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Clinical Data Management Associate Jobs in Maryland

CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...

CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...

CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...

Clinical Database Developer

Fort Detrick, MD · On-site

$125K - $150K/yr

The individual ensures clinical databases meet FDA regulatory requirements, ICH guidelines, Good Clinical Data Management Practices (GCDMP), and CDISC standards, while supporting data collection ...

Data management support includes performing clinical data management activities or providing clinical data management oversight, support responsibilities. Provide biostatistical support and ...

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Clinical Data Management Associate information

See Maryland salary details

$13

$37

$84

How much do clinical data management associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for clinical data management associate in Maryland is $37.80, according to ZipRecruiter salary data. Most workers in this role earn between $28.46 and $37.79 per hour, depending on experience, location, and employer.

What is the difference between Clinical Data Management Associate vs Clinical Data Coordinator?

AspectClinical Data Management AssociateClinical Data Coordinator
ResponsibilitiesData entry, validation, database management, ensuring data qualityOversees data collection, manages databases, coordinates data flow between teams
Required SkillsAttention to detail, knowledge of clinical data systems, basic understanding of regulationsStrong organizational skills, data management experience, communication skills
Work EnvironmentClinical research labs, CROs, pharmaceutical companiesClinical trial sites, research organizations, CROs
Common UsageEntry to mid-level data roles in clinical trialsData oversight and coordination roles in clinical studies

The Clinical Data Management Associate focuses on data entry, validation, and database management, ensuring data accuracy. The Clinical Data Coordinator oversees data collection and flow, coordinating between teams. Both roles require similar skills and work environments but differ in scope and responsibilities.

What does a Clinical Data Management Associate do?

A Clinical Data Management Associate is responsible for collecting, cleaning, and maintaining clinical trial data to ensure accuracy and compliance. They use specialized software to manage data, perform quality checks, and support the integrity of clinical research studies. Strong attention to detail and knowledge of regulatory standards are essential in this role.

What are the most commonly searched types of Clinical Data Management jobs in Maryland?

The most popular types of Clinical Data Management jobs in Maryland are:

What cities in Maryland are hiring for Clinical Data Management Associate jobs?

Cities in Maryland with the most Clinical Data Management Associate job openings:

Senior Manager, Clinical Data Management

Gaithersburg, MD

$130K - $209K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 19 days ago


Job description

Cambridge, US; Gaithersburg, US; New Jersey, US   |   full time   |   Job ID: 11678 

About the role:

At BioNTech, we are more than a biotechnology company - we are a community of innovators dedicated to revolutionizing medicine. As a Senior Manager Clinical Data Management, you will play a pivotal role in ensuring the integrity and quality of clinical data that drives groundbreaking research and development. You will be at the forefront of managing data processes that contribute to advancing our diversified portfolio of product candidates. Join us in shaping the future of medicine within an environment that values collaboration, innovation, and diversity.

Your contribution:

  • Serve as the primary point of contact for partners and sub-contractors on data management deliverables and activities
  • Provide technical expertise while collaborating with CRO data managers for end-to-end clinical data management activities
  • Supervise clinical data management tasks, negotiating timelines, processes, and addressing quality issues directly with CROs
  • Organize and oversee clinical data management activities aligned with BioNTech's strategy and standards
  • Participate in protocol development, creating and validating essential documents such as CRFs and validation plans
  • Ensure compliance with Good Clinical Practices (GCPs) and regulatory guidelines while supporting medical review processes

A good match:

  • University degree in natural/life sciences or equivalent experience in Clinical Data Management within CRO/biotechnology/pharmaceutical settings with 7-10 years of experience in Clinical Data Management,
  • Profound knowledge of international guidelines (ICH-GCP) for clinical research projects
  • Experience with Clinical Database Systems like Medidata or OCRDC along with proficiency in MS Office tools (Word, Excel, PowerPoint)
  • Excellent organizational skills, attention to detail, and ability to work independently while being proactive
  • Strong communication skills paired with a team-oriented mindset

At BioNTech, your work has the potential to impact lives globally. Apply today to become part of our mission-driven team!

Your benefits and remuneration:

Expected Pay Range: $130,800/year to $209,400/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.

BioNTech US is committed to employee wellbeing and offers best-in-class benefits & HR programs to support an inclusive & diverse workforce. Salaried/Position-Targeted Hourly Employees working 30+ hours per week are eligible for our comprehensive benefits package. Benefits include but are not limited to:

  • Medical, Dental and Vision Insurance
  • Life, AD&D, Critical Illness Insurance
  • Pre-tax HSA & FSA, DCRA Spending Accounts
  • Employee Assistance & Concierge Program (EAP) available 24/7
  • Parental and Childbirth Leave & Family Planning Assistance
  • Sitterstream: Virtual Tutoring & Childcare Membership
  • Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.
  • 401(K) Plan with Company Match
  • Tuition Reimbursement & Student Loan Assistance Programs
  • Wellbeing Incentive Platforms & Incentives
  • Professional Development Programs
  • Commuting Allowance and subsidized parking
  • Discounted Home, Auto & Pet Insurance

...and more! More details to be shared.
 

Home to dozens of research institutions, biopharmaceutical companies, life science incubators, venture capital firms, and over 30 million square feet of laboratory space, Cambridge, Massachusetts has earned a reputation as the #1 life science cluster in the world. As part of the Greater Boston area, the city is often referred to as the "biotech supercluster" due to its high concentration of life sciences firms. This unique ecosystem is the result of a model partnership between academia and industry, fostering collaboration and innovation and driving the development of new therapies, medical devices, and diagnostics. As Cambridge's thriving life sciences industry continues to evolve, the city remains a beacon of knowledge, innovation, and collaboration, poised to shape the future of science and technology.

Apply now - We look forward to your application!

Apply for our Cambridge, US; Gaithersburg, US; New Jersey, US location and simply send us your documents using our online form.

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.