Clinical Data Manager
Company: Pharmaron
Location: Somerset
Posted on: February 17, 2026
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Job Description:
Job Description Job Description Position: Clinical Data Manager
FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary:
$60,000 - $75,000 Pharmaron is a global CRO (Contract Research
Organization) helping pharma and biotech companies bring new
therapies to life. With over 21,000 employees worldwide across 23
locations in the US, UK and China, we support drug discovery
through to manufacturing with fully integrated, high-quality
services. We're proud of the impact we make and just last year, we
supported over 780 discovery projects , 1,000 CMC programmes , and
1,000 clinical trials across all phases. Our teams are involved in
everything from small molecules, ADC's, biologics, and gene
therapies and we work with more than 3,000 global customers . To
learn more, visit www.pharmaron.com. Job Overview: The Clinical
Data Manager ensures the integrity, accuracy, and compliance of
clinical trial data, adhering to regulatory requirements, SOPs, and
data standards. Responsibilities include overseeing data quality,
managing external data transfers, and ensuring database development
follows CDISC or relevant standards. They lead study management
activities, allocate resources, create timelines, and oversee data
management tasks. Additionally, they participate in audits,
communicate with stakeholders, assess risks, mentor junior staff,
and lead project teams to ensure high-quality data management
services aligned with client expectations. Responsibilities:
Responsible for ensuring the integrity, reliability, and accuracy
of clinical trial data. Ensure that clinical data quality and
consistency conform to applicable regulatory requirements, SOP(s),
processes, and data standards. Ensure that external data conforms
to standards outlined in the data transfer specification. Ensure
all data management activities are compliant with GCP, relevant
regulatory requirements, and SOP(s) of Pharmaron Clinical and/or
Sponsor. Ensure that data/database programming and development
follow and apply CDISC or applicable standards throughout the
duration of a clinical trial. Act as the Lead Data Manager for
clinical trials, arrange for resources and assess their workload. ?
Identify the work scope of the study and create a study timeline
based on the clinical protocol. Participate in internal/external
functional meetings. Oversight of all data management tasks related
to a clinical trial as mandated by the scope of work. Monitor the
project and ensure trial deliverables meet expected timelines and
quality standards. Participate in internal/external audits and
regulatory inspections. Provide risk management assessments for
data management deliverables. Lead clinical data management project
teams in the delivery of services to clients to ensure the provided
service is consistent with client needs, expectations, and
contractual obligations. What We're Looking For: Bachelor's Degree
or above in clinical/pharmacy, science and technology, or related
discipline preferred. At least 3 years' experience within a data
management role, understanding of processes including study
management, vendor management, CRF design, database set-up, edit
check specification, DMPs, and data cleaning activities up to and
including database lock. Demonstrated knowledge of GCP and other
regulatory requirements for clinical trials. Demonstrated knowledge
of the functions and activities of clinical trials. Why Pharmaron?
Pharmaron is a premier service provider for the life sciences
industry. Founded in 2004, Pharmaron has invested in its people and
facilities and established a broad spectrum of research,
development, and manufacturing service capabilities throughout the
entire drug discovery, preclinical, and clinical development
process across multiple therapeutic modalities, including small
molecules, biologics, and CGT products. With over 21,000 employees
and operations in the U.S., the U.K. and China. Pharmaron has an
excellent track record in delivering R&D solutions to its
partners in North America, Europe, Japan, and China. Collaborative
Culture: You will thrive in our inclusive and collaborative
environment, where teamwork and innovation go hand in hand. Here,
your voice matters, and your contributions make a real impact.
"Employees Number One" and "Clients Centered" are the core cultural
values at Pharmaron. Our culture, which sets Pharmaron apart from
other organizations, has evolved from our deep commitment to our
employees, partners, and collaborators. Benefits: As part of our
commitment to your well-being, we offer a comprehensive benefits
package: Insurance including Medical, Dental & Vision with
significant employer contributions Employer-funded Health
Reimbursement Account Healthcare & Dependent Care Flexible Spending
Accounts 100% Employer-paid Employee Life and AD&D Insurance,
Short- and Long-Term Disability Insurance 401k plan with generous
employer match Access to an Employee Assistance Program How to
Apply: Ready to seize this incredible opportunity? Join us at
Pharmaron and be part of a dynamic team driving innovation and
excellence in biopharmaceutical research and development. Apply
online today! As an Equal Employment Opportunity and Affirmative
Action employer, Pharmaron values diversity and inclusion in the
workplace, fostering an environment where all individuals are
empowered to succeed. Join us in our mission to make a difference
in the world of life sciences. LI-JB1
Keywords: Pharmaron, West Orange , Clinical Data Manager, Science, Research & Development , Somerset, New Jersey
