280 Results for

Clinical Trial Manager Jobs in New Jersey

Jobs

Basking Ridge, NJ8 days ago

$136,080–$204,120 Per Year
Full-time

CRO Oversight: Responsible for the oversight, performance, and management of CRO(s) and 3rd party vendors (sub-contracted by CRO) to ensure compliance with Daiichi Sankyo’s quality measures and adherence to scope of work within timelines and budget at a task level. Clinical Operations Study Management(Global) has primary accountability for operational execution and delivery of assigned clinical trials, including study level time, cost and quality deliverables.

Basking Ridge, NJ15 days ago

$133,600–$200,400 Per Year
Full-time

Basking Ridge, NJ15 days ago

$133,600–$200,400 Per Year
Full-time

Basking Ridge, NJ15 days ago

The Associate Director, Clinical Database Applications and Reporting is a member of the Biostatistics and Data Management team and serves as a subject matter expert responsible for setting the overall programming strategy including the oversight, guidance, implementation, and management of clinical database applications and reporting. Work Experience: Minimum of 7 years of global clinical trial experience in the device/pharmaceutical/CRO industry with expertise in clinical database programming, methods, and techniques supporting Clinical Data Management systems and services required.

New!

Parsippany, NJ3 days ago

$100,000–$130,000 Per Year
Full-time
Employee

Directly and effectively partner and collaborate with DSA and DSI Supply Chain, Field Support, Training, Marketing, Quality and Legal to strengthen relationships and mutual trust. Develop, with Director of Market Access, key metrics for staff to ensure project timeliness and manage staff adherence to timelines.

New!

Hoboken, NJ1 day ago

$350,000–$400,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. 4. Collaborate with cross-functional teams including regulatory affairs, pharmacovigilance, and medical affairs to ensure a holistic approach to product development.

Basking Ridge, NJ15 days ago

$100,960–$151,440 Per Year
Full-time

Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor performance against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Job Description. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders.

Basking Ridge, NJ15 days ago

Develop and validate datasets and Tables, Listings, and Figures (TLFs) to ensure high-quality deliverables for pivotal studies, as well as Integrated Summary of Efficacy (ISE) and Integrated Summary of Safety (ISS) for oncology regulatory submissions. This role ensures the quality, consistency, and timeliness of deliverables supporting oncology regulatory submissions by guiding programming strategies, reviewing key outputs, and driving issue resolution.

New!

Jersey City, NJ2 days ago

The Clinical Development Executive Medical Director is the clinical leader of the specific clinical programs assigned with responsibility for outlining the overall clinical development strategy in line with regulatory requirements and sound scientific rationale, designing the clinical protocols, guiding the Clinical Operations team towards the adequate implementation of such protocols, ensuring adequate medical monitoring activities are implemented for the conduction of clinical studies and analyzing the data from the clinical program. The individual will also be responsible for ensuring adequate implementation of the global safety surveillance and pharmacovigilance for the investigational products, including review and analysis of safety data from clinical trials and other permitted sources (e.g., early access/expanded access programs, if applicable), identification and investigation of safety signals, and management of the benefit-risk profile for assigned compounds.

New!

Basking Ridge, NJ1 day ago

$127,280–$190,920 Per Year
Full-time

Become a Subject Matter Expert (SME) with the process currently in use; be able to describe to study teams and other key departments how their study will interact with the adjudication vendor; Describe the expectation and importance of adjudication between the vendor to the CRO; Become an active “extended team member” to multiple studies at the same time; Being extremely organized to discuss with studies at different timepoints. Support analysis of study site ILD adjudication metrics reports to identify potential areas of concern, trends, missing eDC pages, issues with image uploading; bring to the attention of the Study Team / CRO; offer solutions.

