Find & Apply For Clinical Research Coordinator / Manager Jobs In Cumberland, Maine
Clinical Research Coordinator/Manager jobs in Cumberland, Maine involve coordinating and managing clinical research studies. Responsibilities include recruiting participants, ensuring compliance with protocols, collecting and analyzing data, and overseeing study operations. Successful candidates typically have a background in healthcare or a related field, along with strong organizational and communication skills. Below you can find different Clinical Research Coordinator/Manager positions in Cumberland, Maine.
Jobs in Cumberland
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.
Latest Jobs in Cumberland
Salary Information & Job Trends In this Region
Clinical Research Coordinators / Managers in Cumberland, Maine play a vital role in overseeing medical research projects and ensuring compliance with regulatory standards. - Entry-level Clinical Research Coordinator salaries range from $40,000 to $55,000 per year - Mid-career Clinical Research Manager salaries range from $55,000 to $75,000 per year - Senior Clinical Research Director salaries range from $75,000 to $100,000 per year The position of Clinical Research Coordinator / Manager has been integral in Cumberland, Maine, particularly due to the region’s focus on healthcare and medical advancements. Historically, these professionals have facilitated numerous clinical trials and medical research initiatives that have contributed significantly to medical science. Over the years, the role of Clinical Research Coordinators / Managers in Cumberland has evolved from merely overseeing clinical trials to also ensuring ethical standards, managing complex regulatory requirements, and implementing technological advancements in data management and trial monitoring. Current trends in the field include an increased emphasis on precision medicine and patient-centric trials, the use of big data and analytics to enhance trial design and outcomes, and stringent regulatory changes that demand more rigorous oversight and reporting in clinical research.
