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Clinical Study Associate Jobs in Maryland (NOW HIRING)

Emmes Group

Study Start-Up Associate II

Rockville, MD · On-site

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

BD Mexico

$76 - $121/hr

The Clinical Research Associate (CRA) is responsible for the management and monitoring of assigned ... This role ensures studies are conducted in compliance with Good Clinical Practice (GCP), applicable ...

New

Emmes

Study Start-Up Associate II

Rockville, MD · On-site +1

$34.25 - $46.75/hr

Overview Study Start-Up Associate II US Remote Emmes Group: Building a better future for us all ... Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

MSD

Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor ... Associate's degree, certificate or equivalent in a scientific / healthcare discipline together with ...

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Clinical Study Associate information

See Maryland salary details

$12

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$53

How much do clinical study associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical study associate in Maryland is $30.61, according to ZipRecruiter salary data. Most workers in this role earn between $20.53 and $40.38 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.

What are the key skills and qualifications needed to thrive as a clinical study associate, and why are they important?

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What is the difference between Clinical Study Associate vs Clinical Research Coordinator?

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

The most popular types of Clinical Study jobs in Maryland are:

Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Maryland as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $63,671 per year, or $30.6 per hour.

Clinical Applications Programmer II

Pharmaron

Baltimore, MD • On-site

$60K - $70K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago

Job description

Position: Clinical Applications Programmer II
Salary Range: $60,000-70,000
Location: Baltimore, MD
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
What You'll Do
We are seeking a Clinical Systems Programmer II to support the configuration, programming, validation, and ongoing management of electronic systems used to collect, process, and analyze clinical study data. This role will work closely with Clinical Data Management, Clinical Operations, Laboratory, IT, Regulatory, project teams, and study sponsors to ensure clinical systems are designed, tested, documented, and maintained in accordance with study requirements and industry standards.
The ideal candidate combines clinical research knowledge, EDC/eSource programming experience, clinical database design, and familiarity with CDISC standards and 21 CFR Part 11 requirements. This is a hands-on role for someone who enjoys solving complex system and data challenges while ensuring high-quality, compliant clinical data collection.
Key Responsibilities
  • Configure eSource, EDC, Laboratory Information Systems, and other clinical systems based on study protocols, laboratory manuals, pharmacy manuals, and related study documentation.
  • Create and maintain CDISC/CDASH-compliant eCRFs, study workflows, dynamic forms, and conditional logic.
  • Program screening, inpatient, and follow-up workflows in accordance with study protocols and source templates.
  • Develop and maintain edit checks and data validation rules using logic operators to authenticate data entered into electronic forms.
  • Utilize basic JavaScript or similar programming languages to create and modify methods, edit checks, and study-specific functionality.
  • Develop User Acceptance Testing (UAT) documentation and support Clinical Information Specialists in completing UAT activities.
  • Troubleshoot system issues, investigate defects, and implement appropriate solutions.
  • Participate in meetings with Project Managers, clinical and laboratory leaders, and study sponsors to ensure systems capture, process, and report required study data.
  • Collaborate with Clinical Systems leadership, IT, and Regulatory teams on system upgrades, implementation timelines, and validation activities.
  • Assist with the development of templates, SOPs, training materials, and standardized practices to improve efficiency and minimize study-specific build time.
  • Meet established programming, testing, and study implementation deadlines.
  • Maintain comprehensive documentation to support audit readiness and regulatory compliance.
  • Provide system training and ongoing technical support to subject matter experts and end users.
  • Serve as the primary systems point of contact for assigned clinical studies.
  • Work independently while collaborating effectively with the Data Management team and cross-functional stakeholders.
  • Support compliance with Good Clinical Practice (GCP), CDISC standards, 21 CFR Part 11, and applicable clinical research requirements.

What We're Looking For
Required Qualifications
  • High school diploma plus 4 years of relevant experience in at least two of the following areas; OR
  • Associate degree/equivalency (60+ college credit hours) plus 2 years of relevant experience in at least two of the following areas; OR
  • Bachelor's degree/equivalency (120+ college credit hours) plus 1 year of relevant experience in at least two of the following areas:
    • Clinical research, life sciences, public health, or related field
    • eSource or EDC study design and configuration
    • Application support
    • System validation and User Acceptance Testing
    • CDISC terminology and standards
    • JavaScript or other programming languages

Knowledge & Skills
  • Understanding of Good Clinical Practice (GCP) and clinical research processes.
  • Working knowledge of CDISC standards, including CDASH and SDTM concepts.
  • Experience designing data collection solutions that support standardized clinical trial data capture and reporting.
  • Basic proficiency with JavaScript or a similar programming language.
  • Strong analytical and critical-thinking skills with the ability to troubleshoot complex system and data issues.
  • Strong quality-control and testing skills.
  • Ability to analyze system requirements and evaluate how system changes may impact clinical study operations and data.
  • Excellent communication and active-listening skills.
  • Ability to manage multiple priorities and meet programming and testing deadlines.
  • Ability to work independently and collaboratively across functional teams.
  • Strong attention to detail and commitment to data quality and regulatory compliance.

Preferred Qualifications
  • Master's degree in Computer Science, Health Informatics, Clinical Research, Data Science, or a related field.
  • Industry certifications in clinical research, data management, EDC systems, programming, or related disciplines.
  • Experience with Active Directory administration.
  • Network troubleshooting experience.
  • Application support experience.
  • Laboratory, pharmacy, or clinical application experience.
  • Web design, programming, and/or web administration experience.
  • Experience with MySQL, PostgreSQL, Microsoft SQL, Oracle, and/or Microsoft Access.
  • Laboratory, pharmacy, or clinical management experience.

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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