Clinical research specialist Jobs in Savannah, GA
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Clinical research specialist • savannah ga
Last updated: 22 hours ago
The Clinical Research Coordinator II (CRC-II) RN is responsible for the coordination of all day-to-day clinical research activities with minimal supervision.
The CRC-II RN is assigned more complex s...Show moreLast updated: 3 days ago
Requisition Number : CLINI002554.Location : Savannah, GA 31405, USA.Pay or shift range : $59,000 USD to $73,000 USD.The estimated range is the budgeted amount for this position.Final offers are based ...Show moreLast updated: 30+ days ago
A company is looking for a Clinical Research Associate - Remote, US based.Key Responsibilities Design, plan, and conduct real-world studies evaluating products and medical devices Coordinate mar...Show moreLast updated: 3 days ago
Maximus is a global organisation that specialises in providing health and employment services to millions of people every year.
Here in the UK we employ around 5,000 people across the country to del...Show moreLast updated: 5 days ago
We are committed to bringing better access to better solutions – and a better life for those living with diabetes – with the world's first bionic pancreas called the iLet.The iLet Bionic Pancreas i...Show moreLast updated: 30+ days ago
Lead clinical operations for a growing early-intervention clinic serving children ages 2–11.Ensure high-quality, ethical service delivery.
Oversee approximately 3 BCBAs and support additional ...Show moreLast updated: 5 days ago
Savannah State University established in 1890, is the first public historically black college or university in the state of Georgia and the first institution of higher learning in the city of Savan...Show moreLast updated: 6 days ago
Clinical Research Coordinator II.The Clinical Research Coordinator II (CRC-II) is responsible for the coordination of all day-to-day clinical research activities with minimal supervision.The CRC-II...Show moreLast updated: 11 days ago
BD is one of the largest global medical technology companies in the world.Advancing the world of health™ is our Purpose, and it’s no small feat.
It takes the imagination and passion of all of us—fro...Show moreLast updated: 30+ days ago
Psychologist (PhD / PsyD) - (Contract / 1099 / Independent Contractor).We are seeking a dedicated and compassionate.PhD or PsyD) to join our team in providing military veterans with thorough mental healt...Show moreLast updated: 4 days ago
Savannah GA 31405 (In-person role).Partial Hospitalization (PHP) Intensive Outpatient (IOP) and Outpatient Detox (OP DTX).
This full-time position involves both.LPC-S LCSW LMFT) who demonstrates.Pro...Show moreLast updated: 4 days ago
Experience the Matrix Providers Advantage.We strive to provide a framework of stability and structure for our valued employees, where you will experience lower provider-to-patient ratios and fair, ...Show moreLast updated: 6 days ago
We are seeking a dedicated and compassionate.PhD or PsyD) to join our team in providing military veterans with thorough mental health compensation and pension exams for service connected issues and...Show moreLast updated: 5 days ago
The Clinical Specialist supports BD's Urology & Critical Care (UCC) portfolio across federal healthcare markets, specifically the Department of Veterans Affairs (VA) and the Department of Defense (...Show moreLast updated: 20 days ago
The Clinical Specialist supports BD’s Urology & Critical Care (UCC) portfolio across federal healthcare markets, specifically the Department of Veterans Affairs (VA) and the Department of Defense (...Show moreLast updated: 19 days ago
