CenExel · 10 hours ago
Clinical Trial Manager
Marlton, NJ
Full-time
Onsite
Mid, Senior Level
$97K/yr - $115K/yr
3+ years expCenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. The Clinical Trial Manager is responsible for the management of clinical research studies and the personnel assigned to those studies, ensuring successful execution and adherence to protocols.
Clinical TrialsHealth CarePharmaceutical
Responsibilities
Manages all assigned clinical staff
Reads and understands assigned protocols and leads and interfaces on such protocols with the study staff to achieve successful execution within appropriate timeframes
Conducts Site Qualification Visits, as assigned. Schedules and oversees Investigator Meeting arrangements, conducts initiation, study start-up, and team meetings. Oversees scheduling and conduct of monitor visits. Represents the clinical team during site visits
Oversees preparation of, or personally prepares study-specific source documents for new protocols. Reviews and modifies sponsor-provided source documents, when necessary. Assists Study Coordinators in duties, as necessary
On assigned protocols, assists to oversee delivery, shipment, inventory, storage, calibration and accountability of investigational products, supplies and equipment required to conduct clinical investigations
Ensures optimum team function by assisting Clinical Research Coordinators with site start up, enrollment and study execution. Is present for first patient randomized on each study
Fields protocol questions from Clinical Research Coordinators
Acts as the project lead, liaising between sites, investigators, monitors, clinical research coordinators, physicians, laboratory, pharmacy staff, and other study team members. Assists with study in-services and other training needs as needed
Oversees the following aspect of trials but is not limited to: Vendors, Client Satisfaction, Recruitment, Quality, Study Start-up and Trial Outcomes
Monitoring the progress and completion of routine action items and ensuring timely follow-up
Ensuring proper internal procedures are followed and documentation is obtained from coordinators for approval of retest, unscheduled visits, admits, AE treatments, etc
Hires, trains, supervises, and evaluates personnel. Champions and enforces the strictest adherence to best practices, FDA Code of Federal Regulations, ICH (International Conference on Harmonization), GCP (Good Clinical Practices), CenExel standard operating procedures, site Working Practices, protocol, and company guidelines and policies. Retrains and implements corrective and preventative actions, as needed
Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive
Qualification
Required
Bachelor's degree in related field or equivalent experience is preferred
Minimum of three years of Clinical Research Coordinator or equivalent experience
Ability to independently coordinate and manage complex protocols and to lead, motivate and train a clinical research team
Experience managing and leading staff and implementing personnel procedures
Professional image, upholding the company vision in actions, demeanor, and appearance
Must be able to effectively communicate verbally and in writing
Benefits
Health Insurance
Dental
Vision
LTD
STD
Life Ins
401k
Company
CenExel
CenExel is a clinical research site network supporting phase I-IV clinical trials. It is a sub-organization of Webster Equity Partners.
1001-5000 employees
Funding
Current Stage
Late StageTotal Funding
unknown2025-04-12Acquired
2023-04-01Private Equity
Leadership Team
Patrick McLaughlin
Chief Operating Officer
Recent News
2026-02-05
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