Clinical Research Site Manager - TX

Proclinical; San Antonio; On-site; CLP 83,415,000 - 127,576,000; Full time

Job summary

Proclinical is seeking a Clinical Research Site Manager to lead day-to-day site activities, optimize performance, and drive studies to meet sponsor and company goals. The role emphasizes fulfilling contractual obligations while upholding quality and ethics.

You will work with Leaders to plan studies, recruit and train staff, monitor regulatory compliance, and oversee site operations, quality control, and participant safety.

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 on which studies to conduct.
• Team staffing: Assess staff needs for successful study conduct and ensure proper resources.
• Clinic Operations: Manage site staff, ensure qualifications, and train roles and duties.

Skills

Clinical research experience

Leadership

Regulatory knowledge

Staff management

Education

College or specialized degree

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

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