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 will review documentation, coordinate clinical study project details, and maintain data systems with a sense of urgency aligned with that of our customers. The position involves conducting trial coordinator activities for EmVenio Research’s decentralized network, assessing and following trial participants, and ensuring regulatory compliance for assigned mobile clinics and clinician teams. Additional focus is on timely and accurate EDC data entry and query resolution. Qualifications Bachelor’s degree (B.A. / B.S.) from a four‑year college or university or equivalent combination of education, training, and experience that provides the required knowledge, skills, and abilities Two (2) years research experience strongly preferred; phlebotomy and ECG 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 master all clinical trial database systems Proven ability to coordinate multiple studies while 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 Ability to 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 SOPs, and Working Practice Documents for all non‑clinical/clinical aspects of project implementation, execution, and closeout Ability to complete EmVenio Research clinical training program Ability to perform successfully under pressure while prioritizing multiple projects or activities Strong interpersonal skills to interact with multiple people at many different levels May be responsible for basic clinical assessments Essential Functions / Areas of Accountability Complete study tasks as outlined by trial protocol Ensure documentation is accurate according to EmVenio guidelines and protocols Achieve EmVenio standards for quality, customer service, productivity, and teamwork through participation in risk and quality improvement programs, clinical meetings, and other required meetings Work collaboratively with nurses, physicians, nurse practitioners, physician assistants, clinical research specialists, leaders, family members, key caregivers, and ancillary medical personnel as appropriate Communicate with key stakeholders such as the Principal Investigator, clinical trials team, quality department, and regulatory personnel Perform ECGs, draw blood (phlebotomy), process and ship lab specimens, and other clinical assessments as required Consult with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with guidelines Review the medical and social history of members Assist in building the community research site network and developing relationships within the community Participate in recruitment of participants, including engaging the general public face to face in local and hard‑to‑reach communities, attending community events, speaking with physicians, and supporting enrollment targets Document recruiting efforts and outreach progress Facilitate conversations with potential participants through inbound and outbound calls, sometimes serving as their first introduction to research Participate in all mandatory compliance, patient engagement, and other training programs; seek guidance for compliance‑related concerns and adhere to all applicable laws, regulations, and EmVenio policies Maintain positive control of all PHI information Participate in required training and education programs Ensure adherence to clinical trial protocols and support the clinical trials team in complying with all regulatory, state, national, and international Good Clinical Practice (ICH GCP) guidelines Ensure timely and accurate data collection and completion of case report forms relevant to clinical trials or research projects Assist liaising with monitors of clinical trials and be available for monitoring and audits when required, with full patient documentation available Assist in educating EmVenio Research staff and participants regarding the designated clinical trial, procedures, relevant investigations, and raising the research profile throughout EmVenio Research Perform any other duties needed to help drive EmVenio’s purpose, fulfill our mission, and abide by our core values The typical base pay range for this role is USD $54,080 – $74,880 per year. Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills and other market‑based factors. 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 Please contact Carson Moreira‑Rego at View phone number on click.appcast.io or at Carson.Moreira‑R to learn more about our opportunities where you can make a difference in your own career! Professional Case Management is an Equal Opportunity Employer. #J-18808-Ljbffr Professional Case Management