First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Permanent

Discipline: CRA Manager

Location: United States

Clinical Research Site Manager - Permanent - Midlothian, VA

Ready to be the heartbeat of medical research? Join our client as a Site Manager and assist in turning innovative science into life-changing care!

̽��ϼ� is seeking a Clinical Research 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 working 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

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

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@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.

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

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - /privacy-policy