Clinical Research Coordinator, On-Site, Horsham, Pennsylvania

IQVIA•Hatboro, PA

1d•$36,600 - $91,300•Onsite

About The Position

Please note this position is fully on-site position at the site in Horsham, PA Join a collaborative, patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role — it’s a unique opportunity to deepen your expertise in clinical trial coordination, grow within a supportive environment that values professional development, and make real progress toward your career goals. It’s an ideal fit for a hardworking, driven, and passionate individual who thrives in a fast-paced, team-oriented setting and is eager to make a meaningful impact through clinical research. Overview: Coordinate and participate in clinical research studies ensuring that studies are carried out according to protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.

Requirements

Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Clinical Research Coordinator experience within a similar setting
Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
Knowledge and experience of site operations and the drug development process
Effective communication
Computer proficiency in use of Microsoft Word, Excel

Responsibilities

Coordinate clinical research studies conducted by a supervising principle investigator.
May assist as back-up CRC on other studies
Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
Obtains informed consent of research subjects
Develops strong working relationships and maintain effective communication with study team members
Completes all protocol related training
Performs patient/research participant scheduling
Collects patient/research participant history
Collects and maintains source documentation
Manages inventory and administers test articles/investigational product to participants
Performs data entry and query resolution
Supports the collection and review of required essential study documents and reports.
Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging, and laboratory handling manuals, etc.)
Adheres to an IRB approved protocol
Supports the safety of research subjects, report adverse events
Coordinates protocol related research procedures, study visits, and follow-up
Facilitates pre-study, site qualification, study initiation, monitoring visits, and study close out activities
Collects, processes and ships laboratory specimens
May be asked to perform special project responsibilities and travel to other clinic locations, within the area, when needs arise
Complies with Avacare and Sponsor policies, standard operating procedures (SOPs) and guidelines
Performs other duties as assigned