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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 ...

Fortrea

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:

Fortrea

Sr. Clinical Data Manager

Durham, CA · On-site

$120K/yr

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:

Fortrea

Sr. 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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How much do sr clinical data manager jobs pay per year?

As of Aug 16, 2026, the average yearly pay for sr 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 are the key skills and qualifications needed to thrive as a Sr Clinical Data Manager?

To thrive as a Sr Clinical Data Manager, you need expertise in clinical data management, knowledge of regulatory requirements (such as GCP and FDA), and typically a degree in life sciences or related fields. Proficiency with data management systems like Medidata Rave, Oracle Clinical, and experience with CDISC standards or relevant certifications are commonly required. Strong project management, leadership, and communication skills help you effectively oversee teams and ensure data quality. These skills and qualifications are crucial for ensuring accurate, compliant, and timely clinical trial data that supports successful regulatory submissions.

What does a Sr Clinical Data Manager do?

A Sr Clinical Data Manager oversees the collection, management, and quality control of clinical trial data. Their responsibilities include designing data collection systems, ensuring data accuracy and integrity, managing databases, and coordinating with clinical research teams. They play a critical role in ensuring that clinical data meets regulatory standards and is ready for analysis and submission. Typically, Sr Clinical Data Managers also mentor junior staff and help develop data management protocols and best practices.

What are some typical challenges a Sr Clinical Data Manager might face when overseeing multiple clinical trials simultaneously?

A Sr Clinical Data Manager often manages several trials at once, which can lead to challenges such as coordinating data collection across diverse study sites, ensuring consistent data quality, and meeting tight regulatory deadlines. Balancing these demands requires strong organizational skills, proactive communication with cross-functional teams, and effective delegation of tasks to junior data managers. Staying updated on evolving data standards and regulatory requirements is also crucial to avoid delays or compliance issues.
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Sr Clinical Data Manager jobs near you
Infographic showing various Sr Clinical Data Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 72% In-person, and 28% Remote job distribution, with an average salary of $123,055 per year, or $59.2 per hour.

Senior Clinical Data Manager

Ocugen Inc

Malvern, PA • On-site

Other

Posted 10 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

Twitter

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