Basking Ridge, NJ15 days ago

$201,840–$302,760 Per Year
Full-time

They are accountable to ensure their direct reports are delivering to agreed upon study plans, properly identifying risks/mitigations, escalating as appropriate and utilizing data and metrics to put appropriate strategies and plans in place as well as measuring the status/variance of a study and putting appropriate measures in place to course correct where needed. They will ensure their direct reports are meeting required study deliverables including but not limited to oversight of CROs and Vendors and (as applicable) properly leading and ensuring delivery of milestones for the studies within assigned program(s).

Basking Ridge, NJ15 days ago

$242,700–$404,500 Per Year
Full-time

Lead scientist team to collaborate with safety physicians, regulatory affairs, clinical development, other functions and external partners to deliver high-quality safety assessments, regulatory submissions, aggregate reports, and responses to health authority queries. In addition to operational oversight, this role contributes to the development of global safety processes, talent capability building, and strategic alignment across the broader Clinical Safety and Pharmacovigilance (CSPV) function and the enterprise.

Basking Ridge, NJ14 days ago

$150,800–$226,200 Per Year
Full-time

Provide operational QA leadership for the respective CSPV teams, including Quality Oversight for the Quality Plan execution, review of key CSPV regulatory documents, Health Authority Commitments, Critical Incidents including, respective escalation process and the CAPA Management Process for the respective CSPV functional areas. Interact with senior CSPV leadership teams to ensure Quality is consistently and proactively represented at program level and along the clinical trial process in support of a proactive quality risk management process.

Basking Ridge, NJ13 days ago

$271,500–$452,500 Per Year
Full-time

Provides regular status updates on projects, metrics and KPIs to Head of BDM and BDM LT External Vendor Oversight: Provides oversight of and is accountable for the quality/performance and budget, resources and timelines across the department and ensures timely delivery of high-quality deliverables at reasonable cost. This role also serves as a key member of the BDM leadership team, contributing to BDM broader organizational strategy, cross-functional decision-making, and the advancement of BDM objectives beyond the Biostatistics function.

New!

New Brunswick, NJ1 day ago

RWJBarnabas Health, the largest and most comprehensive integrated healthcare system in New Jersey, and a proud partner of Rutgers Cancer Institute of New Jersey—New Jersey’s only NCI-designated Comprehensive Cancer Center—is actively recruiting a full-time Attending Medical Oncologist specializing in Genitourinary (GU) Malignancies to join our dynamic oncology team. Our partnership with Rutgers University creates the state’s largest academic healthcare system dedicated to providing high-quality patient care, leading-edge research, and world-class health and medical education, further advancing our mission of providing high-quality healthcare in New Jersey.

New!

Warren, NJ2 days ago

This individual serves as the regulatory affairs main contact to project teams, providing leadership across functions for regulatory strategic planning and execution related to achieving program milestones. Oversees the day-to-day operations within the regulatory affairs function including oversight of submission coordination, submission publishing, advertising/promotional review, and process development/improvement initiatives.

New!

New Brunswick, NJ1 day ago

Our partnership with Rutgers University creates the state’s largest academic healthcare system dedicated to providing high-quality patient care, leading-edge research, and world-class health and medical education, further advancing our mission of providing high-quality healthcare in New Jersey . With 12 acute care hospitals, 3 children's hospitals, a growing number of our outpatient facilities and physician practices, our healthcare system is committed to providing the highest quality of patient care and health education to the community and region.

New!

Jersey City, NJ3 days ago

Collaboration: Develop and nurture professional relationships with physicians and staff at JSUMC and other Hackensack Meridian Health (HMH) campuses, including Ocean University Medical Center (OUMC), to promote practice growth to Bayshore Medical Center (BMC). ? The posted rate of pay in this job posting is a reasonable good-faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.

