Clinical Research Coordinator

Pcmworkday

Base: $54,080 - $74,880 py; bonus/equity: not spec...
Onsite
Technical and administrative support
Direct patient care
Reviewing documentation
The Clinical Research Coordinator position at PCM involves providing technical and administrative support to clinical operations teams and engaging with research study participants. The role requires strong organizational skills, attention to detail, and the ability to manage multiple tasks efficiently while ensuring compliance with clinical trial protocols

Job Summary

  • As an on-site Clinical Research Coordinator (CRC), you will provide technical and administrative support to your assigned clinical operations team in the field as well as direct patient care of research study participants.
  • The position will involve the conduct of trial coordinator activities for EmVenio Research’ decentralized network, including assessing and following trial participants along with other trial protocol-related activities.
  • Available Benefits Include Medical Dental Vision 401(k) Company Paid Short Term Disability Flexible Spending Account (FSA) Health Savings Account (HSA) Paid Time Off Voluntary Benefits.

Matching Summary

Match Score: 85

The Clinical Research Coordinator position at PCM involves providing technical and administrative support to clinical operations teams and engaging with research study participants. The role requires strong organizational skills, attention to detail, and the ability to manage multiple tasks efficiently while ensuring compliance with clinical trial protocols.

Salary

Base: $54,080 - $74,880 per year; Bonus/Equity: Not specified; Benefits: Medical, Dental, Vision, 401(k), STD, FSA, HSA, PTO, Voluntary Benefits

Skills & Requirements

Must-have

  • Technical and administrative support
  • Direct patient care
  • Reviewing documentation
  • Coordinating clinical study details
  • Maintaining data systems
  • EDC data entry and query resolution

Nice-to-have

  • High attention to detail
  • Sense of urgency
  • Client-focused team
  • Flexibility to reprioritize workload
  • Strong interpersonal skills

Key Requirements

  • Bachelor's degree or equivalent experience
  • Two (2) years research experience
  • ACRP or SOCRA Clinical Research Certification (Preferred)
  • Clinical Research Training Certification (Preferred)
  • Excellent computer skills, proficient in MS Word, Excel, PowerPoint
  • Proven ability to coordinate multiple studies
  • Proven ability to communicate effectively
  • Excellent organizational skills
  • Ability to analyze project specific data/systems
  • Adherence to FDA Good Clinical Practices
  • Ability to complete EmVenio Research clinical training program

Work Rights

Not specified

Tailored Resume

Cover Letter