Top 92 Clinical research associate Jobs in Pennington Nj

Clinical Research Associate- West Coast
Zydus Therapeutics Inc. —Pennington, NJ
- $100,000 - $110,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Quick Apply
Temporary Research Assistant
Rutgers University —Piscataway, NJ
- $18 - $25 an hour
- Part-time
- Master's degree
- University
- Bachelor's degree
- Paid holidays
- Dental insurance
DRUG SAFETY ASSOCIATE (multiple openings)
Zenith LifeScience —South Plainfield, NJ
- $98,384 a year
- Full-time
- Mid-level
- Travel
- Scripting
CLINICAL TRIAL ASSOCIATE (multiple openings)
Zenith LifeScience —South Plainfield, NJ
- $98,384 a year
- Full-time
- Mid-level
- Travel
- Experience equivalent to degree accepted
Clinical Research Associate - Part Time
Saint Peter's University Healthcare System —New Brunswick, NJ
- $24.33 - $38.93 an hour
- Part-time
- Hospital
- Mid-level
- Bachelor's degree
- Free parking
- Health insurance
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Clinical Research Coordinator (CRC)
United Theranostics —Princeton, NJ
- $70,000 - $98,000 a year
- Full-time
- 5 years
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
Programming Manager, Clinical Programming
Genmab —Princeton, NJ
- $117,840 - $176,760 a year
- Online Application
- Computer science
- Computer Science
- Writing skills
- Commuter assistance
- Paid parental leave
Associate Director, Clinical Data Management
Genmab —Princeton, NJ
- $157,360 - $236,040 a year
- Online Application
- Analysis skills
- Bachelor's degree
- Mentoring
- Commuter assistance
- Paid parental leave
Senior Manager, Clinical Programming
Genmab —Princeton, NJ
- $131,040 - $196,560 a year
- Online Application
- Computer science
- 6 years
- Computer Science
- Commuter assistance
- Paid parental leave
Director, Data Quality and Process, External Data Clinical Data Management
Genmab —Princeton, NJ
- $189,200 - $283,800 a year
- Online Application
- 5 years
- Bachelor's degree
- Doctor of Philosophy
- Commuter assistance
- Paid parental leave
Clinical Research Nurse Coordinator
Actalent —Somerville, NJ
- $55 - $60 an hour
- Temporary
- Nursing
- RN License
- Bachelor of Science
- Commuter assistance
- Health savings account
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5d
Director, Clinical Data Acquisition Strategy
BMS —Princeton, NJ
- $200,980 - $272,765 a year
- Email
- Hybrid work
- Office
- Analysis skills
- Bachelor's degree
- Paid holidays
- Disability insurance
Director, eCOA Management
BMS —Princeton, NJ
- $200,980 - $243,544 a year
- Email
- Hybrid work
- Office
- Bachelor's degree
- Travel
- Paid holidays
- Disability insurance
Student Assistant (Research), Multiple Vacancies
Rutgers University —New Brunswick, NJ
- $16 an hour
- Part-time
- Microsoft Excel
- Writing skills
- Office
- Paid holidays
- Dental insurance
Clinical Research Specialist - Skin Health/Personal Care (175269)
Colgate-Palmolive —Piscataway, NJ
- $96,800 - $137,000 a year
- Hybrid work
- Mid-level
- Master's degree
- Bachelor's degree
- Profit sharing
- Paid parental leave
7d
Clinical Research Specialist - Skin Health/Personal Care
Colgate-Palmolive —Piscataway, NJ
- $96,800 - $137,000 a year
- Hybrid work
- Mid-level
- Master's degree
- Bachelor's degree
- Profit sharing
- Paid parental leave
7d
Clinical Research Coordinator
Vitalief —New Brunswick, NJ
- $60,000 - $70,000 a year
- Full-time
- Bachelor's degree
- Computer skills
- 1 year
- Paid holidays
- Disability insurance
Quick Apply
Bioinformatics – Assistant to Associate Professor, Non-Tenure Research Track
Rutgers University —New Brunswick, NJ
- From $114,622 a year
- Full-time
- University
- Doctor of Philosophy
- Quality control
- Paid holidays
- Dental insurance
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —Yardley, PA
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Visiting Researcher
Rutgers University —New Brunswick, NJ
- $25,000 - $250,000 a year
- Full-time
- Microsoft Word
- Medicine
- Microsoft Excel
- Paid holidays
- Dental insurance

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Clinical Research Associate- West Coast

Zydus Therapeutics Inc.
Pennington, NJ

Quick Apply

Job Details

$100,000 - $110,000 a year

Qualifications

Computer operation
Microsoft Excel
Microsoft Outlook
Computer literacy
Presentations for conferences or internal meetings
Workplace dispute resolution
Good documentation practices (GDP)
ICH guidelines
Desktop applications
Data interpretation
Clinical quality assurance standards

Full Job Description

Description:

SUMMARY:

Zydus Therapeutics is a clinical stage, specialty-focused bio-pharmaceutical company focused on developing transformative treatments to transform lives, starting with rare and serious liver diseases and anemias.