East Windsor, New Jersey26 days ago

Physical Requirements: OFFICE POSITION - While performing the duties of this job the employee is required to: •Stand, sit; talk, hear, and use hands and fingers to operate a computer and telephone keyboard reach, stoop kneel to install computer equipment •Specific vision abilities required by this job include close vision requirements due to computer work •Light to moderate lifting is required •Moderate noise (i.e. business office with computers, phone, and printers, light traffic). Job Overview: The Clinical Trial Manager will lead key aspects of assigned clinical trial(s) and demonstrates a good level of knowledge of clinical methodologies, organizational, project management and leadership capabilities.

Princeton, NJ30+ days ago

Full-time

For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.

Princeton, NJ30+ days ago

Full-time

New Brunswick, NJ30+ days ago

Remote

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNP. KEY RESPONSIBILITIESIndependently review, interpret, negotiate, and process clinical trial agreements, nondisclosure agreements, and related contracts from legal, business, and technical perspectives, ensuring alignment with institutional policies and sponsor requirements.

New Brunswick, NJ28 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. Vitalief partners with Sponsors, CROs, and research sites across the clinical trials ecosystem, delivering consulting and workforce solutions that improve efficiency, reduce costs, and accelerate patient-impacting innovation.

Princeton, NJ30+ days ago

$308,700–$374,075 Per Year

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. • In collaboration with the Clinical Development Lead, designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets.

Princeton, NJ30+ days ago

$350,780–$425,060 Per Year

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. • A Senior Clinical Trial Physician II is a tenured drug developer who can independently design and construct clinical development plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets.

Princeton, NJ30+ days ago

$96,940–$117,472 Per Year

Issues Manufacturing and Packaging/Labeling requests to Clinical Supply Operations (CSO) in alignment with RDSC Master Planning timelines and based on collaboration with Clinical Development team, Chemistry, Manufacturing & Controls (CMC) team and CSO Packaging and Labeling to ensure package design and clinical label for investigational product meet protocol and regulatory requirements. Actively participates in internal Trial Supply Management and Clinical Supply Chain meetings, Study Team meetings, Clinical Supply Matrix Team meetings and any other relevant meetings providing all relevant data and documentation prior to each meeting, highlighting any risks and mitigation strategies.

Florham Park, New Jersey13 days ago

$135,000–$165,000 Per Year

The role encompasses supporting study risk assessments and defining RBQM study needs and strategies, which include determining the frequency and requirements for onsite versus remote monitoring activities, targeted SDV and SDR, and fostering constructive collaboration with cross-functional teams such as biometrics/data management, eTMF, and medical/safety monitoring. Review and collaborate to develop fit-for-purpose study plans that define risk-based monitoring strategies and the related tasks necessary to oversee critical study data and process (e.g., clinical monitoring plan, centralized monitoring plan, protocol deviation management plan, and integrated quality risk management plan).

New!

Mahwah, NJToday

Leading people who perform project management duties involving cross-functional teams focused on delivering internal products or administrative systems. Organizing project activities and interdepartmental meetings, ensuring communication facilitates the completion of the program or project on schedule and within budget constraints.

Trenton, NJ30+ days ago

Remote

The Project Manager drives the planning, execution, and delivery of internal initiatives across Study Management functions and reports directly to the Director, Clinical Operations. + Demonstrated end‑to‑end clinical trial management experience across Phase II and Phase III studies, with strong understanding of operational requirements from study start‑up through close‑out.

Parsippany-Troy Hills, NJ30+ days ago

Contractor

Job Title - Manager, Vendor Outsourcing Location: Parsippany, NJ (HM Site); Foster City, CA; Santa Monica, CA HYBRID - Onsite 3 days a week - T/W/Th Functional Area: Development Operations, Vendor Outsourcing Position Type: Full Time Equivalent Department: Vendor Outsourcing ***, Inc. is a research-based biopharmaceutical company founded in 1987. As part of our rapidly growing science-driven organization, colleagues at Client are revolutionizing healthcare by bringing urgently needed medicines to patients in the areas of Virology, Inflammation and Oncology conditions.

