Clinical Research Coordinator (Part-Time)

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’s 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. Qualifications Bachelor's degree (B. A. / B. S.) from a four‑year college or university or an equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities Two (2) years of research experience strongly preferred; phlebotomy and ECGs experience not required but preferred ACRP or SOCRA Clinical Research Certification (Preferred) and Clinical Research Training Certification (Preferred) Excellent computer skills, proficient in MS Word, Excel, PowerPoint, and the ability to obtain knowledge and master all clinical trial database systems Proven ability to successfully coordinate multiple studies while adhering to regulatory and institutional guidelines Proven ability to communicate effectively within an interdisciplinary team to ensure safe, efficient, high‑quality patient care, both in‑person and virtually Excellent organizational skills and strong attention to detail, with a proven ability to handle multiple tasks efficiently and effectively Ability to effectively analyze project‑specific data and 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 the 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 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 Certain assignments may require performing ECGs, drawing blood (phlebotomy), processing and shipping lab specimens, etc. 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 that community Participate in recruitment of participants, personally engaging the general public face‑to‑face in local hard‑to‑reach communities, attending community events, speaking with physicians, and people across diverse cultures and backgrounds to support 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 and procedures 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 ensuring trials are conducted and comply with all regulatory, state, national, and internationally accepted guidelines for Good Clinical Practice (ICH GCP) Ensure timely and accurate data collection and completion of case report forms relevant to clinical trials or research projects Assist in liaising with monitors of clinical trials and be available to monitor and/or audit when required, with full patient documentation available Assist in educating EmVenio Research staff and participants regarding the designated clinical trial, procedures, and relevant investigations associated with the trial and raise the profile of research throughout EmVenio Research 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 $28,080–$38,480 per year. Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of the role, job duties and 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‑View email address on click.appcast.io today 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