Site Manager

Job Description

The Site Manager is responsible for operational planning, clinic operations management, investigator relationship development, quality control management, and general responsibilities including communication and coordination.

• Work with Tekton Leaders to make informed decisions regarding new staff needs for successful study conduct.
• Ensure site has proper space, staff, and time to optimize study conduct, particularly participant recruitment and retention.
• Lead staff in continued growth and excellent performance.
• Hire quality candidates for positions within the site.
• Ensure site staff is qualified and trained for roles and duties.
• Work with Tekton Leaders to plan for upcoming studies.
• Ensure site staff and investigators are apprised of awarded studies.
• Maintain medical license(s), certifications, etc.
• Manage study supplies.
• Ensure study closeout activities are completed efficiently.

Required Skills/Abilities

• Communicate in verbal and written form effectively.
• Read or learn to read scientific language and generalize information.
• Able to adhere to instructions and regulations.
• Demonstrate leadership skills.

Education and Experience

• 3+ years’ experience in the Clinical Research Industry.
• Supervisory/management experience or demonstrated definitive leadership skills.
• Experience with regulatory processes, clinical procedures, sponsor interaction, and human resources preferred.
• College or Specialized Degree preferred.