Parsippany, NJ11 days ago

$85,000–$100,000 Per Year

The ideal candidate for our Clinical Outcome Technology Project Manager position has great communication skills, is self-motivated and passionate about their work, has a strong desire to grow professionally, possesses an eagerness to be part of a dynamic group of focused and creative individuals and has excellent time management skills. Canfield Scientific, Inc. is a core imaging lab providing custom photographic systems, image monitoring, and centralized analysis services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting documentation.

Princeton, NJ30+ days ago

$139,570–$169,126 Per Year

The role combines strong full‑stack engineering capabilities with AI product thinking, technical roadmap ownership, and close partnership with product managers and business stakeholders to deliver measurable outcomes for patients and teams. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

Princeton, NJ30+ days ago

$257,180–$311,647 Per Year

In this steady-state model, the Executive Director ensures that the Trial Analytics function delivers actionable insights, innovative analytic solutions, and continuous performance improvements that accelerate clinical trials across the full development lifecycle, forecast timeline expectations, manage changing landscapes to optimize resource use, and ultimately bring life-changing therapies to patients faster. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

Hackensack, New Jersey30+ days ago

Responsibilities: A day in the life of a Senior Trauma Clinical Data Coordinator at Hackensack Meridian Health includes: Works in collaboration with Trauma principal investigators, sub-investigators, Trauma Research RN, and regulatory specialists on all research issues ensuring adherence to trauma research protocols. Qualifications: Education, Knowledge, Skills and Abilities Required: Bachelor of Arts/Bachelor of Science diploma/degree in science or healthcare field OR minimum of 4+ years of experience in a related area with High School diploma, general equivalency diploma (GED), and/or GED equivalent programs.

Princeton, NJ30+ days ago

Full-time

It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.

Princeton, NJ30+ days ago

Full-time

For 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. In close partnership with the Head of Function, this roledrives portfolio levelCRO/clinicalvendorperformance management acrossall ClinicalTrialDelivery,operating model refinement, and process innovation initiatives that enhance scalability, predictability, and quality of trial delivery.

Plainsboro Township, New Jersey30+ days ago

$115,000–$130,000 Per Year

Train and support external trial staff regarding CRF and IVRS data entry, AE/SAE/MESI reporting, ethics reporting, protocol deviation identification, drug accountability, temperature monitoring, query resolution, essential document collection, and ITF filing. Collaborate with Local Trial Manager (LTM) and Line of Business Manager, communicating site progress and escalating critical issues impacting trial milestones.

New Brunswick, NJ30+ days ago

Remote

Full-time

Proven success in building strong executive-level and C-suite relationships while leading a multi-faceted change process; demonstrated broad-based change management expertise and extensive experience positively influencing change in a variety of complex environments with multiple stakeholders and competing priorities. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

New Brunswick, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNP. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

Princeton, NJ30+ days ago

$133,710–$162,019 Per Year

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Technical Proficiency: Proficiency in Python (R or Julia), with hands-on experience with ML frameworks (Scikit-Learn, TensorFlow, PyTorch, etc.) Experience with agentic AI frameworks (Strands, LangGraph, AutoGen, DSPy, CrewAI, or similar).

Princeton, NJ30+ days ago

$214,020–$259,344 Per Year

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Key responsibilities of this role are to act as a lead scientist to implement and deliver on biomarker strategies for clinical programs, develop reports and publications on translational data generated to support asset development and contribute to regulatory submissions.

New Brunswick, NJ24 days ago

Remote

Part-time

The ideal candidate brings deep expertise in organizational transformation and change management within complex healthcare and research environments, with a proven ability to drive stakeholder alignment, operational adoption, and sustainable process improvement across multi-site systems. Conduct in-depth interviews with clinical research staff and stakeholders across the clinical trial lifecycle to identify operational gaps, bottlenecks, communication challenges, and improvement opportunities across Oncology and Non-Oncology programs.

