Clinical Research Site Manager / Clinical Research Site Manageress

Clinical Research Site Manager - Permanent - San Antonio, TX

Are you ready to lead a clinical research site that brings life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!

Proclinical is seeking a Site Manager who will be responsible for effectively managing day-to-day site activities to optimize performance and drive the site toward achieving company goals.

Primary Responsibilities

The Site Manager is pivotal in ensuring that contractual obligations are met and work is completed in a manner that leads to client satisfaction. You will be expected to collaborate with Leaders to resolve issues that may arise and impede the achievement of company goals. Representing yourself and the site in the most professional, ethical, and positive manner is imperative.

Skills & Requirements

• Proven years of working experience in the Clinical Research Industry
• Supervisory or management experience, demonstrating definitive leadership skills
• Experience with regulatory processes, clinical procedures, sponsor interaction, and human resources preferred
• College or Specialized Degree preferred

Key Responsibilities

Operational Planning

• Review and discuss awarded studies with the Principal Investigator to assist Leaders in making informed decisions about which studies to conduct.
• Collaborate with Leaders to assess new staffing needs for successful study conduct.
• Ensure the site has adequate space, staff, and time to optimize study conduct, particularly for participant recruitment and retention.

Clinic Operations Management

• Work closely with Leaders on staff management.
• Demonstrate knowledge of research, expectations, and industry standards.
• Guide staff towards continued growth and excellent performance.
• Hire quality candidates for positions within the site.
• Ensure site staff is qualified and trained for their roles and responsibilities.

Quality Control

• Manage the site quality control process.
• Monitor adherence to SOPs and take immediate corrective actions as necessary to ensure compliance.
• Oversee site staff to ensure the highest quality performance, adherence to Good Clinical Practice, and compliance with FDA regulations and guidelines.

If you are interested in applying to this exciting opportunity, please apply online using the form below. Only applications matching the job profile will be considered.

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

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