Study Activation Specialist - Remote

Overview

The Study Activation Specialist at Sarah Cannon Research Institute plays a crucial role in managing the startup activities of clinical trials, facilitating relationships with various stakeholders to enhance oncology treatments and improve patient outcomes.

In Short

• Manage startup activities of clinical trials.
• Serve as the primary contact during trial feasibility and planning.
• Develop and maintain relationships with sponsors and CROs.
• Market Sarah Cannon services to pharmaceutical companies.
• Track site metrics related to the study startup process.
• Provide updates on current studies at Sponsor meetings.
• Maintain a database of potential pharmaceutical and CRO relationships.
• Occasional travel may be required.
• High School Diploma required; Bachelor Degree preferred.
• Experience in healthcare or pharmaceutical industries preferred.

Requirements

• Knowledge of pharmaceutical industry and clinical trials.
• At least one year of customer service experience.
• Strong communication and relationship-building skills.
• Ability to work independently and as part of a team.
• Proficiency in database management and marketing.

Benefits

• Comprehensive benefits to support physical, mental, and financial well-being.
• Competitive compensation package based on performance and experience.
• Opportunities for professional growth and development.
• Inclusive work environment with strong values.