Assists in the conduct of clinical trial activities in accordance with applicable regulations
Oversees the conduct of their assigned site and responsible for training of staff/providers
Accountable for enrollment success at sites across all studies
Develops and implements patient recruitment strategies and actively recruits to ensure enrollment targets are achieved
Maintains significant depth of knowledge in coordinating across multiple therapeutic areas
Conducts 1:1 meetings and annual reviews with site staff
Completes all protocol related training
Performs quality control checks on source documentation and regulatory
Works closely with Quality Assurance Department to ensure quality at site
Coordinates protocol related research procedures, study visits, and follow-up
Attends training(s) on leadership, communication, and other topics for management of teams

Requirements

Must have clinical skills experience with patients to obtain vitals and perform procedures such as blood draws, EKG, etc.
Must demonstrate the ability to fulfill responsibilities of CRC Level II
Extensive knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Superior knowledge and experience of site operations and the drug development process
Trained in leadership, project management and process development

Benefits

health insurance
retirement plans
professional development opportunities

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills

clinical skillspatient recruitment strategiesblood drawsEKGGCPICHsite operationsdrug development processquality controlprotocol related training

Soft skills

leadershipcommunicationproject managementteam managementorganizational skillsinterpersonal skillstrainingannual reviewsresponsibility fulfillmentstaff training

Certifications

CRC Level II