Princeton, NJ30+ days ago

$166,600–$201,880 Per Year

The individual will drive the strategic partnership with the teams within the Global MAx and GTN Finance organizations, to identify digital capabilities, build comprehensive business cases that have the greatest impact on the enterprise, set the right expectations, and ensure that IT resources are appropriately engaged to fulfill the intended business outcomes. This position is the BI&T, Commercialization Gross-to-Net Product Manager partnering with the Global MAx Pricing teams (for Oncology, CV, Immunology & Fibrosis, Hematology and Cell Therapy), accountable for supporting the strategic planning, design, integration and delivery of digital capabilities to enable gross-to-net solutions in the US.

Princeton, NJ30+ days ago

$119,600–$144,921 Per Year

This individual will work with the Commercial Distribution Category Leads and Partners to develop a Wholesaler strategy that aligns to the strategic priorities of BMS and ensure that the strategy can meet business needs across the product lifecycle and across markets. Collaborate with Category Leads and Partners to ensure category strategies are effectively supporting business outcomes such as product launch, in-line product growth, upcoming LOEs, and data and insights.

New Brunswick, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. Vitalief partners with Sponsors, CROs, and research sites across the clinical trials ecosystem, delivering consulting and workforce solutions that improve efficiency, reduce costs, and accelerate patient-impacting innovation.

Princeton, NJ30+ days ago

$147,900–$184,900 Per Year

Prepares/oversees the preparation of all applicable documents required for the conduct of the study (Project Plan, Risk Management Plan, Monitoring Plan, Trial Master File (TMF)) etc.* Manages and reviews the work of Contract Research Organization (CRO) to ensure that tasks are performed to scope and budget.* We are developing the next wave of therapeutic advancements with a robust and diverse pipeline that includes mid- to late-stage programs in Alzheimer's disease psychosis and Lewy body dementia psychosis, along with earlier-stage programs that address other underserved patient needs.

Teaneck, NJ30+ days ago

$83,990.40–$104,998.40 Per Year
Full-time

In this role, the QA/QI Manager is expected to deliver a structured and sustainable quality framework that includes routine risk-based internal audits, timely identification and remediation of compliance gaps, development and tracking of CAPAs, maintenance of training documentation, and preparation for sponsor, FDA, or external inspections. A key deliverable of this role is an annual QA/QI Workplan that outlines prioritized quality initiatives, defines measurable objectives and audit schedules, assigns clear ownership, and establishes timelines and reporting mechanisms to ensure ongoing regulatory compliance, operational integrity, and continuous process improvement across the clinical research portfolio.

Parsippany, New Jersey30+ days ago

$103,000–$140,000 Per Year

Write, test, and validate SAS programs to produce analysis datasets, TLGs and presentation output, to be included in reports for submission to regulatory agencies, publications and other communications as needed. The range considers a wide range of factors that are considered in making compensation decisions, including but not limited to: geographic markets, business or organizational needs, skill sets, experience, training, licensure, and certifications.

New Brunswick, NJ30+ days ago

Remote

Part-time

This role will serve as the primary subject matter expert (SME) for a comprehensive current-state operational assessment across Technology, Organization, Process, People, and Finances, with a strong focus on Non-Oncology programs and cross-system communication effectiveness. Conduct in-depth interviews with clinical research staff and stakeholders across the trial lifecycle to identify gaps, bottlenecks, and improvement opportunities for Non-Oncology operations.

New!

Piscataway, NJ2 days ago

$250,000–$275,000 Per Year

Develop new clinical indices and biochemical assessments and apply a broad range of established dental assessment indices (e.g., caries, plaque, gingivitis, periodontology, sensitivity, whitening, calculus, oral malodor, anti-bacterial or others) to design, evaluate, and differentiate clinical programs and product performance that are superior to, existing products. The ideal candidate is an internationally renowned expert in oral health and dental clinical research, with substantial industry and/or academic experience, a proven track record of leading clinical programs, and demonstrated strength in people leadership and collaborative partnerships.

