Clinical Research Coordinator
$65k - $75kRovia Clinical Research
Position Summary The Clinical Research Site Lead is responsible for managing and executing clinical trials in accordance with study protocols, ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success. Key Responsibilities Conducts and coordinates patient visits in accordance with study protocols. Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable. Ensures informed consent is properly obtained and documented. Educates and guides participants through the study, ensuring a positive patient experience. Monitors subject safety, reports adverse events, and escalates concerns as appropriate. Completes timely and accurate source documentation and EDC data entry. Resolves data queries and ensures data integrity. Maintains investigational product accountability and proper storage and handling. Prepares for and supports monitoring visits, audits, and inspections. Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow. Perform other duties as assigned. Skills / Abilities Strong knowledge of medical terminology and clinical procedures. Understanding of ICH/GCP and regulatory requirements. Excellent organizational skills and attention to detail. Strong interpersonal and patient-facing communication skills. Ability to multitask and manage competing priorities in a fast-paced environment. Proficiency in Microsoft Office, EDC, and CTMS applications. Ability to work both independently and collaboratively. High level of professionalism and commitment to patient confidentiality. Education / Experience High school diploma required, bachelor’s degree in related field preferred. 4+ years of clinical research experience. Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred. Pay Range 65,000 - 75,000 USD per year (Ridgeland) #J-18808-Ljbffr
$65k - $75k
...Senior Clinical Research Coordinator Role in Ridgeland, MS (39157) Position Overview The Senior Clinical Research Coordinator/Site Lead is responsible for overseeing the daily execution of clinical trials while ensuring compliance with study protocols, regulatory guidelines...SuggestedPermanent employmentWork at officeMonday to Friday- ...technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site... .... We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily...SuggestedFull timeWork at office
$65k - $75k
...Medix™ is seeking a Senior Clinical Research Coordinator in Ridgeland, MS, to oversee daily clinical trial executions while ensuring compliance with regulatory guidelines and protocols. The position requires strong organizational and communication skills, with a preference...SuggestedMonday to Friday- ...Iterative-Health is hiring a Clinical Research Coordinator in Flowood, MS. This full-time role will involve managing clinical trials, recruiting patients, and ensuring adherence to research protocols. The ideal candidate will have at least 1-2 years of clinical research...SuggestedFull time
- ...technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site... ...therapeutics for patients in need. Senior Clinical Research Coordinator Iterative Health is a healthcare technology and services...SuggestedFull timeWork at office
- ...technology and services company powering the acceleration of clinical research to transform patient outcomes. The Iterative Health Site... ...therapeutics for patients in need. Senior Clinical Research Coordinator Iterative Health is a healthcare technology and services company...Full timeWork at office
- ...Iterative Health in Flowood, MS is seeking a full-time Clinical Research Coordinator to manage industry-sponsored clinical trials. The role involves leading patient recruitment, scheduling visits, and maintaining study documentation. Candidates should have 1-2 years of...Full time
- ...Iterative Scopes is searching for a full-time Clinical Research Coordinator in Flowood, Mississippi. The ideal candidate will manage clinical trials and recruit participants, ensuring adherence to protocols. A preferred background includes a Medical Assistant or higher...Full time
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$50k
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- ...patients. At HCA Healthcare Trident Hospital our nurses set us apart from any other healthcare provider. We are seeking a(an) Clinical Nurse Coordinator Surgical ICU to join our healthcare family. Benefits HCA Healthcare Trident Hospital, offers a total rewards...Hourly payFull timeTemporary workPart timeRelocation packageFlexible hoursShift work
- ...every year, nurses at HCA Healthcare Trident Hospital have the opportunity to make a real impact. As a Behavioral Health Clinical Nurse Coordinator RN you can be a part of change. BenefitsHCA Healthcare Trident Hospital, offers a total rewards package that supports the...Hourly payFull timeTemporary workPart timeFlexible hoursShift work
- Our techs perform immunohematology reference work and consultations for our customer hospitals in a pleasant and low stress environment. In addition to reference work, our techs process samples for outsourced testing; evaluate laboratory data and test results; investigate...
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