Clinical Research Site Manager - TX

Proclinical; San Antonio (TX); On-site; USD 110,000 - 140,000; Full time

Job summary

Proclinical is seeking a Clinical Research Site Manager in San Antonio, TX to lead day-to-day site operations and drive performance.

You will partner with Principal Investigators, manage staff, oversee recruitment, training, and ensure compliance with SOPs and FDA guidelines.

This permanent role offers growth opportunities within a global life sciences services company.

Qualifications

• Proven years of working 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.

Responsibilities

• Operational Planning: Review studies with the Principal Investigator to guide decisions and staffing needs.
• Clinic Operations Management: Hire and develop staff; ensure qualified, trained site personnel.
• Quality Control: Ensure adherence to SOPs, FDA regulations and Good Clinical Practice.

Skills

Clinical Research Experience

Leadership / Supervisory

Regulatory / FDA-GCP

Educational Degree Preferred

Education

Bachelor's degree in a relevant field

Job description

Clinical Research Site Manager - Permanent - San Antonio, TX

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 to be responsible for effectively managing day-to-day site activities for optimization of site performance as well as driving the site to achieve company goals.

Primary Responsibilities:

The Site Manager is responsible for ensuring contractual obligations are met and work is completed in a manner that leads to client satisfaction. It is the responsibility of the Site Manage to work with Leaders to problem solve issues that may arise that interfere with achieving company goals. It is imperative to represent himself/herself and the site in the most professional, ethical and positive manner.

Skills & Requirements:

• Proven years of working 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

The Clinical Research Site Manager's responsibilities will be:

Operational Planning:

• Review and discuss awarded studies with the Principal Investigator to assist Leaders in making informed decisions about what studies to conduct
• Work with Leaders to make informed decisions regarding new staff needs for successful study conduct
• Work with Leaders to ensure site has proper space, staff, and time to optimize study conduct, particularly participant recruitment and retention

Clinic Operations Management:

• Work closely with Leaders regarding staff management
• Demonstrate knowledge of research, expectations, and industry standards o 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
  

Quality Control:

• Manage site quality control process
• Monitors adherence to SOPs and takes immediate corrective actions as necessary to ensure compliance
• Monitors site staff to ensure highest quality performance and adherence to Good Clinical Practice and FDA Regulations and guidance's. Takes immediate corrective actions as necessary to ensure compliance