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Sr 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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Sr Clinical Data Manager information

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$79K

$123.1K

$184.5K

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

As of Sep 5, 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 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 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 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 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 4 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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