ZipRecruiter

Log In

1

Senior Clinical Data Associate Jobs (NOW HIRING)

Clinovo

Sr Clinical Data Manager

Waltham, MA · On-site

The Senior Clinical Data Manager will be responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This individual will ...

Triwill Group

$110 - $140/hr

Our partner is looking for a Senior Clinical Data Manager based in United States. This role offers the opportunity to lead clinical data management activities across the full lifecycle of complex ...

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 ...

ProPharma Group

$70 - $110/hr

## Sr. Clinical Data CoordinatorApplylocations: United Statestime type: Full timeposted on: Posted Yesterdayjob requisition id: JR 10393For the past 25 years, ProPharma has improved the health and ...

CareMore Health

$130 - $195/hr

## Senior Clinical Data AnalystApplylocations: California, USAtime type: Full timeposted on: Posted 2 Days Agojob requisition id: M104549** Summary**CareMore Health is seeking a Senior Clinical Data ...

Eli Lilly and Company

Senior Clinical Data Manager

The Senior Clinical Data Manager will report to the Senior Director of Data Sciences and serve as a handson contributor supporting Centessa's clinical programs. This role is ideal for an experienced ...

New

Eli Lilly and Company

Senior Clinical Data Manager

The Senior Clinical Data Manager will report to the Senior Director of Data Sciences and serve as a handson contributor supporting Centessa's clinical programs. This role is ideal for an experienced ...

New

previous pagenext page

Showing results 21-40

All JobsClinical Data Associate JobsSenior Clinical Data Associate Jobs

Senior Clinical Data Associate information

See salary details

$39.5K

$58.9K

$73.5K

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

As of Sep 5, 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 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 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 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 cities are hiring for Senior Clinical Data Associate jobs?

Cities with the most Senior Clinical Data Associate job openings:

What are the most commonly searched types of Senior Clinical Data jobs?

The most popular types of Senior Clinical Data jobs are:

What states have the most Senior Clinical Data Associate jobs?

States with the most job openings for Senior Clinical Data Associate jobs include:

Senior Clinical Data Associate jobs near you

Sr Clinical Data Manager

Clinovo

Waltham, MA • On-site

Contractor

Posted 4 days ago

Job description

Position Overview
A clinical-stage biotechnology company is seeking an experienced Senior Clinical Data Manager Consultant to support its growing clinical development organization.
The Senior Clinical Data Manager will be responsible for the oversight, coordination, and execution of clinical data management activities across one or more clinical trials. This individual will play a key role in developing and executing clinical data strategies that support high-quality, regulatory-compliant data deliverables.
The ideal candidate will bring significant sponsor-side clinical data management and vendor/CRO oversight experience, along with strong hands-on expertise with Medidata Rave.
This is a senior-level position requiring the ability to independently manage complex data management activities, identify and resolve issues, and effectively collaborate with Clinical Operations, Biostatistics, Statistical Programming, and other cross-functional stakeholders.
Key Responsibilities
  • Lead Clinical Data Management activities across assigned clinical trials from study start-up through database lock.
  • Develop and oversee eCRFs, eCRF completion guidelines, Data Management Plans (DMPs), data review guidelines, edit check specifications, and other study-specific data management documentation.
  • Design, review, and finalize case report forms (CRFs) in collaboration with cross-functional team members.
  • Oversee the implementation and maintenance of study-specific clinical data management systems and processes.
  • Lead and oversee database development, validation, user acceptance testing (UAT), and go-live activities.
  • Develop and execute plans for the processing, review, and cleaning of clinical trial data within established timelines and budgets.
  • Monitor clinical data flow and ensure timely, accurate, and high-quality data availability for analysis.
  • Identify data quality issues and work with internal teams and external partners to drive timely resolution.
  • Provide strong sponsor oversight of CROs, data management vendors, and other external partners responsible for outsourced data management activities.
  • Establish and monitor vendor performance, timelines, deliverables, and data quality expectations.
  • Review clinical protocols and Statistical Analysis Plans (SAPs) to ensure alignment with data collection and management requirements.
  • Ensure clinical data management activities comply with applicable SOPs, ICH-GCP, regulatory requirements, and industry standards.
  • Represent Clinical Data Management in cross-functional study team meetings.
  • Communicate project status, risks, issues, and proposed resolutions to project teams and leadership.
  • Provide recommendations regarding clinical data management processes, systems, and study-specific challenges.
  • Contribute to the continued development and improvement of data management processes, standards, and tools.
  • Monitor study-related data management budgets and evaluate vendor change orders and potential cost overruns.
  • Support audits and regulatory inspections and contribute to corrective and preventive action (CAPA) activities when required.
  • Train and mentor junior team members and promote clinical data management best practices.
  • Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical, Regulatory, and other functional stakeholders.
Required Experience & Qualifications
  • Bachelor's degree in a scientific, clinical, life sciences, or related discipline.
  • Minimum of 10 years of clinical data management experience within the pharmaceutical, biotechnology, or CRO industry.
  • Strong sponsor-side experience, including direct oversight of CROs and external data management vendors.
  • Extensive experience leading Clinical Data Management activities across the full clinical trial lifecycle, from study start-up through database lock.
  • Strong Medidata Rave experience required.
  • Expert knowledge of Electronic Data Capture (EDC) systems; experience with platforms such as Medidata Rave and Veeva.
  • Significant experience with database design, development, validation, and user acceptance testing.
  • Strong understanding of CDISC standards, including CDASH and SDTM.
  • Strong knowledge of ICH-GCP, FDA requirements, and other applicable clinical trial regulations and guidelines.
  • Expert understanding of clinical trial processes, clinical data flow, data review, and data cleaning best practices.
  • Demonstrated experience managing CROs, vendors, and global clinical study teams.
  • Proven ability to lead data management activities for complex and/or global clinical trials.
  • Ability to independently identify and resolve complex data management and technical issues.
  • Strong project management, organizational, and prioritization skills.
  • Excellent written and verbal communication skills.
  • Ability to effectively influence cross-functional stakeholders and senior leadership.
  • Ability to manage multiple priorities and studies within a fast-paced clinical development environment.
Key Candidate Profile
The strongest candidates will combine deep clinical data management expertise with significant sponsor-side oversight experience. Candidates should be comfortable operating independently, managing CRO and vendor deliverables, and serving as the Clinical Data Management subject matter expert within a cross-functional study team.
Medidata Rave expertise and strong sponsor oversight experience are critical requirements for this position.

Apply