Part Time Pcm Trials Jobs (NOW HIRING)

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 department, regulatory

Certain assignments may require provider to perform ECGs, draw blood (Phlebotomy), process and ship lab specimen, etc.

Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with guidelines

Reviews the medical and social history of members

Assist in building the community research site network and developing relationships within that community

Participates in recruitment of participants to include personally engaging the general public face to face in local across hard-to-reach communities, attending community events, speaking with physicians and people across diverse cultures and backgrounds to support meeting participant enrollment targets

Documenting recruiting efforts and outreach progress

Facilitates conversations with potential participants through both inbound and outbound calls sometimes serving as their first introduction to research

Participates in all mandatory compliance, patient engagement and other training programs, seeks guidance for compliance-related concerns and adheres to all applicable laws, regulations and EmVenio policies and procedures

Maintains positive control of all PHI information

Participates in required training and education programs

Ensures adherence to clinical trial protocols and supports the clinical trials team in ensuring that trials are conducted and comply with all regulatory, state, national and internationally accepted guidelines for Good Clinical Practice (ICH GCP).

Ensures timely and accurate data collection and completion of case report forms relevant to clinical trials or research projects.

Assists in liaising with monitors of clinical trials and available to monitor and/or audit when required, with full patient documentation available.

Assists in educating EmVenio Research staff and participants regarding the designated clinical trial and procedures and relevant investigations associated with the designated clinical trial and to raise the profile of research throughout the EmVenio Research.

Any other duties needed to help drive EmVenio's purpose, fulfill our mission, and abide by our core values.