Clinical Research Associate II (Part-time Contract)

• Perform monitoring activities (both on site and remote) including Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, Site Management Contacts, Close Out Visits for Phase I-IV clinical trials.

• Ensure the validity, correctness, and completeness of clinical data collected at sites with a focus on data integrity and patient safety as dictated by trial protocol, ICH-GCP/ISO 141155, and customer requirements.

• Serve as the primary point of contact for investigative sites, manage query resolution, support Trial Master File activities, participate in Investigators’ Meetings, and complete other project tasks in accordance with study timelines and budget.

• Identify and escalate potential risks and possible retraining opportunities for investigative sites.

• Schedule and plan day-to-day activities to include study monitoring visits, timely completion of high quality trip reports, and active management of all deliverables.

What we are searching for:

• Undergraduate degree required or its international equivalent, along with minimum of 2+ years previous clinical research monitoring experience required.

• Known for being customer-focused in approach to work and communications with the ability to professionally interact with sites, clients, vendors and other functional areas

• Experience with monitoring oncology studies highly prioritized

• Accountable, dependable and strong commitment 

• Ability to travel up to 70-85%

• Preferred Location: East Coast

• Please note this is a 12 month 1099 contractor position that will start off part-time with potential to go full-time

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The actual salary will be influenced based on a variety of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.