Clinical Research Coordinator

Put your talents to work at PCM! Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients. Be a part of our dynamic client-focused team and make a difference in your career!

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. You work with a high attention to detail, reviewing documentation, coordinating clinical study project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers.

The position will involve the conduct of trial coordinator activities for EmVenio Research’ decentralized network. This will include assessing and following trial participants along with other trial protocol-related activities. In this role the CRC is accountable for the regulatory compliance and performance of assigned mobile clinics and clinician teams conducting decentralized trials as well as patient engagement, and screening. Additional focus will be on timely and accurate EDC data entry and query resolution.

Bachelor's degree (B.

A. /

B. S.) from four-year college or university or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities

Two (2) years research experience strongly preferred. Phlebotomy and ECGs experience not required, but preferred.

ACRP or SOCRA Clinical Research Certification (Preferred), Clinical Research Training Certification (Preferred)

Excellent computer skills, proficient in MS Word, Excel, PowerPoint and ability to obtain knowledge and master all clinical trial database systems.

Proven ability to successfully coordinate multiple studies adhering to regulatory and institutional guidelines.

Proven ability to communicate effectively within an interdisciplinary team to ensure safe, efficient, quality patient care, both in-person and virtually.

Excellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively.

Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency.

Flexibility to reprioritize workload to meet changing project timelines.

Responsible for adhering to FDA Good Clinical Practices, FDA regulations, EmVenio Research/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout.

Ability to successfully complete EmVenio Research clinical training program.

Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

Must have strong interpersonal skills to be able to interact with multiple people on many different levels.

May be responsible for basic clinical assessments.

Complete study tasks as outlined by trial protocol

Ensures documentation is accurate according to EmVenio guidelines and protocols is required

Achieves EmVenio standards for quality, customer service, productivity and teamwork through participation in Risk and Quality Improvement programs, clinical meetings and other meetings as required

Works collaboratively with nurses, physicians, nurse practitioners, physician assistants, clinical research specialists, leaders, family members, key care givers and any ancillary medical personnel as appropriate

Communicates with key stakeholders such as the Principal Investigator, clinical trials team and quality…