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Data Review Scientist Jobs in Silver Spring, MD (NOW HIRING)

Scientific Data Analyst

Vienna, VA · On-site

$85K - $115K/yr

Scientific Data Analyst Clearance Required: Public Trust - Federal Client requires US Citizenship ... Review data error logs to ensure that requested data modifications are done according to the ...

Scientific Data Analyst

Vienna, VA · On-site +1

$85K - $115K/yr

Scientific Data Analyst Clearance Required: Public Trust - Federal Client requires US Citizenship ... Review data error logs to ensure that requested data modifications are done according to the ...

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Data Review Scientist information

See Silver Spring, MD salary details

$38.6K

$126.5K

$202.5K

How much do data review scientist jobs pay per year?

As of Jul 31, 2026, the average yearly pay for data review scientist in Silver Spring, MD is $126,496.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,500.00 and $140,200.00 per year, depending on experience, location, and employer.

What is the difference between Data Review Scientist vs Data Analyst?

AspectData Review ScientistData Analyst
Required CredentialsBachelor's degree in data science, statistics, or related field; familiarity with data review toolsBachelor's degree in data analysis, statistics, or related field; proficiency in data visualization and analysis software
Work EnvironmentHealthcare, clinical trials, or research settings focusing on data quality and complianceBusiness, marketing, finance, or operations across various industries analyzing data trends
Employer & Industry UsagePharmaceutical companies, research institutions, healthcare organizationsCorporations, marketing agencies, financial firms, and tech companies

While both roles involve working with data, Data Review Scientists primarily focus on ensuring data quality and compliance in research or clinical settings, whereas Data Analysts interpret data to inform business decisions across diverse industries.

What are some common challenges faced by Data Review Scientists when ensuring data integrity in research projects?

Data Review Scientists often encounter challenges such as identifying inconsistencies in large datasets, resolving discrepancies between source documents and digital records, and ensuring strict adherence to regulatory standards like GLP or GCP. They must also coordinate with cross-functional teams, including laboratory staff and data managers, to clarify data queries and implement corrective actions promptly. Staying updated with evolving data management technologies and regulatory requirements is crucial for success and helps maintain the highest levels of data integrity throughout research projects.

What are the key skills and qualifications needed to thrive as a Data Review Scientist, and why are they important?

To thrive as a Data Review Scientist, you need a solid background in life sciences or related fields, strong analytical skills, and experience with data validation and interpretation. Familiarity with data management systems such as LIMS, proficiency in statistical analysis tools like SAS or R, and knowledge of regulatory guidelines (e.g., GxP, FDA) are typically required. Attention to detail, critical thinking, and effective communication help ensure accuracy and clarity when reviewing complex datasets and collaborating with cross-functional teams. These skills are crucial for maintaining data integrity and supporting regulatory compliance in scientific research and clinical trials.

What does a Data Review Scientist do?

A Data Review Scientist is responsible for reviewing, validating, and interpreting scientific data to ensure its accuracy, integrity, and compliance with regulatory standards. They often work in pharmaceutical, clinical, or research settings, analyzing experimental or clinical trial data for errors, inconsistencies, and completeness. Their work helps ensure that scientific findings are reliable and can be used to support research conclusions or regulatory submissions.
What are popular job titles related to Data Review Scientist jobs in Silver Spring, MD? For Data Review Scientist jobs in Silver Spring, MD, the most frequently searched job titles are:
What cities near Silver Spring, MD are hiring for Data Review Scientist jobs? Cities near Silver Spring, MD with the most Data Review Scientist job openings:
Infographic showing various Data Review Scientist job openings in Silver Spring, MD as of July 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, and 3% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $126,496 per year, or $60.8 per hour.

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This job post has expired today. Applications are no longer accepted.


Syneos Health rating

8.1

Company rating: 8.1 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

37th of 86 rated pharmaceutical


Job description

Clinical Scientist - Respiratory

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to our Total Self culture - where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong.

Job Responsibilities

* Works with Medical Director to develop medical plans (Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan). Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary medical/scientific input to prepare the respective medical plans.

* Performs regular and ad-hoc medical review of data listings and data visualization as needed; analyzes the data to identify risks and data patterns/trends and supports documentation of medical reviews.

* Authors medical data queries and reviews query responses, approves query closure in association with Medical Director.

* May assist Medical Director in patient profiles review, scientific review of other study level data, protocol deviation review, creation of Medical Review Summary report as needed.

* Partners with Medical Directors for medical data review meetings and safety review meetings including slide preparation as needed.

* Manages project scope of work, objectives, and quality of deliverables to ensure the project specific milestones and timelines are met. Serves as primary interface between internal team, customers, and vendors in the areas of medical data review and eligibility review.

* Collaborates with study team members including Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management (set-up and/or lead meetings as appropriate) to identify risks related to data integrity and subject safety. Escalates ongoing and newly developed study concerns such as at-risk project deliverables and out of-scope tasks to the project leads in a timely manner.

* Attends at Trusted Process meetings and may participate in internal and external audits.

* Acquires basic understanding and knowledge of ongoing protocol designs and disease related terminology and pathology.

* Adheres to all data privacy guidelines, International Committee on Harmonization (ICH), and Good Clinical Practices (GCPs), all enterprise policies, standard operating procedures, work instructions, and project plans. Adheres to customer policies and standard operating procedures, as required in project plans.

We are always excited to connect with great talent. This posting is intended for a [possible] upcoming opportunity rather than a live role. By expressing your interest, you'll be added to our talent pipeline and considered should this role become available.

At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.

Salary Range:

The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role.

Get to know Syneos Health


Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you'll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information


Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.


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