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials.Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the co...Show moreLast updated: 6 days ago
Clinical Pharmacist BMT (Bone Marrow / Blood and Marrow Transplant).Full-Time – Days – Rotating Weekends.Our Facility is a state-of-the-art, full-service medical facility located in the heart of nor...Show moreLast updated: 6 days ago
Position Summary •Under the general direction of the Center for Medication Management(s) Manager, provides ambulatory clinical pharmacy care promoting the safe and effective use of drug therapy, acc...Show moreLast updated: 9 days ago
Provides analyst support for claims research activities including reviewing and researching claims to ensure regulatory requirements are appropriately applied, identifying root-cause of processing ...Show moreLast updated: 22 hours ago
Clinical Research Coordinator II - RN
St. Joseph's / CandlerSavannah, GAPart-time
- Promoted
Clinical Director
Youth Advocate Programs, Inc.Savannah, GA, USFull-time
- Promoted
Clinical Research Associate
VirtualVocationsSavannah, Georgia, United StatesFull-time
- Promoted
Clinical Informatician
MAXIMUSSavannah, GA, United StatesFull-time
Clinical Diabetes Specialist - Savannah, GA
Beta Bionics, Inc.Savannah, Georgia, United StatesFull-time
Clinical Director
Pair ABASavannah, GA, USFull-time
- Promoted
Technology Research Technician
Savannah State UniversitySavannah, GA, United StatesFull-time
Clinical Research Coordinator II
St. Josephs CandlerSavannah, Georgia, United States, 31405Full-time
Clinical Specialist – Government Accounts - East Region
BDSavannah,Georgia,USAFull-time
- Promoted
Clinical Psychologist
The Locums Company LLCSavannah, GA, United StatesPart-time
Clinical Director
VSV WINS INCSavannah, Georgia, USAFull-time
- Promoted
Clinical Psychologist
Matrix ProvidersSavannah, GA, United StatesFull-time
Clinical Psychologist
The Locums CompanySavannah, GA, USPart-time
- Promoted
Clinical Specialist - Government Accounts - East Region
Becton, Dickinson and CompanySavannah, GA, United StatesFull-time
- Promoted
Clinical Specialist - Government Accounts - East Region
Becton Dickinson & CompanySavannah, GA, United StatesFull-time
- Promoted
Research Assistant
CenExelSavannah, GA, United StatesFull-time
- Promoted
Clinical Pharmacist
HealthTrust Workforce SolutionsSavannah, GA, USFull-time
- Promoted
Clinical Pharmacy Specialist
St Joseph'S / CandlerSavannah, GA, United StatesFull-time
- Promoted
- New!
Analyst, Claims Research
Molina HealthcareSavannah, GA, USFull-time
- hospital (from $ 36,130 to $ 285,000 year)
- associate dentist (from $ 145,600 to $ 220,000 year)
- owner operator (from $ 100,000 to $ 204,000 year)
- light industrial (from $ 95,000 to $ 200,000 year)
- journeyman lineman (from $ 73,569 to $ 199,875 year)
- pipe welder (from $ 54,600 to $ 195,000 year)
- cyber security (from $ 150,000 to $ 190,000 year)
- mental health (from $ 56,972 to $ 179,920 year)
- mental health therapist (from $ 69,229 to $ 178,328 year)
- Chicago, IL (from $ 62,719 to $ 109,500 year)
- Los Angeles, CA (from $ 65,676 to $ 105,750 year)
- Philadelphia, PA (from $ 60,912 to $ 84,600 year)
- Santa Maria, CA (from $ 75,500 to $ 82,000 year)
- Overland Park, KS (from $ 62,920 to $ 77,000 year)
- North Charleston, SC (from $ 47,920 to $ 69,713 year)
- Phoenix, AZ (from $ 54,824 to $ 69,225 year)
- Charleston, SC (from $ 47,840 to $ 67,600 year)
The average salary range is between $ 53,625 and $ 90,000 year , with the average salary hovering around $ 69,688 year .
