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Senior Clinical Data Associate 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 ...

Celldex Therapeutics

Senior Clinical Data Manager

New Haven, CT · On-site

$133K - $173K/yr

  • Medical

  • Retirement

  • PTO

Overview The Senior Clinical Data Manager is responsible for managing the data management activities for multiple clinical trials. Will work closely with internal team members and vendors to ensure ...

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 ...

ImmunityBio, Inc.

Senior Clinical Data Manager

Dunkirk, NY · On-site

$140K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position Summary The Senior Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to ...

ImmunityBio, Inc.

Senior Clinical Data Manager

Dunkirk, NY · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position Summary The Senior Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to ...

NKW NantKwest Inc

Senior Clinical Data Manager

Dunkirk, NY

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position Summary The Senior Clinical Data Manager is an expert in clinical data management with demonstrated capability in building and maintaining clinical trial databases. They contribute to ...

Unlearn.AI

Senior Clinical Data Scientist

San Francisco, CA · On-site

$180 - $240/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Senior Clinical Data Scientists at Unlearn build world-class data products that underpin advances in machine learning for clinical research. Working in close collaboration with machine learning ...

Unlearn

Senior Clinical Data Scientist

San Francisco, CA · On-site

$160 - $210/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Senior Clinical Data Scientists at Unlearn build world-class data products that underpin advances in machine learning for clinical research. Working in close collaboration with machine learning ...

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Senior Clinical Data Associate information

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

As of Aug 15, 2026, the average yearly pay for senior clinical data associate in the United States is $58,937.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,000.00 and $67,500.00 per year, depending on experience, location, and employer.

What are some common challenges senior clinical data associates face when managing large clinical trial datasets?

Senior Clinical Data Associates often manage complex datasets from multiple sites, which can lead to challenges such as ensuring data consistency across sources, resolving discrepancies, and maintaining data integrity under tight timelines. Additionally, they must stay up-to-date with evolving regulatory requirements and work closely with cross-functional teams, including biostatisticians, clinical operations, and data managers, to ensure accurate and timely data delivery. Effective communication, attention to detail, and adaptability are essential to overcome these challenges and ensure successful trial outcomes.

What are the key skills and qualifications needed to thrive as a senior clinical data associate?

To thrive as a Senior Clinical Data Associate, you need expertise in clinical data management, data cleaning, and knowledge of clinical trial processes, supported by a degree in life sciences or a related field. Familiarity with data management systems like Medidata Rave, EDC platforms, and certifications such as CCDM are commonly required. Attention to detail, strong analytical thinking, and effective communication skills help you excel in ensuring data accuracy and collaborating with cross-functional teams. These capabilities are crucial for maintaining data integrity, regulatory compliance, and the overall success of clinical research studies.

What does a senior clinical data associate do?

A Senior Clinical Data Associate is responsible for managing and ensuring the accuracy, integrity, and quality of data collected during clinical trials. They oversee data collection processes, review case report forms, resolve data discrepancies, and ensure compliance with regulatory standards. In addition to performing data management tasks, Senior Clinical Data Associates often mentor junior staff, contribute to developing data management plans, and collaborate with clinical research teams to ensure successful trial outcomes.

What cities are hiring for Senior Clinical Data Associate jobs?

Cities with the most Senior Clinical Data Associate job openings:

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Senior Clinical Data Associate jobs near you

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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