Senior Clinical Trial Manager Jobs in New Jersey
Senior Clinical Trial Manager jobs in New Jersey are among the most active in the country, concentrated in the pharmaceutical, biotechnology, and medical device sectors that define the state's life sciences corridor. Most hiring is in and around Bridgewater, Parsippany, and Princeton, where companies like Johnson and Johnson, Merck, and Novartis maintain significant operations. The most consistent openings are in oncology, rare disease, and late-phase trials. Find a role that fits below and apply directly.
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Showing 5 of 16+ Senior 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 Senior Clinical Trial Manager Jobs in New Jersey
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Find JobsSenior Clinical Trial Manager Jobs by City in New Jersey
Where New Jersey roles are concentrated, by current openings.
Senior 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 senior clinical trial manager jobs across New Jersey.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Minimum five years of clinical trial management experience across multiple phases
- Demonstrated ability to manage CRO relationships and vendor oversight independently
- Proficiency with electronic data capture systems such as Medidata Rave or Veeva Vault
- Strong knowledge of ICH-GCP guidelines and FDA regulatory requirements for clinical trials
- PMP or ACRP CCRA certification preferred by many New Jersey pharmaceutical employers
Senior Clinical Trial Manager Jobs in New Jersey: Frequently Asked Questions
How do you become a senior clinical trial manager in New Jersey?
The path to a senior clinical trial manager role in New Jersey typically starts with a bachelor's degree in a life science, pharmacy, or nursing discipline, followed by several years of hands-on clinical operations experience. New Jersey does not require a state-issued license specific to this role, but many employers prefer candidates who hold certifications from the Association of Clinical Research Professionals or the Society of Clinical Research Associates. Building experience within the state's dense pharmaceutical corridor strengthens candidacy considerably.
Which companies hire senior clinical trial managers in New Jersey?
Employers hiring senior 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 global pharmaceutical and biotechnology headquarters means demand is consistent across both large sponsors and contract research organizations with offices in the state.
Which New Jersey cities have the most senior clinical trial manager jobs?
Edison, Gladstone, and Princeton account for the highest concentration of senior clinical trial manager openings in New Jersey. The Bridgewater and Parsippany areas anchor much of the hiring because of the large pharmaceutical headquarters clustered there, while Princeton draws openings tied to biotechnology research campuses and academic medical partnerships in the surrounding region.
Are there remote senior clinical trial manager jobs in New Jersey?
Yes, and more than most clinical roles, since senior clinical trial managers handle oversight, vendor management, and documentation work that translates well to remote settings. About 89% of senior clinical trial manager openings tied to New Jersey are remote or hybrid as of October 2026, reflecting the desk-heavy nature of the senior function. Protocol oversight, site communication, and regulatory writing are the responsibilities most commonly performed remotely.
How can I get hired as a senior clinical trial manager in New Jersey with little or no experience?
The most realistic entry path is through a clinical research associate or clinical trial associate role at one of the many contract research organizations operating in New Jersey, such as those with offices in Parsippany or Princeton. From there, candidates build site monitoring and protocol management experience before moving into managerial positions. Completing an ACRP or SOCRA certification early strengthens applications, and New Jersey's large pharmaceutical employers frequently post associate clinical trial manager openings that serve as a direct bridge to senior-level roles.
Where can I find and apply to senior clinical trial manager jobs in New Jersey?
You can find and apply to senior clinical trial manager jobs in New Jersey on Migrate Mate, which lists current openings in the state. Search the available roles, find the ones that match your experience and target companies, and apply directly to the employers posting them.
See All 16 Senior Clinical Trial Manager Jobs in New Jersey
Find roles in New Jersey that match your experience and apply in just a few clicks.
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