The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as doc. ...
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 investigator, clinical research coordinator, and clinical team, participates in the review of studies f...
We are looking for a detail-oriented and proactive Studies Coordinator to join our Photoprotection – US Clinical & Instrumental Evaluation Intelligence Team. OTC product testing, or clinical research preferred but not required. Job Description: Studies Coordinator – Photoprotection. Photoprotection ...
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. CRC applies critical thinking and crea...
The Clinical Research Coordinator III will serve as a member of the research team. Rutgers, The State University of New Jersey, is seeking a Clinical Research Coordinator III for the department of Neurosurgery at the Robert Wood Johnson Medical School. This position is responsible for coordinating a...
Duration: 12 Months (Possibility of extension) Job Description:The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operat...
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). The Clinical Research Coordinator will conduct study operations and activities of designated studies, including those that are part of the ...
Required Skills: Minimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance and data management. Job Responsibilities: Under the direct supervision of the N...
PCR CRCNJ seeks a Clinical Research Coordinator who will be responsible for managing the day-to-day operations of assigned clinical trials, assisting in project planning, and ensuring that pre-established work scope, study protocol, and regulatory requirements are followed. The Clinical Research Coo...
As a Clinical Research Nurse, you will play a crucial role in initiating and activating clinical trial protocols, ensuring adherence to regulatory and institutional standards, and providing high-quality patient care. Job Title: Clinical Research Nurse (ONCOLOGY EXP, NEEDED). Your responsibilities in...
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 Practices (GCP), Standard Operating Procedures (SOP), and Federal and applicable regulations. Perfo...
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 compliance, data management, and ensuring Serious Adverse Events (SAEs) are completed and reported within rep...
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 Practices (GCP), Standard Operating Procedures (SOP), and Federal and applicable regulations. Perfo...
The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as documenting and reporting on the daily operations of assigned trials. CRC applies critical thinking and crea...
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forens...
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 investigator, clinical research coordinator, and clinical team, participates in the review of studies f...
The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forens...
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 research experience*. ...
Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consen...
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 research experience*. ...
Assist in the conduct of clinical trials as specified by the study protocol under the supervision of designated Principal Investigator and departmental management. ...
Assist in the conduct of clinical trials as specified by the study protocol under the supervision of designated Principal Investigator and departmental management. ...
Occasionally attending out-of-town Investigator Meetings Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent Facilitate ef...