Clinical Research Project Manager - CRO Trials Lead
Biotrial
Biotrial, a leading provider of high-quality pharmacology services, seeks a Clinical Research Project Manager for Newark, NJ. This role leads clinical trials, ensures regulatory compliance, and coordinates across sponsor, CRO, and Biotrial teams. You will manage timelines, budgets, and study start-up activities, communicating with sponsors and internal teams to drive successful trial execution in a fast-paced environment. #J-18808-Ljbffr Biotrial
- Biotrial, a leading provider of high-quality pharmacology services... ...is currently recruiting a Clinical Research Project Manager for Newark, NJ, US. With... ...and monitoring of clinical trials to ensure that those are conducted... ...Research Organization (CRO) or industry. Experience in...SuggestedContract workWork at office
$115k - $166.5k
...investigating TONMYA® in Phase 2 clinical trials to evaluate its... ...The Senior Clinical Project Manager is responsible for... ...Evaluate and qualify CRO's/vendors/investigator... ...third party vendors Lead regularly scheduled project... ...operations or research with increasing levels...SuggestedTemporary workWork at officeLocal areaFlexible hours$50k - $52k
Clinical Research Coordinator Title: Clinical Research CoordinatorLocation... ..., NJReports to: Manager of Clinical... ...(HKSE), full-service CRO/Contract Research Organization... ...services for clinical trials.Position/Job Summary:... ...and to participate in project team meetings. The...SuggestedContract workTemporary workImmediate start$65k - $78k
...Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional... ...research leadership to support the successful execution, management, and ongoing operations of the vascular medical device observational...SuggestedFull timeTemporary workWork at officeRemote work2 days per week3 days per week$55k - $60k
...Clinical Research Coordinator Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional Service Provider... ...investigator-initiated studies. Manage trials across multiple oncology disease...SuggestedFull timeTemporary workWork at officeRemote workMonday to Friday1 day per week$35 - $38 per hour
...Job Title: Clinical Research Coordinator Job Description We are seeking a dedicated Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves coordinating various aspects of the study process, ensuring...Contract workTemporary work- ...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...Full timeContract work
- Merck & Co. in Rahway, NJ, seeks a Senior Clinical Trial Manager to lead a CRA team of 6-14, ensuring study and site performance with strict ICH... ...is expected; candidates should have 5+ years in clinical research, 3+ years as CRA monitor, and prior line management experience...
- 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
$117k - $184.2k
Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end'... ...across the full our company Research Laboratories portfolio of clinical trials. GCS is accountable for... ...Protocol Clinical Supplies Project Manager (Protocol CSPM)...Full timeFor contractorsLocal areaFlexible hours- 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
$160k - $190k
...CROs, and Sites across the research and clinical trials landscape. By blending deep... ...focus of the role will be leading the operational build-out and... ...growth. Successfully managed cross-functional initiatives... ...relationships with sponsors and CRO partners to enhance site...Full timeTemporary workFlexible hours2 days per week3 days per week- Merck & Co., Inc. in Rahway, NJ is seeking a lead for Clinical Research Associates to manage a team of 6-14 CRAs, ensuring strong trial monitoring, site performance, and adherence to ICH GCP. You will mentor CRAs, coordinate with CRMs, PLMS and HR, and support HQ capacity...
