We have openings for clinical research coordinators to best match your experience level. Medpace is a full-service clinical contract research organization (CRO). Our clinical operations activities are...

We have openings for clinical research coordinators to best match your experience level. Medpace is a full-service clinical contract research organization (CRO). Our clinical operations activities are...

Contract, 6 months, 100% onsite.Monday-Friday, core daytime business hours based on clinic hours, could have some earlier morning star.

Contract, 6 months, 100% onsite.Monday-Friday, core daytime business hours based on clinic hours, could have some earlier morning star.

The Clinical Research Coordinator 1 assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementat...

The Clinical Research Coordinator 1 assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementat...

Understands basic concepts in clinical research and capable of learning and performing duties during clinical studies. This position may coordinate and execute projects assigned by the Clinic Manager ...

Understands basic concepts in clinical research and capable of learning and performing duties during clinical studies. Responsibilities include but are not limited to being lead coordinator on a study...

Understands basic concepts in clinical research and capable of learning and performing duties during clinical studies. This position may coordinate and execute projects assigned by the Clinic Manager ...

Understands basic concepts in clinical research and capable of learning and performing duties during clinical studies. Responsibilities include but are not limited to being lead coordinator on a study...

While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and pla...

While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and pla...

Joule is currently looking to hire a Clinical Research Coordinator to work in North Dallas. Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible ...

Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements.

Joule is currently looking to hire a Clinical Research Coordinator to work in North Dallas. Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible ...

Supports enrolling patients onto the clinical trial through screening, enrollment and follow up of eligible subjects according to protocol requirements.

Clinical Research Coordinators are responsible to coordinate and manage multiple studies. Clinical Research Coordinators. IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!.

Clinical Research Coordinators are responsible to coordinate and manage multiple studies. Clinical Research Coordinators. IMPROVE THE FUTURE AS OUR CLINICAL RESEARCH COORDINATOR!!!.

We are seeking a full-time  Clinical Research Coordinator  with a minimum of 2-3 year of clinical experience, Ideally would also have Endocrinology experience. ...

While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply...

Clinical Research Coordinators  here at  Revival Research Institute , should be genuinely respectful of diverse points-of-view and strive for an environment in which inclusiveness drive...

While not a requirement, senior pre-medical students who hope to gain experience in clinical research or recent graduates who have a "gap" year before they start medical school are encouraged to apply...

Provides assistance to practice manager, clinical coordinator, mid-level providers, and physicians as related to drug study responsibilities. At least two years experience in a clinical research setti...

Cert Clinical Research Assoc (CCRA), Cert Clinical Research Coord (CCRC), CCRP-Cert Clnl Research Prof (CCRP-RES): Research Certification and/or certification that pertains to particular work area mus...

Provides assistance to practice manager, clinical coordinator, mid-level providers, and physicians as related to drug study responsibilities. At least two years experience in a clinical research setti...

Cert Clinical Research Assoc (CCRA), Cert Clinical Research Coord (CCRC), CCRP-Cert Clnl Research Prof (CCRP-RES): Research Certification and/or certification that pertains to particular work area mus...

Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Collects and ensures quality control of clinical or basic research d...

Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Collects and ensures quality control of clinical or basic research d...

They will work closely with research participants and with other clinical research team members, including CRCs, post-doctoral fellows, members of collaborating research groups, Program Managers, and ...

They will work closely with research participants and with other clinical research team members, including CRCs, post-doctoral fellows, members of collaborating research groups, Program Managers, and ...

Maintain and coordinate data collection information required for each study which may also include developing CRF’s or data collection tools o Assist in developing and implementing research studies to...

Directly interacts with clinical research participants, as required, for the research study. Maintain and coordinate data collection information required for each study which may also include developi...

Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Assists PI/supervisor with daily activities of the research team and...

Directly interacts with clinical research participants, as required, for the research study (non-clinical and clinical procedures). Assists in developing and implementing research studies, may include...

The Clinical Research Coordinator 1 assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementat...

The Clinical Research Coordinator 1 assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementat...

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

The Clinical Research Coordinator may coordinate device and drug treatment research trials, as well as observational studies conducted at Children's Medical Center, including but not limited to study ...

Responsibilities The essential duties and responsibilities: Build templates for clinical trials budgets working in conjunction with practice, third party vendors, and industry contracts Track and moni...