Sarah Cannon Strategic Sites’ clinical research program menus. You will maintain relationships and facilitate progress across multiple groups including but not limited to internal SC departments, Strategic Sites physicians and staff, Contract Research Organizations (CROs), and Pharmaceutical Companies. You will serve as the primary responsible party and point of contact during clinical research trial feasibility, planning, and implementation stages up until the point of site activation.
Requirements
- High School Diploma required
- Knowledge of pharmaceutical industry, regulatory processes, clinical trials and medical terminology
- The availability to travel occasionally
- At least one year of experience in Customer Service in a Client Facing Role
Nice To Haves
- Bachelor Degree preferred
- Experience in healthcare, research, pharmaceutical or marketing industries preferred
Responsibilities
- Develop relationships with sponsors and (CROs), which provide potential studies
- Maintain a database of potential pharmaceutical and CRO relationships
- Market Sarah Cannon services and capabilities to pharmaceutical companies, CROs and within the industry network
- Develop and maintain strong industry ties, utilizing both the network and the Internet, in order to acquire new studies
- Provide information and updates on current studies in the start-up process at all Sponsor meetings
- Track all site metrics relating to the study start up process for each Strategic Site
- Other duties as assigned
Benefits
- competitive compensation package
- annual bonus or long-term incentive opportunities may be offered
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
