Responsible for coordinating and performing study specific clinical and regulatory activities across multiple study protocols of different therapeutic areas and phases, in accordance with appropriate ...

Responsible for coordinating and performing study specific clinical and regulatory activities across multiple study protocols of different therapeutic areas and phases, in accordance with appropriate ...

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

Knowledge of clinical research coordinator duties. Collaborate with the clinical research team to ensure timely prescreening of potential subjects and active cancer patients for all available clinical...

Coordinates the development of forms, questionnaires and the application of research techniques, assists in writing procedure manuals, reviews journals, abstracts and scientific literature to keep abr...

Knowledge of clinical research coordinator duties. The Research Nurse Clinician assists investigators in preparing and implementing new clinical trials, screens and enrolls study participants, and pro...

Clinical Research Coordinator, you will be responsible for coordinating and facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical...

Knowledge of clinical research coordinator duties. The Research Nurse Clinician assists investigators in preparing and implementing new clinical trials, screens and enrolls study participants, and pro...

Association of Clinical Research Professional as a Clinical Research Analyst (CRA) or Society of Clinical Research Associates (SoCRA) certification as a Clinical Research Professional (CCRP) preferred...

Responsible for coordinating and performing study specific clinical and regulatory activities across multiple study protocols of different therapeutic areas and phases, in accordance with appropriate ...

Responsible for coordinating and performing study specific clinical and regulatory activities across multiple study protocols of different therapeutic areas and phases, in accordance with appropriate ...

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...

Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...

Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...

The primary purpose of the Clinical Research Coordinator II (CRCII) position is to assist the research team with day-to-day operations related to protocol start up, implementation and follow up of epi...

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal inv...

Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...

Experience in clinical research, clinical operations, or billing compliance.

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...

Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. PR...

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal inv...

Coordinates the synchronization of research activities within the ARJR service under the direction of the ARJR Director and serves as a liaison between the clinicians, research staff, and other resear...

Minimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory complianc...

Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...

Reports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...

SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Along with clinical research nurses, ma...

Minimum of three years in a Study Coordinator or Clinical Research Coordinator role. Oncology Clinical Research Coordinator. This is a contract position and requires previous Oncology clinical researc...

Minimum of three years in a Study Coordinator or Clinical Research Coordinator role. Oncology Clinical Research Coordinator. This is a contract position and requires previous Oncology clinical researc...

Coordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and st...

Coordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and st...

The Laboratory Coordinator plays a crucial role in the execution of clinical lab testing protocols, and new assay and new instruments validation and verification. The individual will assist to perform...

Position Summary Working in the Division of General Medicine under the direction of the Principal Investigator, the Coordinator will provide coordination and data collection in NIH-sponsored research ...

Position Summary Working in the Division of General Medicine under the direction of the Principal Investigator, the Coordinator will provide coordination and data collection in NIH-sponsored research ...