Find & Apply For Clinical Research Coordinator Jobs In Kennebec, Maine
Clinical Research Coordinator jobs in Kennebec, Maine involve coordinating and overseeing clinical research studies. Responsibilities include managing research protocols, recruiting participants, collecting data, and ensuring compliance with regulations. These positions require strong organizational and communication skills, as well as attention to detail. Below you can find different Clinical Research Coordinator positions in Kennebec, Maine.
Jobs in Kennebec
Browse jobs from a variety of sources below, sorted with the most recently published, nearest to the top. Click the title to view more information and apply online.
Clinical Research Project Coordinator I-II
Intermountain Health
Kennebec, ME
Dispute Resolution Reviewer III
St George Tanaq Corporation
Kennebec, ME
Senior In-House CRA (Remote – Continental US)
United Therapeutics Corporation
Kennebec, ME
Latest Jobs in Kennebec
Salary Information & Job Trends In this Region
Clinical Research Coordinators in Kennebec, Maine play a crucial role in coordinating and overseeing clinical research studies in various healthcare settings. - Entry-level Clinical Research Coordinator salaries range from $35,000 to $45,000 per year - Mid-career Clinical Research Coordinator salaries range from $45,000 to $60,000 per year - Senior Clinical Research Coordinator salaries range from $60,000 to $85,000 per year The history of Clinical Research Coordinators in Kennebec, Maine dates back to the early days of clinical trials when researchers began to standardize protocols and procedures for conducting studies. As the field of clinical research has evolved, Clinical Research Coordinators in Kennebec, Maine have become more specialized in areas such as oncology, cardiology, and neurology, working closely with research teams to ensure the successful implementation of studies. Current trends in the field of Clinical Research Coordinators in Kennebec, Maine include the use of electronic data capture systems, remote monitoring of study participants, and an increased focus on patient-centered care and informed consent processes. These professionals play a vital role in advancing medical knowledge and improving patient outcomes through their dedication to the ethical and efficient conduct of clinical research studies.