$117k - $184.2k
Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end'... ...across the full our company Research Laboratories portfolio of clinical trials. GCS is accountable for... ...Manager Clinical Supplies Project Manager (IM CSPM) creates...Full timeFor contractorsLocal areaFlexible hours- ...Therapeutic Area (TA) leadership, the CDM (Clinical Data Management) Trial Lead is accountable for end-to-end... ...approaches. •------ Contribute expertise, project management, and/or leadership to... ..., Clinical Data Standards, Clinical Research, Data Analysis, Data Compliance,...Full timeRelocationVisa sponsorshipFlexible hoursShift work
- ...Details Position Information Recruitment/Posting Title Clinical Research Coordinator I Job Category Staff & Executive -... ...Clinical Research Coordinator will support the execution and management of clinical research studies, including coordinating study activities...Full timeSeasonal workWork at officeFlexible hoursShift work
- ...Clinical Research Coordinator III Rutgers, The State University of New Jersey is seeking a Clinical... ...support to the Director, Program Manager and other professional and research staff... ..., and monitoring of departmental projects, ensuring adherence to timelines and attention...Part timeSeasonal workWork at officeShift work
$65k - $80k
...Clinical Research Coordinator Vitalief is a trusted partner to Sponsors, CROs, and Sites across the research and clinical trials landscape. By blending deep subject matter expertise with strong... ...individual who can effectively manage patient-facing responsibilities...Full timeTemporary workWork at officeLocal areaMonday to Friday- ...Merck seeks a Senior Specialist to manage clinical supply chain planning and inventory for global clinical trials. The role involves coordinating end-to-end clinical supply... ...supply experience At least 5 years of project management experience At least 5 years of...Work at office
- Sarepta Therapeutics seeks an Associate Director of Regulatory Labeling and Disclosures to lead global labeling activities and clinical trial disclosures. You will collaborate with cross-functional teams and Health Authorities to ensure compliant labeling and transparency...Remote job
$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... ...role includes coordinating trial activities, managing patient interactions, and ensuring regulatory compliance...$65k - $78k
Vitalief Inc. is looking for a Clinical Research Coordinator (CRC) to support a vascular medical device registry study in Newark, NJ. The... ...$65,000 and $78,000 based on experience. The role includes managing study activities, ensuring compliance, and collaborating with...$282.2k
...DescriptionThe Senior Clinical Director (Senior Principal... ...and directing clinical research activities involving... ...Clinical Director may manage the entire cycle of clinical... ....Planning clinical trials (designing, collaborating... .../external research project teams relevant to the development...Full timeFor contractorsLocal areaVisa sponsorshipFlexible hours$255.8k - $402.7k
...the planning and directing clinical research activities involving new or... ...licensure). The Director will manage the entire cycle of clinical... ...responsible for:Planning clinical trials (design, operational plans,... ...internal/external research project teams relevant to the...Full timeFor contractorsLocal areaFlexible hours$255.8k - $402.7k
Job DescriptionThe Clinical Director (Principal Scientist... ...and directing clinical research activities involving... ...Clinical Director may manage the entire cycle of clinical... ...for:Planning clinical trials (designing,... ...internal/external research project teams relevant to the development...Full timeFor contractorsLocal areaVisa sponsorshipFlexible hours$142.4k - $224.1k
...Description Associate Director, Clinical Supply Project Manager - Program Global Clinical... ...supply chain across our Research & Development Division 's portfolio of clinical trials. GCS is accountable for the... ...to GCS and serves as the lead GCS spokesperson at clinical...Full timeFor contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- Rutgers University seeks a part-time Clinical Research Coordinator III in the Department of Oral... ...support daily operations, coordinate projects, and liaise with multiple departments... ...degree in a relevant field, strong data management skills, and proficiency with Microsoft...Part timeWork at office
- ...The Clinical Operations Program Director is... ...or more clinical research programs .The Clinical... ...complexity of trial designs vs speed)... ...influences all levels of management and cross-... ...the costs resource projections and timelines for... ...million dollars) Leads large scoped cross...Full timeWork experience placementLocal areaRemote work
- ...Transportation Security Officers—or STSOs—manage the people and daily decisions behind airport... ...Transportation Security Officers and Lead Transportation Security Officers, coordinate... ...required to complete a one-year supervisory trial period Must remain available for duty...Permanent employmentFull timeTemporary workTrial periodFlexible hoursShift workNight shiftWeekend workDay shiftAfternoon shiftEarly shift
- ...The Risk Management Lead (RML) serves as the subject matter expert for risk management and central monitoring in AbbVies Risk-Based Quality... ...improvement of risk management practices across global clinical trials partnering closely with study teams and Central Monitoring...Full timeLocal area3 days per week
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