À±½·ÊÓÆµ

Site Manager

Highly Competitive
  1. Permanent
  2. VP/Head of Clinical Operations
  3. United States
St. Louis, USA
Posting date: 06 May 2026
69468

Site Manager - Permanent - St Louis, Missouri

Ready to oversee a site that helps bring life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!

À±½·ÊÓÆµ is seeking a Site Manager to oversee and optimize day-to-day site activities, ensuring smooth operations and alignment with organizational goals.

Primary Responsibilities:

In this role, you will work closely with leadership, staff, and participants to ensure high-quality clinical research practices while maintaining compliance with industry standards. This position requires a proactive approach to problem-solving and a commitment to fostering a professional and ethical work environment.

Skills & Requirements:

  • Strong knowledge of clinical research expectations and industry standards.
  • Proven leadership skills with experience in staff management and development.
  • Familiarity with regulatory processes, clinical procedures, and sponsor interactions.
  • Ability to manage human resources effectively within a clinical research setting.
  • College degree or specialized training preferred.
  • Experience in the clinical research industry, with a focus on quality control and operational management.

The Site Manager's responsibilities will be:

  • Collaborate with the Principal Investigator and leadership to evaluate and plan awarded studies.
  • Assist in decision-making regarding staffing needs and resource allocation for successful study execution.
  • Ensure the site has adequate space, staff, and time to optimize participant recruitment and retention.
  • Oversee clinic operations, including staff management and performance development.
  • Lead hiring efforts to recruit qualified candidates and ensure proper training for all site staff.
  • Manage quality control processes, ensuring adherence to SOPs, Good Clinical Practice (GCP), and FDA regulations.
  • Take immediate corrective actions to address any compliance or performance issues.
  • Monitor and maintain high standards of site performance and client satisfaction.

If you are having difficulty in applying or if you have any questions, please contact Alex Kelly at a.kelly@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

À±½·ÊÓÆµ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓÆµ is acting as an Employment Agency in relation to this vacancy.

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