Clinical Trial Manager Jobs in New Jersey
Clinical Trial Manager jobs in New Jersey are among the most active in the country, concentrated in pharmaceutical R&D, contract research organizations, and biotech, with openings at every level from entry-level clinical trial coordinator stepping up to senior director of clinical operations. The densest hiring clusters are in Princeton, Parsippany, and the Raritan Valley corridor, where companies like Johnson & Johnson, Merck, and Pfizer maintain deep clinical operations footprints. The most in-demand specialties are oncology trial management, Phase II through Phase IV oversight, and regulatory submissions experience. Find a role that fits below and apply directly.
Find Clinical Trial Manager JobsOverview
Showing 5 of 16+ Clinical Trial Manager jobs
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
JOB SUMMARY:
Performs administrative and support activities, as assigned by the Clinical Trial Supplies Manager (CTSM) or Project Lead (PL), to help manage the logistics of clinical trial supplies (e.g., batch review, customs clearance, supply and return). The Senior Clinical Trial Supplies Associate operates independently, with minimal day-to-day oversight, and may co-ordinate the activities of other Clinical Trial Supplies Associates.
JOB RESPONSIBILITIES:
Monitor clinical supply inventory levels, trends, and potential supply risks.
Support supply forecasting, metrics reporting, and inventory tracking activities.
Process requisitions and coordinate procurement of comparator drugs and ancillary supplies.
Coordinate clinical supply shipments, depot transfers, and site return logistics.
Track shipment delivery schedules and assist with temperature excursion investigations and resolution.
Maintain study documentation, including Expected Document Lists (EDLs), comparator records, and Electronic Trial Master File (eTMF) documentation.
Support QA/QP release requests, inspection readiness activities, and pack-and-label reconciliation processes.
Assist with Interactive Response Technology (IRT) activities, including user access management, alert monitoring, and User Acceptance Testing (UAT).
Conduct product compatibility research and maintain related data in approved databases and tracking tools.
Manage clinical supply system records, shared mailboxes, and documentation uploads within Veeva.
QUALIFICATION REQUIREMENTS:
- Bachelor’s Degree (or equivalent) level of education, preferably in a related field or focused on life sciences
- Moderate experience (2+ years) in a contract research organization (CRO), pharmaceutical, or biotechnology company
- Strong k now l e d ge of G ood C l i n i c a l P r a c t i c e, ICH g u i d e l i nes, Good Manufacturing Practice, a nd other a p p li c a b l e r eg u l a t o r y r equ i r e m ents
- High l e v e l of c o m peten c e i n E n g l i s h l a n gu a ge
- Ability to perform several tasks simultaneously to meet deadlines
- Self-motivation and ability to work independently
- High p r o f i c i e n c y w i th M S O ff i c e A pp l i c a t i on s
- A b i l i t y to t r a v e l as ne c e ss a r y (up to 10%)
At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.
Salary Range:
$56,400.00 - $95,900.00The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.
Discover what your 25,000 future colleagues already know:
Why Syneos Health
- We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
- We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
- We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.
Job Responsibilities
JOB SUMMARY:
Performs administrative and support activities, as assigned by the Clinical Trial Supplies Manager (CTSM) or Project Lead (PL), to help manage the logistics of clinical trial supplies (e.g., batch review, customs clearance, supply and return). The Senior Clinical Trial Supplies Associate operates independently, with minimal day-to-day oversight, and may co-ordinate the activities of other Clinical Trial Supplies Associates.
JOB RESPONSIBILITIES:
Monitor clinical supply inventory levels, trends, and potential supply risks.
Support supply forecasting, metrics reporting, and inventory tracking activities.
Process requisitions and coordinate procurement of comparator drugs and ancillary supplies.
Coordinate clinical supply shipments, depot transfers, and site return logistics.
Track shipment delivery schedules and assist with temperature excursion investigations and resolution.
Maintain study documentation, including Expected Document Lists (EDLs), comparator records, and Electronic Trial Master File (eTMF) documentation.
Support QA/QP release requests, inspection readiness activities, and pack-and-label reconciliation processes.
Assist with Interactive Response Technology (IRT) activities, including user access management, alert monitoring, and User Acceptance Testing (UAT).
