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Senior Clinical Data Scientist Jobs (NOW HIRING)

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

Experience in molecular and clinical data analysis. * Experience in searching through and understanding scientific and regulatory literature. * Experience in working independently in a fast-paced ...

DiaSorin

Clinical Data Scientist

Austin, TX · On-site

Experience in molecular and clinical data analysis. * Experience in searching through and understanding scientific and regulatory literature. * Experience in working independently in a fast-paced ...

ImmunityBio, Inc.

Senior Clinical Data Manager

Dunkirk, NY · On-site

$140K/yr

The Company is applying its science and platforms to treating cancers, including the development of ... Position Summary The Senior Clinical Data Manager is an expert in clinical data management with ...

Merck & Co.

The Senior Clinical Scientist provides scientific leadership for one or more clinical trials or key ... Clinical Data Review & Scientific Insights Lead ongoing review and interpretation of clinical data ...

New

MSD

Senior Clinical Scientist, Immunology

Rahway, NJ · On-site

The Senior Clinical Scientist provides scientific leadership for one or more clinical trials or key ... Clinical Data Review & Scientific Insights * Lead ongoing review and interpretation of clinical ...

MSD

Senior Clinical Scientist, Immunology

San Diego, CA · On-site

The Senior Clinical Scientist provides scientific leadership for one or more clinical trials or key ... Clinical Data Review & Scientific Insights * Lead ongoing review and interpretation of clinical ...

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Senior Clinical Data Scientist information

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$41.5K

$142.5K

$201K

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

As of Aug 17, 2026, the average yearly pay for senior clinical data scientist in the United States is $142,460.00, according to ZipRecruiter salary data. Most workers in this role earn between $118,500.00 and $166,500.00 per year, depending on experience, location, and employer.

What does a senior clinical data scientist do?

A Senior Clinical Data Scientist is responsible for managing, analyzing, and interpreting large sets of clinical trial data to support drug development and medical research. They design and implement data analysis strategies, ensure data quality, and collaborate with cross-functional teams such as statisticians, clinicians, and regulatory experts. Their goal is to generate insights that drive decision-making in the development of safe and effective therapies. Additionally, they may oversee junior data scientists and contribute to the development of data management protocols and best practices.

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

To thrive as a Senior Clinical Data Scientist, you need advanced expertise in biostatistics, data analysis, and clinical research, typically supported by a master’s or PhD in a quantitative field. Proficiency with statistical programming languages (such as SAS, R, or Python), clinical trial data management systems, and familiarity with regulatory standards like CDISC are essential. Strong problem-solving skills, attention to detail, and the ability to communicate complex data findings to diverse stakeholders make someone stand out in this position. These skills are crucial for ensuring the integrity, accuracy, and regulatory compliance of clinical data to support successful drug development and approval.

How does a senior clinical data scientist typically collaborate with cross-functional teams during a clinical trial?

A Senior Clinical Data Scientist works closely with biostatisticians, clinical operations, medical writers, and regulatory affairs teams throughout the lifecycle of a clinical trial. They are responsible for ensuring data integrity, developing statistical analysis plans, and interpreting complex datasets to support decision-making. Regular meetings and data review sessions are common, where the data scientist provides insights, addresses data-related challenges, and ensures that all stakeholders have the information they need to keep the trial on track. This collaborative environment is essential for maintaining compliance and achieving trial objectives efficiently.

What is the difference between Senior Clinical Data Scientist vs Clinical Data Scientist?

AspectSenior Clinical Data ScientistClinical Data Scientist
Required CredentialsAdvanced degree (Master's/PhD), experience in data analysis, statistical skillsSimilar credentials, often entry to mid-level experience
Work EnvironmentLeading projects, mentoring, strategic decision-makingData analysis, reporting, supporting project teams
Employer & Industry UsagePharmaceuticals, biotech, clinical research organizationsSame industries, typically at earlier career stages
Search & Comparison IntentUnderstanding senior-level roles, career progressionEntry to mid-level roles, skill development

The main difference between a Senior Clinical Data Scientist and a Clinical Data Scientist lies in experience, responsibilities, and leadership. Senior roles involve strategic decision-making, project leadership, and mentoring, while Clinical Data Scientists focus on data analysis and supporting research efforts. Both roles are vital in clinical research, but the senior position requires more experience and a broader scope of responsibilities.

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Senior Clinical Data Scientist jobs near you
Infographic showing various Senior Clinical Data Scientist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $142,460 per year, or $68.5 per hour.

Senior Clinical Data Manager

Worldwide Clinical Trials

Remote

Full-time

Posted 25 days ago

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What the Senior Clinical Data Manager does at Worldwide

Oversee, lead, manage, and provide technical expertise within assigned projects to ensure they are executed in an efficient, accurate, and timely manner to the Sponsor's satisfaction.

What you will do

  • Provide fully independent and autonomous leadership of data management services (start-up, conduct, and closeout) across multiple complex global projects/programs
  • Ensure appropriate resources are allocated to complete all data management (DM) activities on time and within budget
  • Prepare DM trial documentation, including Data Management Plans (DMPs), Database Specifications, Edit Check Specifications, CRF Completion Guidelines (CCGs), and Data Transfer Agreements (DTAs)
  • Ensure effective User Acceptance Testing (UAT) is performed
  • Write external vendor reconciliation specifications for programming reconciliation outputs (e.g., Serious Adverse Events, Interactive Response Technology (IRT), Central Laboratory)
  • Oversee data cleaning activities
  • Produce metrics to monitor progress of trial activities
  • Ensure all database lock activities are completed on time
  • Represent Worldwide Clinical Trials Data Management at both internal and external study meeting calls, including providing input
  • Monitor project scope, budgets, and risks and alert DM Management of any concerns
  • Liaise with DM Management at regular intervals to discuss progress and any outstanding issues (e.g., during Project Review Meetings)
  • Collaborate with internal Worldwide Clinical Trials departments working on the same project
  • Provide feedback on process improvements to DM Management and/or Subject Matter Experts (SMEs)
  • Participate in and lead process reviews
  • Provide training, support, and mentorship to other members of the DM department
  • Participate, as necessary, in sponsor audits, regulatory authority inspections, and other third-party meetings
  • Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

What you bring to the role

  • Excellent attention to detail
  • Excellent written and verbal communication skills
  • Strong knowledge of data management best practices and technologies as applied to clinical trials
  • Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams
  • Strong understanding of clinical trial processes, protocol documents (protocols, Statistical Analysis Plans (SAPs), Case Report Forms (CRFs), study reports), and related procedures
  • Strong analytical and problem-solving skills
  • Independent and autonomous project oversight skills

Your experience

  • Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience
  • Minimum of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries
  • Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):


United States of America - $79,000.00 - $157,000.00


The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

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