Clinical Research Coordinator II: TB Trials & Data
Rutgers University
Rutgers University in Newark is seeking a Clinical Research Coordinator II for the Department of Medicine within NJMS. The role involves managing multiple tuberculosis research studies, overseeing protocols, analyzing data, and collaborating with staff to improve patient outcomes. Qualified candidates will have a Bachelor's degree and two years of clinical research experience, focusing on patient recruitment and trial management. The position offers competitive medical and educational benefits. #J-18808-Ljbffr Rutgers University
- ...Position Details Recruitment/Posting Title: Clinical Research Coordinator II Job Category: Staff & Executive -... ...completing documentation, analyzing data, and preparing reports. This is an... ...responsible for managing 4 to 5 concurrent trials. Versatility, a positive "can do"...DataFull timeSeasonal workWork at officeFlexible hoursShift work
$130k - $142.5k
...experienced, and highly motivated Clinical Trial Manager (CTM) to join our... ...high‑quality study data, on time and on budget. Develop... ...relationships with investigators, study coordinators, and study site personnel to... ..., specific to oncology research. Demonstrated experience in...DataSummer holidayWork at office3 days per week- ...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 to work in multidisciplinary...SuggestedPermanent employment
- ...Position: Clinical Research Coordinator III Location: Jersey City, NJ Job Id: 1137 # of Openings: 1 Clinical... ...and to provide the best quality data to the sponsor. To ensure study enrollment... ...standards with all the relevant clinical trial documentation. Completing and...Data
$22 - $23 per hour
...are not limited to being lead coordinator on a study, executing follow‑... ...such as document review, data entry, test material preparation... ...execute projects assigned by the Clinic Manager while abiding by Good... ...basic concepts in clinical research and capable of learning and...DataHourly payWork experience placementImmediate start$65k - $80k
...Sponsors, CROs, and Sites across the research and clinical trials landscape. By blending deep subject matter... ...for an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time... ..., document, and maintain study data in source documents and electronic systems...DataFull timeTemporary workWork at officeLocal areaMonday to Friday- ...Clinical Research Coordinator - Somerset, NJ IQVIA is a global leader in advanced analytics, technology... ...edge technology, we deliver high-quality data and insights that accelerate... ...the successful execution of clinical trials, combining hands-on clinical procedures...DataWorldwide
$60k - $70k
...Sponsors, CROs, and Sites across the research and clinical trials landscape. By blending deep subject matter... ...for an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time... ..., document, and maintain study data in source documents and electronic systems...DataFull timeTemporary workWork at officeMonday to Friday$30 - $33 per hour
...Clinical Research Coordinator Oncology This role leads the initiation and activation of new oncology clinical trial protocols and coordinates day-to-day study operations across multiple sites... ...Oversight Committee (HROC), data collection plans, and finance/contract...DataContract workTemporary work- Allergan is looking for a key member to join its Data Science team as a proactive operational lead for clinical studies. You will align teams with overall strategies... ...successful delivery by managing a clinical trial from initiation to completion. The role requires a...Data
$31 per hour
...for a vacancy for a Paralegal II. In this role, you will be supporting... ..., searches within various data and document sets, analysis... ...in preparation for charging or trial. Reviews, summarizes, and... ...preparation for charging or trial. Researches, analyzes, and summarizes...DataHourly payFull timeTemporary workWork at officeLocal areaRemote work$35 - $42 per hour
IQVIA in Linden, New Jersey is looking for a Clinical Research Coordinator to support clinical studies. The role involves conducting clinical procedures, interacting with patients, and ensuring compliance with protocols. The ideal candidate has clinical research experience...Hourly payFull time$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... ...(GCP). The role includes executing daily tasks such as data collection, document review, and scheduling subjects for visits...DataHourly pay- ...Clinical Project Manager Overall responsibility for overseeing and executing on deliverables for assigned clinical trials. Preparing, overseeing, and reviewing documents pertaining to assigned... ...successful delivery of high quality data that meets timelines while...Data
- ...Technologies Inc is looking for DevOps Engineer- Level II role for one of our premier clients. Job Title : DevOps... ..., rollback, and release validation workflows. Coordinate sandbox refresh schedules and data seeding processes. Automate deployment approvals through...DataFull timeContract workWork at officeWork from homeFlexible hours
