Top 26 Clinical research associate remote Jobs in New Jersey

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
Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)
IQVIA —Parsippany-Troy Hills, NJ
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
Coordinator / Senior Coordinator, Project Services - Laboratories (Remote - East Coast)
IQVIA —Parsippany-Troy Hills, NJ
- $44,500 - $111,800 a year
- Full-time
- Remote
- English
- Mid-level
- Microsoft Office
- Work from home
Job Posting Title Clinical Trial Psych Rater - Italian Speaking
IQVIA —New Providence, NJ
- $41,000 - $61,400 a year
- Part-time
- Remote
- Nursing
- Medicine
- Psychiatry
- Work from home
3d
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
14d
Associate Director, Clinical Data Management
Insmed Incorporated —Bridgewater, NJ
- $164,000 - $213,000 a year
- Full-time
- Remote
- 3 years
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Disability insurance
14d
Sr Project Specialist (Sponsor Dedicated/Remote)
サイネオス・ヘルス —New Jersey
- $47,000 - $79,900 a year
- Remote
- English
- Senior level
- Employee stock purchase plan
- Health insurance
11h
Clinical Project Manager - Oncology (Client Dedicated/Remote)
サイネオス・ヘルス —New Jersey
- $120,000 - $135,000 a year
- Remote
- Mid-level
- 3 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Head of Clinical Data Management
Insmed Incorporated —Bridgewater, NJ
- $255,000 - $347,500 a year
- Full-time
- Remote
- Computer Science
- Master's degree
- 8 years
- Employee stock purchase plan
- Disability insurance
Sr. Clinical Project Manager, IQVIA Biotech
IQVIA —Parsippany-Troy Hills, NJ
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Clinical Scientist - Ophthalmology
サイネオス・ヘルス —New Jersey
- Remote
- Mid-level
- Employee stock purchase plan
- Health insurance
Clinical Scientist - Cardiovascular
サイネオス・ヘルス —New Jersey
- Remote
- Mid-level
- Cardiology
- Employee stock purchase plan
- Health insurance
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 Clinical Trial Manager
Katalyst Healthcares & Life Sciences —South Plainfield, NJ
- Contract
- Remote
- Microsoft Outlook
- Computer literacy
- 3 years
Quick Apply
Clinical Scientist - Immunology (Expertise in Ulcerative Colitis, Crohn’s disease and Rheumatology + Excel) - Clinical Drug Trial Exp - Must Have
サイネオス・ヘルス —New Jersey
- Remote
- Senior level
- Employee stock purchase plan
- Health insurance
Clinical Trial Manager - Full Service
サイネオス・ヘルス —New Jersey
- Remote
- Computer literacy
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Health insurance
4d
Associate Director Radiopharmaceutical Clinical Applications – Mid-Atlantic (NJ, PA, Washington DC, MD, DE)
Lantheus Medical Imaging Inc —Somerset, NJ
- $163,000 - $245,000 a year
- Remote
- Microsoft Word
- Hospital
- Bachelor's degree
- Paid parental leave
- Paid holidays
Quick Apply
Clinical Database Designer I
Everest Clinical Research —Bridgewater, NJ
- $50,000 - $90,000 a year
- Remote
- Computer science
- Computer Science
- Bachelor of Science
- AD&D insurance
- Disability insurance
Quick Apply
Associate Business Development Director - Clinical Technology Sales
IQVIA —Wayne, NJ
- $89,600 - $249,600 a year
- Full-time
- Remote
- Microsoft Excel
- 3 years
- Analysis skills
- Work from home
Principal Data Manager I
Everest Clinical Research —Bridgewater, NJ
- $130,000 - $165,000 a year
- Remote
- Bachelor of Science
- Bachelor's degree
- Training & development
- AD&D insurance
- Disability insurance
Quick Apply

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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.

Quick Apply

Refine Your Search

clinical research associate remote jobs in new jersey

Clinical Research Associate- West Coast

Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)

Coordinator / Senior Coordinator, Project Services - Laboratories (Remote - East Coast)

Job Posting Title Clinical Trial Psych Rater - Italian Speaking

Clinical Program Manager

Associate Director, Clinical Data Management

Sr Project Specialist (Sponsor Dedicated/Remote)

Clinical Project Manager - Oncology (Client Dedicated/Remote)

Head of Clinical Data Management

Sr. Clinical Project Manager, IQVIA Biotech

Clinical Scientist - Ophthalmology

Clinical Scientist - Cardiovascular

Manager, Clinical Trial Management

Senior Clinical Trial Manager

Clinical Scientist - Immunology (Expertise in Ulcerative Colitis, Crohn’s disease and Rheumatology + Excel) - Clinical Drug Trial Exp - Must Have

Clinical Trial Manager - Full Service

Associate Director Radiopharmaceutical Clinical Applications – Mid-Atlantic (NJ, PA, Washington DC, MD, DE)

Clinical Database Designer I

Associate Business Development Director - Clinical Technology Sales

Principal Data Manager I

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