Conduct product compatibility research and maintain related data in approved databases and tracking tools.
Manage clinical supply system records, shared mailboxes, and documentation uploads within Veeva.
QUALIFICATION REQUIREMENTS:
- Bachelor’s Degree (or equivalent) level of education, preferably in a related field or focused on life sciences
- Moderate experience (2+ years) in a contract research organization (CRO), pharmaceutical, or biotechnology company
- Strong k now l e d ge of G ood C l i n i c a l P r a c t i c e, ICH g u i d e l i nes, Good Manufacturing Practice, a nd other a p p li c a b l e r eg u l a t o r y r equ i r e m ents
- High l e v e l of c o m peten c e i n E n g l i s h l a n gu a ge
- Ability to perform several tasks simultaneously to meet deadlines
- Self-motivation and ability to work independently
- High p r o f i c i e n c y w i th M S O ff i c e A pp l i c a t i on s
- A b i l i t y to t r a v e l as ne c e ss a r y (up to 10%)
At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.
Salary Range:
$56,400.00 - $95,900.00The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
See All 16 Clinical Trial Manager Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Clinical Trial Manager JobsClinical Trial Manager Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Clinical Trial Manager Job Market in New Jersey
A snapshot from current New Jersey openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Medical Devices
- Science & Research
- Technology & Software
- Consulting & Professional Services
What New Jersey Employers Look For
The qualifications that appear most often in clinical trial manager jobs across New Jersey.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Minimum two to five years of direct clinical trial management or coordination experience
- Demonstrated knowledge of ICH-GCP guidelines and FDA regulatory requirements
- Experience with clinical trial management systems such as Medidata Rave or Veeva Vault
- Strong protocol adherence and site monitoring or oversight experience
- Project management skills with ability to manage multiple simultaneous study timelines
Clinical Trial Manager Jobs in New Jersey: Frequently Asked Questions
How do you become a clinical trial manager in New Jersey?
Most clinical trial managers in New Jersey enter the role through a bachelor's degree in a life science, nursing, or healthcare field, followed by experience as a clinical trial coordinator or research associate. New Jersey does not require a state-issued license specific to this role, but many employers prefer or require the Association of Clinical Research Professionals certification. Building experience at one of New Jersey's many CROs or pharmaceutical headquarters is the most direct path.
Which companies hire clinical trial managers in New Jersey?
Employers hiring clinical trial managers in New Jersey right now include IQVIA, Katalyst Healthcares & Life Sciences, and Genmab, based on current listings on Migrate Mate as of October 2026. New Jersey's concentration of major pharmaceutical headquarters and contract research organizations makes it one of the most consistently active states for this role year-round.
Which New Jersey cities have the most clinical trial manager jobs?
The cities with the most clinical trial manager openings in New Jersey are Edison, Gladstone, and Princeton. This distribution reflects the state's pharmaceutical and biotech corridor, anchored by major corporate campuses and CRO offices concentrated along the Route 1 and I-287 corridors, with Princeton and Parsippany drawing the largest share of clinical operations hiring.
Are there remote clinical trial manager jobs in New Jersey?
Yes, and more than many clinical roles, since a meaningful portion of trial oversight, vendor management, and data review can be done off-site. About 89% of clinical trial manager openings tied to New Jersey are remote or hybrid as of October 2026, with fully remote roles most common in late-phase or post-market study oversight positions that do not require regular site visits.
How can I get hired as a clinical trial manager in New Jersey with little or no experience?
The most realistic entry path is starting as a clinical trial coordinator or clinical research associate at one of New Jersey's CROs or pharmaceutical companies, then moving into management after demonstrating protocol and site oversight competency. Large New Jersey employers like major pharma companies and CROs regularly post coordinator-level roles that serve as direct pipelines to manager positions. Earning an ACRP certification early signals seriousness to New Jersey hiring teams and gives a clear credential edge before the experience base is deep.
Where can I find and apply to clinical trial manager jobs in New Jersey?
You can find and apply to clinical trial manager jobs in New Jersey on Migrate Mate, which lists current New Jersey openings from employers across the state. Find roles that fit your experience and apply directly to the ones that match.
See All 16 Clinical Trial Manager Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
Find Clinical Trial Manager Jobs