Top 47 Clinical trial manager Jobs in Skillman, Nj

Junior / Lower Mid-Level - Clinical Trial Manager
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- Microsoft Outlook
- English
- Mid-level
Quick Apply
2d
Senior Clinical Trial Manager
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Remote
- Microsoft Outlook
- Computer literacy
- 3 years
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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 Study Associate Manager
Regeneron —Warren, NJ
- $109,900 - $179,300 a year
- Bachelor's degree
- Team management
- Travel
- Health insurance
- Dental insurance
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
Manager, Clinical Pharmacology
EPM Scientific —Princeton, NJ
- $130,000 - $150,000 a year
- Medicine
- 5 years
- Doctor of Philosophy
Quick Apply
2d
Manager, Clinical Study Lead
Regeneron —Warren, NJ
- $128,600 - $210,000 a year
- Microsoft Word
- Microsoft Excel
- 6 years
- Health insurance
- Dental insurance
Sr.Clinical Data Manager
Katalyst Healthcares & Life Sciences —Edison, NJ
- Contract
- Hybrid work
- Nursing
- Bachelor's degree
- Senior level
Quick Apply
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
CLINICAL DATA MANAGER
Zenith LifeScience —South Plainfield, NJ
- $100,000 - $120,000 a year
- Full-time
- Bachelor of Science
- Math
- Bachelor's degree
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
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 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
Manager Study Start Up
Summit Therapeutics —Princeton, NJ
- $139,000 - $163,000 a year
- 5 years
- Administrative experience
- Business Administration
Quick Apply
13d
Manager, Global Scientific Affairs
Abbott Laboratories —Princeton, NJ
- $113,300 - $226,700 a year
- Full-time
- Bachelor's degree
- Continuous improvement
- Doctor of Philosophy
- Health insurance
- Tuition reimbursement
Manager, Clinical Trial Management
Precision for Medicine —Gladstone, NJ
- $133,900 - $200,900 a year
- Online Application
- Remote
- Microsoft Excel
- Microsoft Outlook
- 5 years
Quick Apply
Senior Manager, Clinical Operations
PTC Therapeutics, Inc. —Warren, NJ
- $136,600 - $171,900 a year
- Full-time
- Bachelor's degree
- Children
- Travel
- Dental insurance
- Vision insurance
Quick Apply
9d
Senior Manager, Data Management
Bracco —Princeton, NJ
- Full-time
- 7 years
- English
- Master's degree
Research Program Manager - Oncology
Vitalief —Somerset, NJ
- $115,000 - $145,000 a year
- Full-time
- Nursing
- RN License
- HIPAA
- Paid holidays
- Disability insurance
Quick Apply
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

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clinical trial manager jobs near skillman, nj

Junior / Lower Mid-Level - Clinical Trial Manager

Katalyst Healthcares & Life Sciences -
Edison, NJ

Quick Apply

Job Details

Contract
2 days ago

Qualifications

Customer communication

Full Job Description

Summarized Purpose:

Accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer.
Interprets data on project issues and makes good business decisions with support from experienced team members or line manager.
Works to ensure that all clinical deliverables meet the customer's time/quality/cost expectations.
Maintains profitability by ensuring clinical activity is conducted within contract scope, through efficient management of the clinical team.
Typically works on projects of low to moderate complexity and as part of a team of CTMs.

Essential Functions:

Manages all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
Develops clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan. Contributes to the development of the Master Action Plan (MAP) for providing clinical related documents. Ensures timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central). May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required. Collaborates with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
Collaborates with the clinical team and other departments as needed to meet deliverables of the project. Regularly communicates with the team and leads team meetings to ensure that timelines, resources, interactions, and quality are maintained. Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies. Responsible for the timely archiving of documents and study materials for the department.
Ensures achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution.
Continuously monitors or co-monitors clinical trials to assess performance and ensure contractual obligations are met. In smaller regions, may routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
May communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
May coordinate all start-up activities and ensures that timely ethics committee and regulatory submissions (if appropriate) are addressed. Ensures that essential document quality meets the expectation of Regulatory Compliance Review. Reviews and follows up on all questions raised by the ethics committees.
May provide input into preparation of forecast estimates for clinical activities. Responsible for clinical resource management, assignment, delegation of clinical responsibilities and identification of additional resource requirements.

Knowledge, Skills and Abilities:

Good leadership skills, effective at mentoring and training, and capable of motivating and integrating teams
Good planning and organizational skills to enable effective prioritization of workload
Solid interpersonal and problem-solving skills to enable working in a multicultural matrix organization
Capable of working effectively in a changing environment with complex/ambiguous situations
Familiarity with the practices, processes, and requirements of clinical monitoring
Good judgment and decision-making skills
Effective oral and written communication skills, including English language proficiency
Capable of evaluating workload against project budget and adjusting resources accordingly
Sound financial acumen and knowledge of budgeting, forecasting and fiscal management
Strong attention to detail
Solid understanding of relevant regulations e.g. ICH/GCP, FDA guidelines, etc.
Good computer skills to effectively use automated systems and computerized applications such as Outlook, Excel, Word, etc.

Education and Experience:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years).

Quick Apply

Refine Your Search

clinical trial manager jobs in skillman, nj

Junior / Lower Mid-Level - Clinical Trial Manager

Senior Clinical Trial Manager

Sr. Clinical Trial Manager, Therapeutics and Oncology

Clinical Study Associate Manager

Clinical Data Management Manager

Manager, Clinical Pharmacology

Manager, Clinical Study Lead

Sr.Clinical Data Manager

Clinical Trial Manager/Senior Clinical Trial Manager

CLINICAL DATA MANAGER

Senior Project Manager Clinical Research

Clinical Trial Liaison Manager

Clinical Trial Manager/Senior Clinical Trial Manager

Manager Study Start Up

Manager, Global Scientific Affairs

Manager, Clinical Trial Management

Senior Manager, Clinical Operations

Senior Manager, Data Management

Research Program Manager - Oncology

Contracts Manager, Clinical Supply Services

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