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Associate Clinical Data Manager Jobs in Edison, NJ

The Sr. Manager Data Management is primarily responsible for the direct management of clinical study activities as they relate to data collection and processing from study start up through ongoing ...

The Sr. Manager Data Management is primarily responsible for the direct management of clinical study activities as they relate to data collection and processing from study start up through ongoing ...

Provide support for internal and external customers Manage work requests that describe particular ... data Continually increase subject matter knowledge on our products Interact with other teams to ...

Mgr, Database Management Systems Designs or modifies data models to solve complex database ... Essential Functions Clinical Data Standards & Operational Mapping * Participate in the development ...

Mgr, Database Management Systems Designs or modifies data models to solve complex database ... Essential Functions Clinical Data Standards & Operational Mapping * Participate in the development ...

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Associate Clinical Data Manager information

See Edison, NJ salary details

$14

$40

$89

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

As of Aug 11, 2026, the average hourly pay for associate clinical data manager in Edison, NJ is $40.33, according to ZipRecruiter salary data. Most workers in this role earn between $30.38 and $40.34 per hour, depending on experience, location, and employer.

What does an associate clinical data manager do?

An Associate Clinical Data Manager is responsible for collecting, cleaning, and managing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They work closely with clinical teams to design data collection tools, monitor data quality, and resolve discrepancies. Their work is crucial in supporting the analysis and reporting of clinical trial results, which can impact decisions about new medical treatments.

What are the key skills and qualifications needed to thrive as an associate clinical data manager?

To thrive as an Associate Clinical Data Manager, you need a solid background in life sciences or related fields, strong analytical abilities, and attention to detail, often supported by a relevant bachelor's degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools like Medidata Rave, and an understanding of regulatory guidelines such as ICH-GCP are typically required. Excellent organizational skills, effective communication, and problem-solving abilities help you excel in managing complex datasets and collaborating across teams. These skills ensure data integrity, regulatory compliance, and smooth conduct of clinical trials, which are critical to successful drug development.

What are some common challenges an associate clinical data manager might face when working on multi-site clinical trials?

Associate Clinical Data Managers often encounter challenges such as ensuring data consistency across different trial sites and managing discrepancies that arise from varying data entry practices. Coordinating with site staff, monitoring data quality, and adhering to strict timelines require strong communication and organizational skills. Additionally, adapting to evolving regulatory requirements and new data management technologies can be demanding, but these challenges also offer valuable learning opportunities for career growth.
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Infographic showing various Associate Clinical Data Manager job openings in Edison, NJ as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 92% Physical, 4% Hybrid, and 4% Remote job distribution, with an average salary of $83,876 per year, or $40.3 per hour.

Senior Manager, Data Management

Eisai

Nutley, NJ • Hybrid

$134K - $176K/yr

Full-time

Re-posted 24 days ago


Job description

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you.

The Sr. Manager Data Management is primarily responsible for the direct management of clinical study activities as they relate to data collection and processing from study start up through ongoing oversight to completion. Working in a highly matrixed environment, the successful candidate must have proven ability to effectively manage outsourced vendor activities as well as internal resources. The candidate must be capable of managing and leading others, providing appropriate feedback when warranted, setting clear direction for team members and appropriately assigning resources to meet work objectives. This individual may also act as "compound lead" for select projects to ensure consistency in the DB build across all protocols, ensuring conformity to Eisai standards.

Responsibilities:

  • Develop and review standard Case Report Forms (eCRFs), Data Management Plan, Validation Specifications and Data transfer Specifications.
  • Provide Data Management inputs during study protocol development; contribute to the enhancement of a clinical library.
  • Participate in the development/maintenance of DM SOPs, Standard Working Practices, and other data management related process documents as needed.
  • As appropriate, contribute to the selection, oversight of CRO performance related to Data Management activities; act as the sponsor representative for data management outsourced activities.
  • Represent the Data Management function in study teams meetings.
  • Ensure timely delivery of quality data in accordance with Eisai's SOP, industry standards, and regulatory guidelines.
  • Work closely with cross functional teams to ensure delivery of quality data; represent Data Management team in study team meetings and provide Data Management questions to internal and external team members.
  • Execute managerial duties to direct reports and/or provide guidance to members.


Qualifications:

  • Bachelors degree in sciences or related field with 7+ years of clinical data management experience in pharma/biotech industry OR a combination of equivalent education and experience.
  • Experience in project management (i.e. defining plans and milestones, coordinating with cross functional teams and driving accountabilities).
  • Experience working with clinical trials and the drug development process; understanding of Data Management strategy.
  • Experience leading data management activities in clinical trials.
  • Proficient use of data management systems with strong knowledge of data management processes, tools, methodologies and documentation.
  • Strong experience and knowledge of clinical research, GCP, regulatory requirements and good data management practices.
  • Some experience with line management; mentoring team members (external/contract staff) on clinical data management activities and procedures preferred.
  • Proven performance in earlier role.
  • Position is hybrid, requiring 3 days onsite per week in our Nutley, NJ office (Tuesday, Wednesday and Thursday).

#LI-MI1

Skills:Communication & Cross-functional Influence, Critical Thinking & Business Agility, Data Management Knowledge/Skills, Industry/ Regulatory Knowledge, Mentoring/ People Development, Project Management, Vendor Management

Eisai Salary Transparency Language:

The annual base salary range for the Senior Manager, Data Management is from :$134,800-$176,900Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan.

Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills.

Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit https://careers.eisai.com/us/en/compensation-and-benefits.

Certain other benefits may be available for this position, please discuss any questions with your recruiter.

Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans.

Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information:

Right To Work

E-Verify Participation


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About Eisai

Sourced by ZipRecruiter

Eisai is a global pharmaceutical company (headquartered in Woodcliff Lake, NJ, US), renowned for its innovative research and development in neuroscience and oncology. The primary focus of the company is to provide therapeutic treatments and solutions for diseases like Alzheimer's, cancer, and other neurological disorders. Eisai was founded in Japan in 1941 and has since developed a strong presence across international markets. Eisai's core values center around their philosophy of 'human health care' (hhc), where they aim to make significant and positive contributions to patients and their families' healthcare worldwide.

Company size

1,001 - 5,000 Employees

Headquarters location

Nutley, NJ, US

Year founded

1995

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