Clinical Research

Lange Recruiting•Richmond, VA

About The Position

The Clinical Research Site Manager oversees clinical research operations across the Richmond, Virginia market, primarily at an established private endocrinology practice, with additional oversight of studies at a local pediatric practice. This hands-on leadership role combines team management with active support of clinical research activities, including stepping in to coordinate trials and assist with participant visits when needed. The manager works with physicians, practice leadership, sponsors, CROs, and organizational leadership to ensure successful study execution, develop staff, and support market growth.

Requirements

At least 3 years of clinical research experience, including substantial hands-on experience coordinating clinical trials.
Prior supervisory or management experience, or demonstrated leadership abilities.
Strong understanding of clinical research operations, regulatory requirements, GCP, and FDA guidelines.
Experience working with Principal Investigators, sponsors, CROs, and clinical research staff.
Ability to train and support Clinical Research Coordinators and independently coordinate studies when needed.
Excellent organizational, communication, problem-solving, and interpersonal skills.
Self-motivated, adaptable leadership style and ability to thrive in a collaborative, fast-paced environment.

Nice To Haves

College degree in a healthcare, science, or related field.
Experience with endocrinology or pediatric clinical trials.

Responsibilities

Oversee daily clinical research operations across the Richmond market, ensuring efficient study execution, strong performance, and high-quality patient care.
Supervise, train, mentor, and evaluate Clinical Research Coordinators.
Support coordinators and step in to coordinate trials, manage participant visits, and assist with study activities as needed.
Develop working relationships with Principal Investigators, medical practice leadership, sponsors, and CRO leadership.
Manage clinical trials from start-up through closeout, ensuring adherence to protocols, timelines, and regulatory requirements.
Develop and implement strategies to meet participant recruitment and retention goals.
Ensure compliance with Good Clinical Practice (GCP), FDA regulations, ICH guidelines, and company policies.
Collaborate with organizational leadership to evaluate new studies, staffing needs, resource allocation, and opportunities for growth.