$32 - $50.73 per hour
Job Description Medical Laboratory Scientist II - Paterson, NJ, Monday to Friday, 10:30 PM to 7:00 AM, with rotational weekends.... ...dates. Perform and document QC analysis to ensure accuracy of clinical data and proper instrument function. Make quality control decisions...DataHourly payFull timeWork experience placementWork at officeMonday to FridayFlexible hoursShift workWeekend workAfternoon shift$32 - $50.73 per hour
Job Description Medical Laboratory Scientist II - Paterson, NJ - Monday to Friday, 3:00 PM to 11:30 PM, with rotational weekends... ...dates. Perform and document QC analysis to ensure accuracy of clinical data and proper instrument function; make quality control decisions...DataHourly payFull timeWork experience placementWork at officeLocal areaMonday to FridayFlexible hoursShift workWeekend workAfternoon shift$32 - $50.73 per hour
Medical Laboratory Scientist II - Paterson, NJ - Monday to Friday, 3:00 PM to 11:30... ...document QC analysis to ensure accuracy of clinical data and proper instrument function. Make... ...evaluation from IERF (International Education Research Foundation). U.S.‑educated candidates...DataHourly payFull timeWork experience placementWork at officeLocal areaMonday to FridayFlexible hoursShift workWeekend workAfternoon shift$30 - $33 per hour
...Description Job Description Job Title: Clinical Research Coordinator – Oncology Job Description This... ...activation of new oncology clinical trial protocols and coordinates day-to-day... ...Research Oversight Committee (HROC), data collection plans, and finance/contract...DataContract workTemporary work$25 per hour
...Description Job Description Assistant Clinical Research Coordinator Title: Assistant Clinical Research... ...core laboratory services for clinical trials. Position/Job Summary: The... ...and Sub-Investigators. Records study data in the source documents. Evaluates and...DataHourly payFull timeContract workTemporary workImmediate start$75.6k - $106.78k
...RWJBarnabas Health is seeking a Data Engineer II to provide expertise in Epic Cosmos and data engineering. Located in West Orange, NJ, this full-time salaried position offers a salary range of $75,597 to $106,780 annually. The ideal candidate will have a Bachelor's degree...DataFull time- ...fellowship program. The Global Clinical Supply (GCS) organization is... ...full portfolio of clinical trials. GCS supports more than 300 Phase... ...in planning, scheduling, coordination and processing of clinical supply... ...reports. Familiarity with data analytics/visualization software...DataFor contractorsLocal area
$19.76 - $30.33 per hour
...Legal Administrative Assistant II provides administrative and... ...entering and managing case‑related data, including pleadings, motions,... ...and correspondence related to trial, arbitration, and mediation.... ...Manage calendars and coordinate scheduling for hearings, depositions...DataHourly payContract workWork at officeLocal areaWork from homeWork visa- Rutgers University is seeking a Research Support Associate for the Department of Health Informatics. The role involves supporting NIH clinical trials, preparing research documents, and recruiting participants. Candidates should have a Bachelor's degree in a health-related...Data
- Quest Diagnostics Incorporated is seeking a Phlebotomist II for a part-time position in Belleville, NJ. The role involves collecting... ...in accordance with established procedures, ensuring accuracy in data entry and adhering to corporate policies. Qualified candidates must...DataHourly payPart timeFlexible hours
- McKinsey & Company in Newark is seeking a Data Engineer II who will design and optimize modern data platforms that enable advanced analytics and AI solutions. You'll collaborate with interdisciplinary teams to build scalable pipelines and manage secure data environments...Data
- ...Job Description Title: Phlebotomist II Location: Bloomfield NJ 07003 Duration... ...with confidence, both the forensic and clinical specimen collection and processing duties... ...service environment preferred. ~ Keyboard/data entry experience Meet Your...DataWork experience placementWork at officeFlexible hoursShift work
$19.41 - $29.12 per hour
...Phlebotomist II Part-Time - Belleville, NJ, Monday to Friday, 9:00 AM to 1:00 PM, with... ...solutions according to established training. Research test/client information and confirm and... ...navigate a computer and accurately enter data is a requirement to be successful in this...DataPart timeWork experience placementMonday to FridayFlexible hours$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...- ...for overall project delivery, including clinical trial reports and other regulatory submission... ...that timelines are adhered to and coordinate and lead a statistical programming team... ...other functions (e.g., biostatisticians, data managers, medical writers, etc.) records...Data
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