ZipRecruiter

Log In

1

Contract Clinical Data Manager Jobs in New York, NY

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location ... Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract ...

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location ... Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract ...

IQVIA

Lead Clinical Data Manager (Remote)

New York, NY · Remote

$68.50K - $217.10K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for ...

IQVIA

Lead Clinical Data Manager (Remote)

Jersey City, NJ · Remote

$68.50K - $217.10K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for ...

IQVIA

Lead Clinical Data Manager (Remote)

Jersey City, NJ · Remote

$68.50K - $217.10K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for ...

IQVIA

Lead Clinical Data Manager (Remote)

New York, NY · Remote

$68.50K - $217.10K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for ...

next page

Showing results 1-20

People also search for

All JobsContract Clinical Data Manager JobsContract Clinical Data Manager Jobs in New York, NY

Contract Clinical Data Manager information

See New York, NY salary details

$21

$62

$89

How much do contract clinical data manager jobs pay per hour?

As of May 27, 2026, the average hourly pay for contract clinical data manager in New York, NY is $62.54, according to ZipRecruiter salary data. Most workers in this role earn between $49.42 and $74.42 per hour, depending on experience, location, and employer.

What is a Contract Clinical Data Manager job?

A Contract Clinical Data Manager is a temporary or freelance professional responsible for overseeing and managing clinical trial data for pharmaceutical, biotech, or CRO companies. They ensure data integrity, compliance with regulatory standards, and support database design, data cleaning, and reporting. Contract roles offer flexibility and typically involve working on specific projects or trials for a set duration.

What are the key skills and qualifications needed to thrive in the Contract Clinical Data Manager position, and why are they important?

To thrive as a Contract Clinical Data Manager, you need strong expertise in clinical data management, a background in life sciences, and familiarity with regulatory guidelines such as FDA or ICH-GCP. Proficiency in database systems like Medidata Rave or Oracle Clinical, coupled with knowledge of CDISC standards and, in many cases, a CCDM certification, is highly valued. Excellent attention to detail, strong organizational skills, and effective communication help distinguish top performers in this role. These abilities are crucial for ensuring compliant, high-quality data that supports successful clinical trials on a contractual or project basis.

What does a typical day look like for a Contract Clinical Data Manager?

A Contract Clinical Data Manager typically spends their days overseeing data collection, validation, and entry processes, ensuring that clinical trial data meets quality and regulatory standards. This role often involves close collaboration with data entry teams, biostatisticians, and clinical project managers to resolve discrepancies and maintain data integrity. Daily responsibilities may include designing case report forms, conducting data reviews, managing database queries, and preparing data for interim or final analyses. Working on a contract basis, you may manage multiple projects concurrently and must be adaptable to varying timelines and sponsor requirements.
More about Contract Clinical Data Manager jobs
What are the most commonly searched types of Clinical Data Manager jobs in New York, NY? The most popular types of Clinical Data Manager jobs in New York, NY are:
What are popular job titles related to Contract Clinical Data Manager jobs in New York, NY? For Contract Clinical Data Manager jobs in New York, NY, the most frequently searched job titles are:
What job categories do people searching Contract Clinical Data Manager jobs in New York, NY look for? The top searched job categories for Contract Clinical Data Manager jobs in New York, NY are:
Contract Clinical Data Manager jobs near you
Clinical Data Manager

Clinical Data Manager

Pharmaron

Somerset, NJ • On-site

$60K - $75K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday

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 .
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-JF1

Apply