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Contract Senior Clinical Research Associate Jobs in Basking Ridge, NJ

Legend Biotech US

Senior Clinical Trial Associate

Somerset, NJ · On-site

$35.50 - $48.25/hr

Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural ... Legend Biotech is seeking a Senior Clinical Trial Associate as part of the Clinical Operations team ...

Excel Gens

Sr. Clinical Research Coordinator

Manhattan, NY

$26.75 - $35.50/hr

Clinical Research Analyst Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Develops work flow policies and ...

Excel Gens

Sr. Clinical Research Coordinator

Manhattan, NY

$26.75 - $35.50/hr

Clinical Research Analyst Under general supervision, analyzes and interprets highly complex clinical research data; conducts clinical testing and develops protocols. Develops work flow policies and ...

MSD

Senior Clinical Director, Hematology

Rahway, NJ · On-site

Participating in internal and joint internal/external research project teams relevant to the ... Associate Vice President in ensuring that appropriate personnel are informed of the progress of ...

IQVIA

Clinical Research Associate

Parsippany, NJ · On-site

$87K - $182K/yr

Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

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All JobsContract Clinical Research Associate JobsContract Senior Clinical Research Associate JobsContract Senior Clinical Research Associate Jobs in Basking Ridge, NJ

Contract Senior Clinical Research Associate information

See Basking Ridge, NJ salary details

$37.1K

$97.2K

$147.9K

How much do contract senior clinical research associate jobs pay per year?

As of Sep 7, 2026, the average yearly pay for contract senior clinical research associate in Basking Ridge, NJ is $97,196.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,400.00 and $131,900.00 per year, depending on experience, location, and employer.

What is a contract senior clinical research associate?

A Contract Senior Clinical Research Associate (CRA) is an experienced clinical research professional who works independently or through an agency on a contract basis, rather than as a permanent employee. Their primary role is to monitor clinical trials, ensuring that studies are conducted according to protocol, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Senior CRAs have advanced knowledge of clinical trial processes and often oversee multiple sites or junior staff. They are responsible for reviewing data, managing documentation, and acting as a liaison between the study sponsor and the investigative sites. Contract positions offer flexibility and variety, but may require more travel and self-management.

What skills and qualifications are needed to thrive as a contract senior clinical research associate?

To thrive as a Contract Senior Clinical Research Associate, you need comprehensive knowledge of clinical trial processes, GCP/ICH guidelines, and relevant regulatory requirements, typically supported by a life sciences degree and several years of monitoring experience. Familiarity with Electronic Data Capture (EDC) systems, trial management software, and certifications like ACRP or SOCRA are commonly required. Exceptional organizational skills, attention to detail, and effective communication make someone stand out in this role. These skills and qualities are vital to ensure protocol compliance, high data quality, and successful collaboration across study sites.

How does a contract senior clinical research associate typically collaborate with study sites and sponsors during a clinical trial?

As a Contract Senior Clinical Research Associate (CRA), you play a key liaison role between study sites and sponsors. You are responsible for monitoring site performance, ensuring protocol compliance, and addressing any issues that arise during the trial. Regular communication with site staff and sponsor representatives is essential, often involving site visits, remote monitoring, and reporting. Effective collaboration helps maintain study integrity, ensures regulatory requirements are met, and facilitates the timely progression of the clinical trial.

What is the difference between Contract Senior Clinical Research Associate vs Clinical Research Associate?

AspectContract Senior Clinical Research AssociateClinical Research Associate
CredentialsBachelor's degree, relevant certifications, experience in clinical trialsBachelor's degree, entry-level certifications often sufficient
Work EnvironmentContract basis, often in multiple sites or projects, possibly remoteFull-time or part-time, typically at a single site or sponsor location
Employer & Industry UsagePharmaceutical companies, CROs, biotech firms, project-basedPharmaceutical companies, CROs, hospitals, research sites

The Contract Senior Clinical Research Associate typically has more experience, handles complex trial aspects, and works on a contractual basis. The Clinical Research Associate is often an entry-level or mid-level role focused on site monitoring and data collection. Both roles are essential in clinical trials but differ mainly in experience level and employment type.

What are popular job titles related to Contract Senior Clinical Research Associate jobs in Basking Ridge, NJ?

For Contract Senior Clinical Research Associate jobs in Basking Ridge, NJ, the most frequently searched job titles are:

What cities near Basking Ridge, NJ are hiring for Contract Senior Clinical Research Associate jobs?

