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Senior Clinical Data Manager Jobs (NOW HIRING)

ProPharma Group

$70 - $110/hr

## Sr. Clinical Data CoordinatorApplylocations: United Statestime type: Full timeposted on: Posted ... Perform ongoing updates of Data Management-related documentation, as needed.**Minimum Requirements*

Pantherx Specialty LLC

Clinical Data Manager

Robinson, PA · On-site

$110 - $150/hr

Senior Clinical Account Manager Purpose: The Clinical Data Manager develops and manages the data spec development during the implementation phase of a new product launch. This role works cross ...

asrcfh

Clinical Data Manager 3

San Antonio, TX · On-site

Agile Decision Sciences LLC is looking for a Clinical Data Manager 3 to support the growing team Responsibilities : * Manage the delivery of high-quality data from project start-up and planning to ...

Agilent

The Clinical Data Manager will plan and oversee all data management activities across assigned studies relatedcompaniondiagnostics (CDx) development to ensuretimely,accurate, and compliant data ...

Worldwide Clinical Trials

Clinical Data Manager

Join us! Clinical Data Manager does at Worldwide Oversee, lead, manage, and provide technicalexpertisewithin the assigned projects to ensure that they are executed in an efficient,accurate ...

CareMore Health

$130 - $195/hr

## Senior Clinical Data AnalystApplylocations: California, USAtime type: Full timeposted on: Posted 2 ... disease management.* Reporting & Visualization + Build and maintain dashboards, reports, and ...

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Senior Clinical Data Manager information

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$79K

$123.1K

$184.5K

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

As of Sep 6, 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.

Sr. Clinical Data Coordinator

ProPharma Group

On-site

$70 - $110/hr

Other

Posted 5 days ago

Key responsibilities

  • Perform ongoing data review, including reconciliation of third party data streams and serious adverse event reconciliation with the safety database.

  • Perform User Acceptance Testing (UAT) of clinical databases.

  • Perform Quality Control (QC) of clinical databases.

Job description

## 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 wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.**Title: Senior Clinical Data Coordinator** **FSP/Contractor** **Job Summary**The Sr. Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.**Summary of the Essential Functions of the Job*** Perform ongoing data review, including reconciliation of third party data streams and serious adverse event reconciliation with the safety database.* Perform User Acceptance Testing (UAT) of clinical databases.* Perform Quality Control (QC) of clinical databases.* Perform ongoing updates of Data Management-related documentation, as needed.**Minimum Requirements*** Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered.* Minimum of 3 years of data management experience is required.* Experience with Electronic Data Capture (EDC) system(s) is required.* Experience with Oracle Inc.'s InformTM EDC system is preferred.* Oncology and/or inflammatory therapeutic area experience is preferred.#LI-REMOTE#LI-AP1We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.\*\*\*ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.\*\*\* #J-18808-Ljbffr

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