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Clinical Trial Manager Jobs in New Jersey

Clinical Study Manager, Clinical Operations Daiichi Sankyo, Inc.

Clinical Study Manager, Global Clinical Operations Daiichi Sankyo, Inc.

Clinical Study Manager, Global Clinical Operations - 30014765 Daiichi Sankyo, Inc.

Senior Manager, Clinical Database Applications and Reporting (m/f/d) Daiichi Sankyo, Inc.

Manager, Scientific Affairs Company Confidential

Vice President Clinical Development Ophthalmology Jobot

Sr Clinical Study Assoc CO Daiichi Sankyo, Inc.

Manager, Statistical Programming (m/f)d) Daiichi Sankyo, Inc.

Executive Medical Director, Clinical Development - M.D. (Nephrology) Clinical Dynamix, Inc.

Manager, Clinical Adjudication Operations Daiichi Sankyo, Inc.

Dir Clinical Operations Non-MD Daiichi Sankyo, Inc.

Senior Director, Clinical Safety Scientist Daiichi Sankyo, Inc.

Associate Director PV Quality, Americas Daiichi Sankyo, Inc.

Head of Global Biostatistics Daiichi Sankyo, Inc.

RWJBarnabas Health is Seeking a Medical Oncologist in Central and Northern New Jersey RWJBarnabas Health

Director, Regulatory Affairs Strategy Aquestive Therapeutics

RWJBarnabas Health is Hiring Hematologists/Oncologists Across New Jersey! RWJBarnabas Health

Urogynecologist Hackensack Meridian Health

Clinical Trial Manager Acrotech Biopharma Inc

Senior Clinical Trial Manager Genmab

Clinical Trial Manager Genmab

Clinical Trials Contracts Manager Vitalief

Associate Director of Oncology Clinical Trials Nursing Vitalief

Senior Clinical Trial Physician/Clinical Trial Physician (Pulmonology) Bristol Myers Squibb

Senior Clinical Trial Physician II, Cardiovascular Bristol Myers Squibb

Manager, Trial Supplies Management Bristol Myers Squibb

Senior Manager, Clinical Monitoring Oversight Shionogi Inc.

Clinical Research Project Manager iMPact Business Group, Inc.

Clinical Project Manager - East Coast US - FSP Parexel

Manager, Clinical Contracts & Finance - II* Integrated Resources, Inc

Clinical Outcome Technical Project Manager (ONSITE) Canfield Scientific, Inc

Senior Manager, Full Stack Engineer, Clinical Engineering & Operations Bristol Myers Squibb

Executive Director, Head Trial Analytics, Insights and Planning Bristol Myers Squibb

Senior Trauma Clinical Data Coordinator - Full Time - Day Hackensack Meridian Health

Global Director, Clinical Project Management Systimmune

Director, Strategic Clinical Vendor Oversight and Relationship Lead (CRO) Genmab

Senior Clinical Research Associate System One

Vice President, Clinical Research FSP Consulting Vitalief

Clinical Research Coordinator Vitalief

Senior Manager, Intelligence Systems Lab Bristol Myers Squibb

Associate Director, Oncology Clinical Biomarker Asset Lead, Translational Development Bristol Myers Squibb

Clinical Research Change Management Consultant Vitalief

Associate Director – BI&T, Commercialization Gross-to-Net Product Manager Bristol Myers Squibb

Senior Manager, Procurement, Wholesalers Bristol Myers Squibb

Oncology Clinical Research Nurse Director Vitalief

Associate Director Clinical Operations ACADIA PHARMACEUTICALS INC

Quality Assurance/Quality Improvement Manager - Full Time Holy Name Medical Center

Manager, Statistical Programming Pacira Pharmaceuticals, Inc.

Clinical Research Strategic Management Consultant Vitalief

Sr. Director, Clinical Research (Piscataway, NJ, US) Colgate-Palmolive Company

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