Clinical Research Coordinator
Vitalief
Vitalief, a research-focused consultancy, seeks an Oncology Nurse (RN) to join as a full-time employee at a leading research center in Livingston, NJ. The role includes comprehensive benefits and training in clinical trials. You will coordinate Phase II–IV oncology trials, provide patient-centered care, collaborate with multidisciplinary teams, and utilize OnCore CTMS, EPIC, and related systems. Schedule is 8:00 AM–4:30 PM, Monday to Friday, on site. #J-18808-Ljbffr
$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...SuggestedContract workTemporary work$25 per hour
...Job Description Job Description Job Title: Clinical Research Coordinator (LT) Job Description The Clinical Research Coordinator (LT) supports the successful initiation, activation, and ongoing management of oncology clinical trials across multiple disease-specific...SuggestedFull timeContract workTemporary workWork at office$22 - $23 per hour
...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...SuggestedWork experience placementImmediate start- ...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- ...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$55 - $63 per hour
...Job Description Job Description Job Title: Clinical Research Nurse Job Description The primary purpose of the Clinical Research Nurse... ...and input data into the clinical trials database. Coordinate patient reimbursement and manage oncology nursing care in collaboration...Contract workTemporary workWork at office- 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
$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- ...of activities provided by external contract laboratoreis both clinical and pre clinical. Ensures all necessary documentation is inmplace... ...responsibilities include reviewing/distributing all external research reports.Additional InformationRegards,Anuj Mehta(***) ***-****SummaryType...Contract workImmediate start
- AbbVie in New Jersey seeks a Medical Director/Scientific Director to oversee clinical trials within a development program. You will supervise study design, data interpretation, and cross-functional collaboration to deliver high-quality clinical data supporting product...
$72.8k - $87.36k
...Clinical Research Coordinator – Wichita, KS Work Set-Up: On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward...Hourly payFull timePart timeImmediate startWorldwide$55k - $77k
...A leading pharmaceutical company is seeking a Marketing Coordinator to drive the execution of multi-channel digital campaigns. This role involves managing paid media, CRM, social, and web activation programs, ensuring alignment with brand standards. The ideal candidate...$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- IQVIA is seeking a sponsor-dedicated Local Trial Manager to provide country-level oversight of clinical trials from start-up to closeout. The role requires expertise in informed consent, site selection, patient recruitment strategies, and monitoring visit reports, with...Remote jobLocal area
- Atlantic Health Morristown Medical Center in Morristown, NJ, is seeking a Clinical Research Nurse Coordinator for full-time days (8 AM-4 PM). The role coordinates and performs study-specific clinical and regulatory activities across multiple protocols under SOPs and study...Full time
- ...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
$95k - $135k
...best leaders are those who create an inspiring vision for the future and empowers their team to achieve success.The Sr. Manager, Clinical Services functions to varying degrees to achieve the best quality outcomes, patient safety and support to improve patient centered...Minimum wage- ...client advocate. Maintain a comprehensive understanding of your dedicated client’s group health portfolio and other ADP services and coordinate communication among various business partners.Act as a liaison between clients and ADP, collaborating with other ADP partners...Work at office3 days per week
- 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...
- ...Description:Responsible for operational aspects of one or more clinical trials (phase I-IV, Expanded Access, Investigator Initiated, registries... ...specifications. Responsible for management of Contract Research Organizations (CROs) and ensure adherence to scope of work within...Contract workWork at officeLocal areaImmediate start
$125k - $140k
As a Health and Benefits Director, you will be a leader on the client service team and will be responsible for fostering relationships cross the client organization. You will be responsible for managing a wide array of projects, leveraging your experience to make recommendations...Temporary workWork at officeLocal areaVisa sponsorshipWork visaFlexible hours- ...and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description1. Support individual clinical trial teams (CTTs) and Biomarker Sub-teams as required for all technical and operational biosample-related matters for assigned projects...Work at officeImmediate start
$230k - $280k
...play an integral role in supporting the Medical Affairs team, as well as appropriate cross‑functional initiatives such as providing clinical and disease state expertise and product (compound) knowledge to support evidence generation. The Medical Director will serve on...Full timeWork at officeLocal areaImmediate startFlexible hours2 days per week3 days per week
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