Top 123 Clinical trial manager Jobs in South Plainfield Nj

Senior Clinical Trial Manager
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Remote
- Microsoft Outlook
- Computer literacy
- 3 years
Quick Apply
Junior / Lower Mid-Level - Clinical Trial Manager
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- Microsoft Outlook
- English
- Mid-level
Quick Apply
3d
Clinical Trial Liaison Manager
Recordati —Bridgewater, NJ
- $109,800 - $164,700 a year
- Weekends as needed
- Hybrid work
- 5 years
- English
- Mid-level
- AD&D insurance
- Paid holidays
CLINICAL DATA MANAGER
Zenith LifeScience —South Plainfield, NJ
- $100,000 - $120,000 a year
- Full-time
- Bachelor of Science
- Math
- Bachelor's degree
Sr. Clinical Trial Manager, Therapeutics and Oncology
Moderna, Inc. —Princeton, NJ
- $130,800 - $209,400 a year
- Full-time
- 5 years
- Office
- Bachelor's degree
- Paid time off
- Adoption assistance
Clinical Trial Manager/Senior Clinical Trial Manager
Precision Medicine Group —Gladstone, NJ
- $110,700 - $200,900 a year
- Online Application
- Remote
- 7 years
- Microsoft Excel
- Microsoft Outlook
9d
Clinical Trial Manager/Senior Clinical Trial Manager
Precision for Medicine —Gladstone, NJ
- $110,700 - $200,900 a year
- Online Application
- Remote
- 7 years
- Microsoft Excel
- Microsoft Outlook
Quick Apply
9d
Title Clinical Trial Liaison Manager
Recordati —Bridgewater, NJ
- $109,800 - $164,700 a year
- Weekends as needed
- Hybrid work
- 5 years
- English
- Mid-level
- AD&D insurance
- Paid holidays
Clinical Program Manager
IQVIA —Parsippany-Troy Hills, NJ
- $93,100 - $285,500 a year
- Full-time
- Remote
- Bachelor's degree
- Conflict management
- Senior level
- Work from home
Clinical Trial Manager
Genmab —Princeton, NJ
- $119,120 - $178,680 a year
- Online Application
- 5 years
- Master's degree
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Senior Clinical Trial Manager
Genmab —Princeton, NJ
- $130,720 - $196,080 a year
- Online Application
- Master's degree
- 8 years
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Contracts Manager, Clinical Supply Services
Catalent —Bridgewater, NJ
- $122,000 - $160,000 a year
- Email
- Writing skills
- Mid-level
- Office
- Paid holidays
- Health insurance
5d
Clinical Data Management Manager
Integra LifeSciences —Princeton, NJ
- $109,250 - $149,500 a year
- Email
- Hybrid work
- Data analysis skills
- Office
- Analysis skills
- Disability insurance
- Health insurance
Senior Clinical Drug Supply Manager
Amneal Pharmaceuticals —Bridgewater, NJ
- $170,000 - $190,000 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
- Health insurance
- 401(k) matching
3d
Clinical Program Manager
Kite Pharma —Parsippany-Troy Hills, NJ
- $165,495 - $235,620 a year
- Full-time
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Dental insurance
Clinical Study Associate Manager
Regeneron —Warren, NJ
- $109,900 - $179,300 a year
- Bachelor's degree
- Team management
- Travel
- Health insurance
- Dental insurance
Senior Clinical Trial Manager, Oncology
Eikon Therapeutics —Jersey City, NJ
- $143,000 - $173,250 a year
- 6 years
- Office
- Master's degree
- AD&D insurance
- Paid holidays
Quick Apply
11d
Senior Manager, Clinical Data Systems
AbbVie —Florham Park, NJ
- $124,500 - $236,500 a year
- Full-time
- Hybrid work
- Computer Science
- Master's degree
- SQL
- Paid holidays
- Health insurance
Sr.Clinical Data Manager
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- Hybrid work
- Nursing
- Bachelor's degree
- Senior level
Quick Apply
Senior Project Manager Clinical Research
Abbott Laboratories —Princeton, NJ
- $86,700 - $173,300 a year
- Full-time
- Office
- Bachelor's degree
- Doctor of Philosophy
- Health insurance
- Tuition reimbursement

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Senior Clinical Trial Manager

Katalyst Healthcares & Life Sciences -
South Plainfield, NJ

Quick Apply

Job Details

Contract

Qualifications

Microsoft Outlook
Drug regulation
ICH guidelines
Project management experience in healthcare
Managing clinical research teams
Clinical trial standard operating procedures
Managing projects
Clinical quality assurance standards
Pharmaceutical research experience
Standard operating procedures (SOPs)
FDA regulations
Standard operating procedures drafting

