A pharmaceutical client is seeking a Clinical Study Coordinator to support Oncology clinical research trials. This is a 4-month PART-TIME, CONTRACT assignment.
This individual should be able to commit to at least 3 days per week of work, all of which will be onsite. The workload could ebb and flow by week, and could increase, and could also be just 2 days some weeks.
Responsibilities include day-to-day trial management such as tracking study progress, following up with sites and vendors, managing timelines and deliverables, and ensuring adherence to Good Clinical Practice (GCP) guidelines and Sponsor requirements.
The Consultant will assist with vendor and site selection, review study documents and protocols, support the development of operational plans, and serve as a key liaison between the Sponsor and CROs. Duties also include oversight of the Trial Master File (TMF), monitoring study documentation, attending regular study meetings, addressing operational issues as they arise, and supporting data review and regulatory submissions.
QUALIFICATIONS & REQUIREMENTS:
5-10 years of relevant experience as a lead clinical study coordinator (or sole study coordinator) for early phase oncology trials for clinical study site(s)
Good quality control, and written, verbal and interpersonal communication skills and computer and EDC proficiency
Experience as an oncology Clinical Research Nurse is a big plus
LOCATION:
Work will be performed onsite in the greater Baltimore Maryland area.