Highlights:

• Adjudication experience is a must
• 6-month contract with possibility of being extended
• Looking to hire ASAP
• Fully remote
• RN is preferred
• Source document review
• Discharge summaries and lab report experience
• Ability to work/communicate with sites
• Candidates with previous CRO experience are highly preferred

Clinical Trials Coordinator II / Clinical Event Classification (CEC) Coordinator II / Clinical Events Committee

Occupational Summary:

The CTC II develops, coordinates and implements the management of the clinical endpoint adjudication process for clinical trials research conducted by Principal Investigator(s). The CTC II also performs a variety of duties involved in the organization, oversight, documentation and compilation of clinical research data. The Clinical Event Classification (CEC) Coordinator II is also responsible for the skills and responsibilities at the CEC CTC I level.

Responsibilities:

• Review CRF to assure compatibility with CEC trial responsibilities
• Depending on trial assignment, may coordinate the work of Clinical Data Assistants working on CEC aspects of the trial
• Use MS Access or other software for purposes of status reporting or communicating trial issues with project team
• Use Clinical Data Management software for tracking, running reports, or viewing CEC related data
• Serve as a mentor to CTC I by welcoming questions, sharing work, delegating progressive responsibility, reviewing their work and providing constructive

coaching and feedback

• Make presentations to project teams and at investigator meetings
• Prepare CEC trial start-up materials
• In collaboration with PL & CEC faculty identify specific adjudication criterion for event classification
• Independently and consistently manage all aspects of CEC operations on multiple small clinical trials, or a large clinical trial

including trials where client is collaborating with other organizations performing parts of the trial CEC process

• Participate in close-out committee decision making regarding (CEC timelines) to trial completion, resolution of unresolved events
• Other duties as assigned
• Full job description available

Education

Completion of RN/PA/Pharmacist training and 2 years healthcare experience; or allied health degree and 5 years healthcare experience; or advanced degree in public health/related field and 1 year clinical trials research experience; or BA/BS and 3 years clinical trials research experience.

About Actalent:

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.