Full Job Description

Position Summary:

seeking a highly motivated Sr. Clinical Trial Manager (SCTM) to be part of our Clinical Operations team. This is a unique opportunity to join a growing company committed to converting biologics and peptides into life-changing small molecule medicines for everyone. Needs to be able to work PST Hours.
The SCTM will be responsible for the day-to-day oversight of global clinical trials and will manage internal stakeholders, CROs, multiple service providers, clinical monitors, and clinical trial sites. The SCTM will focus on the management and support of multinational, multicenter, late stage studies and may assume responsibility for additional studies/indications as applicable.
The SCTM works closely with and supports the Clinical Development Operations team, receives assignments in the form of objectives, and will ensure deliverables are completed on time and within budget.
This position will also work closely with a cross-functional team based in the US and Shanghai to ensure that clinical trials are conducted in a timely fashion and compliant with SOPs, ICH/GCP, Country specific regulatory guidelines, company goals, and budgets.
The SCTM will be responsible for managing various project goals and supporting delivery of a quality clinical trial to meet current business needs and trends.

Job Responsibilities:

Leads and coordinates global cross-functional study teams through all study stages (start-up, conduct, close-out).
In collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers, budgets and proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements).
Provides oversight and direction to the CRO and service providers to accurately coordinate clinical study activities.
Assists with Inspection Readiness activities which may require the development, modification and/or implementation of policies as needed to ensure high quality and integrity in all study activities.
Coordinate clinical study timelines with Project management and escalate issues that may impact timelines/ deliverables.
Leads and/or participates in the development and review of study documents including, but not limited to, CRF design, project plans, Service Provider Oversight plans, TMF plan.
Follows processes and procedures and recommend changes to SOP's and policies to ensure comprehensive and compliant processes in the clinical operations organization.
Identifies potential study issues/risks, escalates as needed and recommends/implements
Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review/clean up.
Coordinate with Lead and Finance to track the financial status against budget.
Provide regular updates to Study Lead and other stakeholders; Proactively identify, manage, or escalate issues appropriately.
Prepares or reviews clinical sections of regulatory submission documents, responses to EC and/or Health Authority questions.
Monitors study progress for possible changes in study scope to ensure timely change order implementation and finalization; implementation of PI Training, site monitor training, etc.
May have some responsibility for the oversight and management of the study budget including site and service provider budgets.
Supervises ongoing communication of operational issues and provides accurate progress reports on assigned activities to Study Management Team and Clinical Development Team.
Ensures oversight of data and information in study specific systems EDC, CTMS, eTMF is current and accurate.
May lead a cooperative effort on a project team or contribute as a subject matter expert on key projects and initiatives to identify and implement process improvements and standards.
Other supportive duties as assigned to achieve operational

Experience:

Minimum of 7+ years of related industry experience as a Clinical Research Associate or related function with increasing responsibility and scope
Minimum of 3+ years study management experience in clinical and drug development
Experience in selecting, managing, and overseeing sites, CROs, specialty labs and other service providers in global, multinational studies or programs.
Experience in supporting SOP development and implementation is
Experience working on global teams is desired, Asia-Pacific and EU highly

Core Competencies, Knowledge, Skill Requirements and Education:

PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)
In-depth understanding of FDA and EU regulations, ICH Guidelines and GCP requirements governing the conduct of clinical trials.
Bachelor's degree or equivalent (scientific or healthcare discipline preferred)

Quick Apply

Refine Your Search

clinical trial manager jobs in south plainfield nj

Senior Clinical Trial Manager

Junior / Lower Mid-Level - Clinical Trial Manager

Clinical Trial Liaison Manager

CLINICAL DATA MANAGER

Sr. Clinical Trial Manager, Therapeutics and Oncology

Clinical Trial Manager/Senior Clinical Trial Manager

Clinical Trial Manager/Senior Clinical Trial Manager

Title Clinical Trial Liaison Manager

Clinical Program Manager

Clinical Trial Manager

Senior Clinical Trial Manager

Contracts Manager, Clinical Supply Services

Clinical Data Management Manager

Senior Clinical Drug Supply Manager

Clinical Program Manager

Clinical Study Associate Manager

Senior Clinical Trial Manager, Oncology

Senior Manager, Clinical Data Systems

Sr.Clinical Data Manager

Senior Project Manager Clinical Research

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