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Senior Clinical Data Manager Jobs (NOW HIRING)

Ocugen Inc

Senior Clinical Data Manager

Malvern, PA · On-site

Position Summary The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data ...

Artivion

Sr. Clinical Data Manager

Kennesaw, GA

The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This ...

CryoLife

Sr. Clinical Data Manager

Kennesaw, GA · On-site

The Sr. Clinical Data Manager is responsible for data management operations and for the organization, coordination and execution of data management activities for assigned studies and projects. This ...

Allen Spolden

Senior Clinical Data Manager

Escondido, CA · On-site

... Clinical Data Manager manages the general conduct of project assigned tasks as the Lead Data Manager or under advisement from senior members of the Data Management Team. Responsible for oversight and ...

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Fortrea

Senior Clinical Data Manager

Durham, NC · On-site

The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and training to DM to ensure best working practices are maintained. Summary of Responsibilities:

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Senior Clinical Data Manager information

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How much do senior clinical data manager jobs pay per year?

As of Sep 1, 2026, the average yearly pay for senior clinical data manager in the United States is $123,055.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,500.00 and $137,500.00 per year, depending on experience, location, and employer.

What does a senior clinical data manager do?

A Senior Clinical Data Manager oversees the collection, validation, and management of clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They design and implement data management plans, coordinate with clinical teams, monitor data quality, and resolve discrepancies. In addition, they may lead data management teams and play a key role in preparing data for statistical analysis and regulatory submissions. Their work is crucial for supporting clinical research and ensuring reliable study results.

How does a senior clinical data manager typically collaborate with cross-functional teams during a clinical trial?

As a Senior Clinical Data Manager, you will work closely with clinical operations, biostatistics, medical writers, and regulatory teams throughout the lifecycle of a clinical trial. Your responsibilities often include coordinating data collection processes, ensuring data integrity, and resolving discrepancies by communicating with site monitors and data entry staff. Regular meetings and updates are common to align on data review timelines, discuss protocol amendments, and address any data-related issues swiftly. This high level of collaboration helps ensure that the clinical trial runs smoothly and meets regulatory standards.

What are the key skills and qualifications needed to thrive as a senior clinical data manager, and why are they important?

To thrive as a Senior Clinical Data Manager, you need a solid background in clinical research, data management practices, and a relevant degree such as life sciences or computer science. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) platforms, and knowledge of regulatory guidelines like GCP are essential, along with certifications such as CCDM. Strong leadership, analytical thinking, attention to detail, and excellent communication skills set top performers apart in this role. These skills ensure data integrity, regulatory compliance, and effective collaboration across cross-functional clinical teams, which are critical to the success of clinical trials.

What is the difference between Senior Clinical Data Manager vs Clinical Data Coordinator?

AspectSenior Clinical Data ManagerClinical Data Coordinator
CredentialsBachelor's/Master's in Life Sciences, Biostatistics, or related field; experience in data managementBachelor's degree in Life Sciences or related field; entry-level experience
Work EnvironmentLeads data management teams, oversees data quality, and ensures complianceSupports data entry, validation, and basic data queries
Industry UsageUsed in pharmaceutical, biotech, and clinical research organizationsCommon in clinical trial sites and research organizations

The Senior Clinical Data Manager typically has more experience, oversees data management processes, and ensures data quality, while the Clinical Data Coordinator handles data entry and validation tasks. Both roles are essential in clinical research but differ in responsibility level and scope.

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Senior Clinical Data Manager jobs near you
Infographic showing various Senior Clinical Data Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $123,055 per year, or $59.2 per hour.

Senior Clinical Data Manager

Malvern, PA • On-site

Ocugen Inc
Biotechnology Research and Development • 51 - 200 employees
Learn more about Ocugen Incexternal

Other

Posted 26 days ago

Job description

Position Summary
The Senior Clinical Data Manager plays a pivotal role within Ocugen's clinical data management team. This individual will lead data management efforts, oversee quality data collection and management processes, and contribute to critical aspects of clinical trial data handling, including database design, CRF development, data monitoring, and validation for clinical development programs and marketed products. In addition to technical responsibilities, the Senior Clinical Data Manager will provide leadership to junior data management staff and work collaboratively across functional teams, ensuring high-quality and timely deliverables.
Responsibilities
  • Oversee studies or a program, ensures cross study consistency, mentors team members, and manage vendors as needed.
  • Makes higher level decisions on data standards, risk based data management strategies, and protocol driven design choices.
  • Leads inspection readiness, ensures documentation completeness across studies,
  • Serves as a subject matter expert during audits, helps standardize SOP alignment, guides the team in applying GCP, ICH, CDISC, and internal compliance expectations.
  • Provides strategic input to Clinical Operations, Biostatistics, Programming, and Quality on data flow, database design improvements, standards adoption, and process optimizations.
  • Represents DM in program level meetings and drives improvements across studies (aligned with broader responsibilities seen in senior and principal level descriptions).
  • Provide mentorship and technical guidance to junior data management staff.
  • Ensure accurate and efficient collection of electronic clinical trial data.
  • Develop and validate edit checks and validation reports to maintain the highest quality data.
  • Ensure all required documentation is completed accurately and promptly across studies.
  • Develop and implement innovative data strategies to streamline data management workflows.
  • Identify and mitigate risks in data management processes proactively.
  • Take the lead on special projects and additional tasks as required by management.
  • Lead the development and execution of data management plans (DMPs), ensuring seamless data flow from collection to final analysis.
  • Design and oversee program standards and study-specific electronic Case Report Forms (eCRFs).
  • Partner with Biometrics, Clinical, and Regulatory teams to implement research protocols and ensure proper clinical data outputs for deliverables.
  • Develop and manage data transfer specifications, data review plans, and risk management strategies.
  • Collaborate on cross-functional project timelines and ensure database deliverables are achieved within schedule and quality standards.
  • Author and revise standard operating procedures (SOPs) and study-specific DMPs.
  • Prepare for and participate in audits, ensuring data management processes meet compliance standards.

  • BS degree in clinical, biological or mathematical sciences, or related field, or nursing qualification, or work- related equivalent.
  • 5-7 years of clinical data management experience in biopharma or CRO environment.
  • Strong attention to detail and motivation to provide quality deliverables.
  • Able to work in a fast-paced environment.
  • Experience with clinical trials.
  • Experience with CRFs, and in the development process of EDC databases, IRT systems and diary applications for data collection. Veeva experience is preferred.
  • Strong knowledge of GCPs, ICH, FDA, and CDISC regulatory requirements governing clinical studies.
  • Demonstrated attention to detail and outstanding organization skills.
  • Self-motivated with a commitment to high quality, on-time deliverables.
  • Excellent communication and collaboration skills with a team-oriented approach.
  • Demonstrated ability to identify and resolve issues and effectively manage timelines.

Working Conditions
This position operates in an office setting, in person. Remote work will be limited. Job may additionally require incumbent to be available outside of these hours to handle priority business needs.
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About Ocugen

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

51 - 200 Employees

Headquarters location

Malvern, PA, US

Year founded

2013

Social media

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