Clinical Research Coordinator II - RN
St. Joseph's / CandlerSavannah, GA3 days ago
Job type
- Part-time
Job description3 Years Nursing experience - Required 1-2 years Clinical Research experience or 2-3 Years Oncology experience - Preferred Professional License with State of Practice - Required CCRC or OCN certification required within 18 months of hire or upon eligibility. Basic Life Support (BLS) - Required Adherence to Ethical Standards : Promotes ongoing compliance with the key ethical concepts of research, including respect for individuals, beneficence, and justice. Adheres to federal and institutional regulations and policies & procedures related to clinical research. Maintains awareness of what constitutes research misconduct and adheres to federal and institutional requirements for reporting research misconduct. Protocol Compliance : Communicates with the interdisciplinary team to ensure protocol compliance and timeliness of protocol-related procedures. Contributes to discussions regarding feasibility of protocol implementation with a specific focus on clinical issues, available resources, study coordination, patient safety, and data quality. Identifies facilitators and barriers to protocol compliance. Promptly reports instances of protocol noncompliance and assists with writing corrective and preventative action plans. Maintains assigned study folders ensuring the use of the current version of the IRB approved protocol, informed consent document, HIPAA authorization form and any other study manuals. Promptly reviews signs-off, and files all essential documents. Informed Consent : Ensures that the most current version of the IRB approved protocol consent document and HIPAA authorization document is used when consenting a patient. Collaborates with the principal investigator to ensure initial and ongoing consent process is performed and documented. Assesses patient’s understanding of the information provided during the informed consent process. Ensures timely reconsent is obtained as necessary. Participant Recruitment & Retention : Identify, screen and enroll participants to clinical trials per established goals. Collaborates with the treating investigator to ascertain study participant eligibility for a clinical trial, ensuring there is documentation to support participant eligibility. Adheres to protocol and coordinates patient care systematically and within the parameters of the research study. Works with individual patients to address barriers to recruitment and retention. Develops relationships and maintains rapport with referring providers, clinical staff, and ancillary departments to facilitate compliance with the research study. Management of Clinical Trial Participants : Educates the patient and family regarding clinical trial participation, clinical condition, and / or disease process. Coordinates, schedules, and ensures timely completion of protocol-required events or other requirements. Evaluates patient’s adherence to and documentation of self-administered study agents and the return of such agents. Adherence to protocol-specific intervention(s), including general indicators, mechanisms of action, and toxicity considerations of treatment modalities (., surgery, antineoplastic medication therapy, radiation therapy, complementary and alternative therapies, cellular therapies). Is knowledgeable regarding protocol-specific maximum tolerated dose and protocol-specific dose-limiting toxicities. Adherence with protocol-specific protective measures for patients who are immunocompromised during the clinical trials (., protocol allowed treatments or interventions). Documentation and Document Management : Documents all participant encounters in the medical record and / or research record. Collects all supporting data including outside medical records and lab reports. Assesses documentation for discrepancies and ensures that inaccurate or discrepant documentation is addressed in the medical record or other source documents. Maintains the privacy and confidentiality of research participant’s source documents. Maintains essential documents per Good Clinical Practice. Utilizes departmental forms to document all required datapoints. Documentation and Document Management : . Documents all participant encounters in the medical record and / or research record. Collects all supporting data, including outside medical records and lab reports. Assesses documentation for discrepancies and ensures that inaccurate or discrepant documentation is addressed in the medical record or other source documents. Maintains the privacy and confidentiality of research participants’ source documents. Maintains essential documents per Good Clinical Practice. Utilizes departmental forms to document all required data points. Data Management : Adheres to study requirements for reporting research data. Ensures that relevant data from source documents are abstracted and reported in an accurate and timely manner and that all data reported can be verified within the source documents. Resolves queries promptly. Assists with the reporting of Serious Adverse Events (SAE) in accordance with the research protocol and reports follow-up safety data upon resolution of the SAE.
Position Summary
The Clinical Research Coordinator II (CRC-II) RN is responsible for the coordination of all day-to-day clinical research activities with minimal supervision. The CRC-II RN is assigned more complex studies, including but not limited to Phase II and Phase III therapeutic clinical trials for various types or stages of cancer. The CRC-II RN is responsible for coordinating multiple clinical trials simultaneously, ensuring full compliance with each research protocol, adhering to applicable federal regulations, Good Clinical Practice (GCP), SJ / C Policies & Procedures, and Institutional Review Board (IRB) requirements. The CRC-II RN works with clinical investigators to recruit diverse research participants representative of the site’s catchment area. Key tasks of the CRC-II RN include but are not limited to the following : obtaining informed consent, confirming participant eligibility, coordinating participant schedules to comply with research protocol requirements, and ensuring the participant’s overall care is coordinated per the parameters outlined in the research protocol. The CRC-II RN also collects and processes blood or other biospecimens, performs EKGs or other clinical assessments as required by the research study, and collects & reports participant data. The CRC-II RN will participate in the review of prospective clinical research studies and take the lead as the primary contact for study selection activities. The CRC-II RN maintains open communication with the other members of the research team and demonstrates the ability to function autonomously and as part of a team.
Education
- Associate's in Nursing - Required
- Bachelor's of Science in Nursing - Preferred
Experience
License & Certification
Core Job Functions