Clinical Research Coordinator I
$22 - $23 per hourSGS
Clinical Research Coordinator IResponsibilities include but are not limited to being lead coordinator on a study, executing follow-up visits ongoing studies, query resolution and other study specific tasks. The CRC I will perform daily tasks such as document review, data entry, test material preparation and data collection. This position may coordinate and execute projects assigned by the Clinic Manager while abiding by Good Clinical Practice (GCP) guidelines.JOB FUNCTIONSPerforms station and instrumentation duties on other studies as assigned, including the collection and recording of clinical informationResponds to queries from Quality Assurance and Statistics departmentsSets up and conducts study in compliance with protocol, SOPs, applicable regulations and GCPsPrepares for and conducts pre-study meetings as well as other meetings and processes as deemed to protocol, SOPs and GCPsMonitor Compliance of panelistsPrepares and is accountable for all Test Material for managed studiesAdheres to study budgetPrepares, completes, organizes and maintains of all study documentation forms, including drafting protocol amendments, case report forms, Electronic Data Capture (EDC), and other study specific documentsAssures that staff working on their managed studies understand and are performing duties according to protocol, SOPs and GCPsCoordinates scheduling subjects for visitsCompletes other duties or tasks assigned by Clinic Manager and/or SupervisorJOB COMPLEXITYMulti-tasking is keyIMPACT OF DECISIONSMake decisions as a study leaderANALYTICAL THINKING/PROBLEM SOLVINGHandle issues with panelists and create solutionsArrange work for studiesQualificationsEDUCATION AND EXPERIENCEAssociate degree or 2 years minimum of relevant work experience with a GED or High School Diploma.Understands basic concepts in clinical research and capable of learning and performing duties during clinical studiesKNOWLEDGE / SKILLS / ABILITIESLanguage SkillsMathematical SkillsReasoning Skills/AbilitiesComputer SkillsAbility to manage and coordinate multiple projects in a fastpaced, highly professional environment.Additional InformationSalary: $22.00 - $23.00/HourOur BenefitsWe care about your total well-being and will support you with the following, subject to your location and role.Health: Medical, dental and vision insurance, life insurance, employee wellness programsWealth: Competitive pay, 401(k) with company match (immediate vesting upon enrollment), employee referral program, annual bonus targetHappiness: Professional Growth: Online training courses, virtual and classroom development experiences, tuition reimbursement programWork-Life Balance: Paid-time off (vacation, sick, company holidays, floating holidays, volunteer time)SGS is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, color, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.To perform this job successfully, an individual must be able to perform each essential duty satisfactorily with or without reasonable accommodations. The requirements listed above are representative of the knowledge, skills, and/or abilities required.This job description should not be construed as an exhaustive statement of duties, responsibilities or requirements, but a general description of the job. Nothing contained herein restricts the company's rights to assign or reassign duties and responsibilities to this job at any time.Job Location
$50k - $52k
Clinical Research Coordinator Title: Clinical Research CoordinatorLocation: Frontage Clinical Services, Inc. in Secaucus, NJReports to: Manager of Clinical OperationsFull-timeFrontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract...SuggestedContract workTemporary workImmediate start$76.86k - $85.88k
...Clinical Research CoordinatorWorks under the supervision of the Principal Investigator (PI), Director and other site personnel as applicable. Conceptually applies the research protocol to the clinical setting to allow accurate and timely completion of all duties. Maintains...SuggestedWork experience placementWork at office- ...Get AI-powered advice on this job and more exclusive features. The Clinical Research Coordinator will oversee the day-to-day operations of clinical trials, ensuring they are conducted ethically and according to protocol. Key Activities Protocol Familiarization : Understanding...SuggestedFull timeContract work
$65k - $80k
...Clinical Research CoordinatorVitalief is a trusted partner to Sponsors, CROs, and Sites across the research and clinical trials landscape... ...patients.We are looking for an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time employee with comprehensive...SuggestedFull timeTemporary workWork at officeLocal areaMonday to Friday$32 - $35 per hour
...Job Title: Clinical Research Coordinator Job Description We are seeking a dedicated Clinical Research Coordinator to join our team. In this role, you will assist in literature reviews, proposal development, and oversee various clinical research activities. You will ensure...SuggestedContract workTemporary work- ...Vitalief, a research-focused consultancy, seeks an Oncology Nurse (RN) to join as a full-time employee at a leading research... ...role includes comprehensive benefits and training in clinical trials. You will coordinate Phase II–IV oncology trials, provide patient-centered care...Full timeMonday to Friday
$30 - $33 per hour
*URGENT NEED - Clinical Research Coordinator Responsibilities + Lead and coordinate the initiation and activation of new clinical trial protocols, ensuring all pre-activation requirements are complete. + Verify approvals from Scientific Review Board (SRB), Institutional...Contract workTemporary work- ...Vitalief is looking for a Senior Clinical Research Coordinator to manage a portfolio of oncology clinical trials in Newark, NJ. The role is full-time and requires at least 3 years of relevant experience to oversee multiple studies, ensuring compliance with protocols and...Full time
$65k - $78k
...Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional... ...SUMMARY: We are seeking an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time employee with...Full timeTemporary workWork at officeRemote work2 days per week3 days per week$65k - $78k