Cities near Basking Ridge, NJ with the most Contract Senior Clinical Research Associate job openings:

Contract Senior Clinical Research Associate jobs near you
Infographic showing various Contract Senior Clinical Research Associate job openings in Basking Ridge, NJ as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $97,196 per year, or $46.7 per hour.

Senior Clinical Research Coordinator - Oncology

Vitalief

Newark, NJ • On-site

$75K - $85K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 12 days ago

Job description

ABOUT VITALIEF
Vitalief is a consulting firm built exclusively for the research and clinical trial industry, providing innovative Consulting and Functional Service Provider (FSP) solutions to academic medical centers, health systems, sponsors, CROs, and site networks. By combining deep subject matter expertise with the experience of senior research practitioners, we help organizations accelerate study activation, optimize operations, improve financial performance, and build scalable workforce solutions that reduce costs, increase efficiency, and advance clinical breakthroughs for patients.
POSITION SUMMARY
Vitalief is seeking an experienced Senior Clinical Research Coordinator (CRC) to join our team as a full-time employee with a comprehensive benefits package. This role will support a portfolio of Phase II-IV oncology interventional clinical trials at a community hospital site in Newark, NJ.
The ideal candidate will have a minimum of three years of clinical research coordination experience, a strong background supporting oncology trials across multiple disease areas, experience mentoring junior CRC team members, and the ability to excel in a collaborative, small-team environment.
WHY VITALIEF?
  • Meaningful Impact: Support innovative oncology research that advances treatment options and improves patient outcomes.
  • People-First Culture: Join a collaborative environment focused on professional growth, innovation, and teamwork.
  • Comprehensive Benefits: Enjoy 20 PTO days, 9 paid holidays, company-paid life insurance, short- and long-term disability coverage, a 401(k) retirement plan, and comprehensive healthcare benefits.
  • Work Location: Fully on site in Newark, NJ for the first 3 months. Following training, transition to a hybrid schedule of 4 days onsite and 1 remote day per week.
  • Schedule: Monday through Friday, 8:00 AM - 4:30 PM.
  • Salary Range: $75,000 to $85,000 depending on experience.

RESPONSIBILITIES
  • Support the execution of Phase II-IV oncology clinical trials, including pharmaceutical-sponsored, ECOG, and investigator-initiated studies.
  • Manage trials across multiple oncology disease groups, including GYN, Breast, GI/GU, Head & Neck, and Lung cancers.
  • Oversee a portfolio of approximately 15-20 active clinical trials in a fast-paced, high-volume clinical environment.
  • Identify and screen potential study participants using physician schedules, pathology reports, multidisciplinary tumor boards, referrals, and other clinical resources.
  • Obtain informed consent and enroll eligible patients in accordance with protocol requirements and regulatory standards.
  • Manage patients throughout the clinical trial lifecycle, from consent through completion of active treatment.
  • Educate patients regarding study procedures, treatment schedules, and protocol requirements.
  • Coordinate patient care activities with physicians, infusion teams, nursing staff, radiology, pathology, laboratories, and other clinical departments.
  • Monitor patient safety, document clinical outcomes, and ensure timely reporting of adverse events and Serious Adverse Events (SAEs).
  • Maintain accurate clinical trial documentation, source records, regulatory files, patient calendars, and study-related documentation.
  • Ensure compliance with study protocols, Good Clinical Practice (GCP), institutional policies, and regulatory requirements.
  • Provide guidance and mentorship to junior CRC team members and support team collaboration.

QUALIFICATIONS
  • Bachelor's degree in health science, life science, nursing, or a related field.
  • Minimum of 3 years of clinical research coordination experience supporting interventional Phase II-IV clinical trials.
  • Required oncology clinical trial experience, preferably with exposure to multiple oncology disease areas.
  • Experience with patient identification, pre-screening, informed consent, enrollment, retention, regulatory compliance, and clinical data management.
  • Prior experience mentoring or supporting the development of junior CRCs.
  • Proficiency with EPIC and OnCore™ CTMS.
  • Ability to manage multiple concurrent studies while maintaining strong attention to detail and organization.
  • Adaptable, solutions-oriented mindset with the ability to work effectively in a small, collaborative team environment.
  • Strong interpersonal and communication skills with the ability to work closely with physicians, nurses, research staff, hospital departments, and external partners.
  • Experience ensuring SAEs are documented, completed, and reported within protocol-defined timelines.
  • Proficiency with Microsoft Office applications and clinical research systems.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing.
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.
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