Our purpose is simple, to empower people with the freedom to live healthier and more fulfilling lives, by unlocking new possibilities in life sciences and providing quality healthcare solutions.

Our lead drug candidate, Saroglitazar, is a liver-selective, dual peroxisome proliferator-activated receptor (PPAR) alpha / gamma agonist. Saroglitazar is an investigational treatment which has received Fast Track designation and orphan drug designation from the US Food and Drug Administration (FDA) for the treatment of patients with primary biliary cholangitis (PBC). Saroglitazar is also an investigational treatment in development for the treatment of non-alcoholic steatohepatitis (NASH). Our second drug candidate is Desidustat, an oral hypoxia-inducible factor prolyl hydroxylase (HIF- PH) inhibitor, an investigational treatment in development for the treatment of chemotherapy-induced anemia (CIA). As a wholly-owned subsidiary of Zydus Lifesciences, our pipeline is fueled by 1,300 researchers who are working with cutting-edge technologies to discover new medicines for tomorrow.

RESPONSIBILITIES:

Responsible for of all aspects of site monitoring activities; Including the conduct of Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), Periodic Monitoring Visits (PMVs) and Close-out Visits (COVs) in accordance with ICH/GCP principles.
Act as the primary contact/ manager for sites to include, but not limited to the following activities:
Provide proper training and guidance to site staff on the protocol and all study related materials
Ensure appropriate safety monitoring, per ICH/GCP principles, are reviewed on an ongoing basis and ensure site has proper oversight of safety reporting requirements
Acts as the primary contact to assigned sites to ensure there is proper compliance to the protocol, adherence to patient safety, proper IP management and study supply management
Review sites recruitment and enrollment activities and assist with recruitment planning and solutions as needed.
Ensure proper review of the sites Investigational Site File Binder and ensure all plans, communications and logs are maintained and updated appropriately as per ICH GCP and GDP requirements
Will provide support to all functional groups (as needed) to ensure proper reporting of safety data and proper site compliance to all protocol and protocol related materials
Will perform site oversight to prevent noncompliance, escalate noncompliance issues and provide guidance/ preventative action plan to prevent future noncompliance as needed

Requirements:

QUALIFICATIONS – SKILLS & REQUIREMENTS:

Must display proper knowledge of ICH GCP principles and GDP knowledge for compliance with document review/ reporting; ALCOA principles
Must be able to demonstrate proper organizational skills and have effective communication skills.
Must be able to work independently managing sites with minimal oversight
Must be able to demonstrate ability to conduct presentations as necessary
Must be able to assist and have experience with oversight of sponsor monitoring activities. This will include: Data interpretation, conflict resolution and demonstration of working with different personnel, & provide guidance and solutions for complex issues
Must have basic knowledge of system tools and web based applications that include, but not limited to:

Microsoft Outlook, Excel, Word and Powerpoint

CTMS, EDC, eTMF and IWRS systems

TRAVEL:

Travel is required for the position; this may be extensive at times (70-80%).

WORK ENVIRONMENT:

This position is remote, but from time to time or when required, the employee will be required to report to our office, located in our office in Pennington, NJ. The physical demands described here are representative of those that must be met by an individual to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the individual is:

Frequently required to sit and/or stand, walk, talk, and hear.
Ability to sit at a computer for an extended period of time.
Vision ability requirements include clarity of visions at 20 inches or less due to computer work.
Moderate noise (i.e., background noise due to computers, phone, printers, and light hallway traffic).
Constantly required to use hands and fingers to operate office machines and equipment.
Frequently required to reach with hands and arms. Occasionally required to stoop, kneel, and crouch.

The work environment characteristics described here are representative of those that an individual encounters while performing the essential functions of this job.

Zydus Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Zydus is committed to providing reasonable accommodation to, among others, individuals with disabilities and disabled veterans. If you need an accommodation because of a disability to search and apply for a career opportunity with Zydus, please contact us and let us know the nature of your request.

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Refine Your Search

clinical research associate jobs in pennington nj

Clinical Research Associate- West Coast

Temporary Research Assistant

DRUG SAFETY ASSOCIATE (multiple openings)

CLINICAL TRIAL ASSOCIATE (multiple openings)

Clinical Research Associate - Part Time

Clinical Research Coordinator (CRC)

Programming Manager, Clinical Programming

Associate Director, Clinical Data Management

Senior Manager, Clinical Programming

Director, Data Quality and Process, External Data Clinical Data Management

Clinical Research Nurse Coordinator

Director, Clinical Data Acquisition Strategy

Director, eCOA Management

Student Assistant (Research), Multiple Vacancies

Clinical Research Specialist - Skin Health/Personal Care (175269)

Clinical Research Specialist - Skin Health/Personal Care

Clinical Research Coordinator

Bioinformatics – Assistant to Associate Professor, Non-Tenure Research Track

Senior Clinical Research Associate (level dependent on experience)

Visiting Researcher

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