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Remote Clinical Trials Data Analyst Jobs (NOW HIRING)

Review patient clinical records and use relevant data to determine clinical trial matches ... Experience in critically evaluating clinical trials. * Basic knowledge of generative AI. CHI: $46 ...

Clinical Trials Manager (CTM) Location: Remote Schedule: Full-Time | Eastern Time Zone Hours Pay ... Collaborate with Project Managers, clinical teams, data management, and other departments to meet ...

... data and analysis infrastructure platforms and other technical solutions to support the data flow from data collection to data submission. Using expertise in R programming and clinical trials to ...

Clinical Data Manager

Austin, TX · Remote

$125K - $175K/yr

... active clinical trials. This individual will play a critical role in ensuring high-quality ... Remote (U.S.) Responsibilities: * Lead day-to-day data management activities for assigned clinical ...

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... documents (protocols, statistical analysis plans, CRFs, study reports) and processes.

Design, implement, and manage all data management activities for assigned clinical trials ... Excellent problem-solving and analytical skills. * Knowledge of database structures and available ...

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How much do remote clinical trials data analyst jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for remote clinical trials data analyst in the United States is $36.36, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $42.07 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Trials Data Analyst vs Remote Clinical Research Coordinator?

AspectRemote Clinical Trials Data AnalystRemote Clinical Research Coordinator
Primary RoleAnalyzes clinical trial data, manages databases, generates reportsCoordinates trial activities, manages site operations, ensures protocol compliance
Required SkillsData analysis, statistical software, attention to detailCommunication, organization, regulatory knowledge
Work EnvironmentRemote, primarily computer-basedRemote or onsite, site management
Common CertificationsCertified Clinical Data Manager (CCDM), related data certificationsCertified Clinical Research Professional (CCRP), site management certifications

The Remote Clinical Trials Data Analyst focuses on analyzing and managing clinical data remotely, while the Remote Clinical Research Coordinator handles trial coordination and site management. Both roles require understanding of clinical research but differ in daily tasks and skill sets.

More about Remote Clinical Trials Data Analyst jobs

What cities are hiring for Remote Clinical Trials Data Analyst jobs?

Cities with the most Remote Clinical Trials Data Analyst job openings:

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

The most popular types of Clinical Trials Data Analyst jobs are:

What states have the most Remote Clinical Trials Data Analyst jobs?

States with the most job openings for Remote Clinical Trials Data Analyst jobs include:

Infographic showing various Remote Clinical Trials Data Analyst 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 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $75,625 per year, or $36.4 per hour.

Senior Clinical Data Manager

Remote

Worldwide Clinical Trials
Scientific Research and Development Services • 10K+ employees

Full-time

Re-posted 2 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.