Vitalief Inc. is looking for a Clinical Research Coordinator (CRC) to support a vascular medical device registry study in Newark, NJ. The ideal candidate has at least 2 years of CRC experience, a strong interest in cardiovascular research, and is able to work independently...$65k - $78k
Vitalief is seeking an experienced Clinical Research Coordinator (CRC) to join their team in Newark, NJ. This full‑time position supports a vascular medical device registry study at a community hospital. The ideal candidate will have two years of CRC experience, excellent...Full time2 days per week3 days per week$55k - $60k
...Clinical Research CoordinatorVitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative... ....Vitalief is seeking an experienced Clinical Research Coordinator to join our team as a full-time employee with a comprehensive...Full timeTemporary workWork at officeRemote workMonday to Friday1 day per week$22 - $23 per hour
SGS in Union, New Jersey is looking for a Clinical Research Coordinator to lead and coordinate studies while ensuring compliance with Good Clinical Practice (GCP). The role includes executing daily tasks such as data collection, document review, and scheduling subjects...Hourly pay- Vitalief is seeking an experienced Clinical Research Coordinator to join our team as a full-time employee supporting Phase II-IV oncology interventional trials at a community hospital site in Newark, NJ. This role is ideal for someone with 6-12 months of coordination experience...Full time
- Vitalief is seeking an experienced Clinical Research Coordinator to join our team as a full-time employee supporting Phase II-IV oncology interventional trials at a community hospital site in Newark, NJ. This role focuses on coordinating multiple trials with a collaborative...Full time
- Frontage Laboratories Inc. is seeking a Clinical Research Coordinator in Secaucus, NJ, to support planning, implementation and direction of clinical trials. You will perform study procedures, transcribe data to case report forms, liaise with sponsor personnel, and maintain...
$65k - $80k
Vitalief, located in Rahway, NJ, is seeking a Clinical Research Coordinator to support cardiovascular clinical trials at community hospital sites and outpatient clinics. The ideal candidate will have at least two years of CRC experience, a strong attention to detail, and...$75k - $85k
Position Summary Vitalief is seeking an experienced Senior Clinical Research Coordinator (CRC) to join our team as a full‑time employee. The role supports a portfolio of Phase II-IV oncology interventional clinical trials at a community hospital site in Newark, NJ. Responsibilities...Full timeTemporary workWork at officeRemote workMonday to Friday1 day per week- ...01444 Summarized Purpose: Accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified... ...report form completion and other study-related issues. May coordinate all start-up activities and ensures that timely ethics...Contract workLocal area
- ...biotech experience. Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience with emphasis on Phase II-IV clinical trials. Process and system thinking, customer orientation, and ability...Permanent employment
$130k - $157.5k
...Clinical Trial Manager, Oncology, AsiaEikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the... ...develop and maintain strong relationships with investigators, study coordinators, and study site personnel to facilitate patient recruitment...Summer holidayWork at office3 days per week$55 - $63 per hour
...Clinical Research Nurse The primary purpose of the Clinical Research Nurse is to ensure the successful, patient-oriented, safe, and effective... ...and input data into the clinical trials database. Coordinate patient reimbursement and manage oncology nursing care in collaboration...Contract workTemporary workWork at office- ...Department is responsible for all anatomic and clinical laboratory services at Trinitas... ...Jersey -- whether that be enhancing the coordination for treating complex health conditions... ...high-quality patient care, leading-edge research, and world-class health and medical...Local area
- Internship Position: Clinical Program Coordinator Intern Company: Neuropath Healthcare Solutions Location: Union, New Jersey Duration: 6 Months... ...procedures. Stay informed about current behavioral health trends, research, and best practices for program enhancement. Learn to...TraineeshipWork experience placementInternshipWork at officeMonday to FridayFlexible hoursDay shift
- ...fellowship program. - The Global Clinical Supply (GCS) organization is... ...understanding of drug development, clinical research, and/or clinical supply chain, as well... ...of experience in planning, scheduling, coordination and processing of clinical supply activities...Part timeFor contractorsLocal area
- ...Ventures and Material Impact, the team is moving from pilot execution into the next stages of commercial deployment. The Director of Research & Development is accountable for building and leading Still Bright’s research function and delivering the experimental, technical,...Temporary workLocal areaShift work
$75k
...for faster, more accurate resultsOutpatient & Specialty Care - coordinated care across multiple disciplinesOur HospitalsExplore our... ...Patient Populations:Adults (18-70) and Geriatric (55+)Caseload / Clinical Oversight:Direct clinical oversight and case review are assigned...Work at officeLocal areaMonday to FridayAfternoon shift- Merck & Co. is seeking a senior leader for Global Clinical Trial Operations. You will translate TA objectives into robust operational strategies and guide cross-functional teams to execute HQ-sponsored trials, including regulatory commitments, on time and within budget...
- ...pilot work. Key Responsibilities Run day‑to‑day lab operations: manage equipment, consumables, reagents, and chemical inventory; coordinate vendors and service contracts; and keep the lab organized, well‑stocked, and audit‑ready. Own quality control: manage technician...Full timeLocal areaRemote workRelocation
- Job DescriptionAramark Healthcare+ is seeking an Environmental Services Manager to join our team at Atrium Health Union in Union, NC. The Environmental Services (EVS) Manager is responsible for developing and executing facility solutions to ensure all health and safety ...
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