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Clinical Project Associate Jobs in Gaithersburg, MD

Emmes

Sr. Clinical Research Associate

Rockville, MD · On-site +1

Overview Sr. Clinical Research Associate US remotely and on-site (80% travel) Be Part of One Team ... Under minimal supervision of the project CRA staff oversight lead (i.e. Clinical Study Manager ...

Emmes

Sr. Clinical Research Associate

Rockville, MD · On-site

$80 - $110/hr

Overview Sr. Clinical Research Associate Be Part of One Team, One Purpose. At Emmes Group , we're ... Under minimal supervision of the project CRA staff oversight lead (i.e. Clinical Study Manager ...

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Clinical Project Associate information

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$13

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How much do clinical project associate jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical project associate in Gaithersburg, MD is $34.08, according to ZipRecruiter salary data. Most workers in this role earn between $22.84 and $44.95 per hour, depending on experience, location, and employer.

What is a clinical project associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a clinical project associate?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a clinical project associate?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in Gaithersburg, MD?

The most popular types of Clinical Project jobs in Gaithersburg, MD are:

What are popular job titles related to Clinical Project Associate jobs in Gaithersburg, MD?

For Clinical Project Associate jobs in Gaithersburg, MD, the most frequently searched job titles are:

What job categories do people searching Clinical Project Associate jobs in Gaithersburg, MD look for?

The top searched job categories for Clinical Project Associate jobs in Gaithersburg, MD are:

What cities near Gaithersburg, MD are hiring for Clinical Project Associate jobs?

Cities near Gaithersburg, MD with the most Clinical Project Associate job openings:

Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Gaithersburg, MD as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 19% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $70,882 per year, or $34.1 per hour.

Associate Project Manager or Project Manager

Smithers-Pds-

Gaithersburg, MD • On-site

$88 - $130/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago

Key responsibilities

  • Serve as the client's primary point of contact and oversee the conduct of studies to ensure deliverables are met on-time, within scope, and quality standards.

  • Interpret, analyze, and report data related to validation and sample analysis of biopharmaceutical products.

  • Provide technical advice to scientific staff and ensure compliance with GLP, FDA guidelines, and industry standards.

Job description

Associate Project Manager or Project Manager

Job Category : Operations

Requisition Number : ASSOC002389

  • Posted : August 17, 2026
  • Full-Time
  • Hybrid
Locations

Showing 1 location

Gaithersburg
11 Firstfield Road
Gaithersburg, MD 20878, USA

Gaithersburg
11 Firstfield Road
Gaithersburg, MD 20878, USA

Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development. PDS works with customers to develop new methods, validate existing methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials currently in different phases of the FDA regulated drug approval process. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories.

Smithers PDS is seeking an Associate Project Manager or Project Manager who will be responsible for being the client's primary point of contact and for the overall conduct of the study. The role ensures deliverables are met on-time, within scope, and within established quality standards.

This position is classified as exempt and paid on a salary basis. Exempt employees typically work 40 hours or more to adequately perform their responsibilities. Extended work hours may be necessary to support the business in meeting client deliverable commitments. Position is generally eligible for a hybrid work schedule with at least three days on-site once all training requirements have been adequately met and proficient performance is consistently demonstrated.

The annualized salary range for an Associate Project Manager or Project Manager position is $87,500 -112,500 or $105,000 - $130,000, respectively. Experience and qualifications will determine salary and job level. Smithers PDS offers a comprehensive health insurance package including a choice of 3 medical plans, dental insurance, vision insurance, 401K retirement plan and PTO.

  • Responsible for client interaction and the conduct of studies.
  • Serve as Principal Investigator for GLP studies
  • Responsible for data interpretation, analysis, and reporting of results for validation and sample analysis of biopharmaceutical products.
  • Provide technical advice to scientific staff.
  • Experience and knowledge of Ligand-binding assays (ELISA / MSD) applicable to Pharmacokinetic, Biomarker and Immunogenicity studies is required.
  • Must understand contract immunoanalytical business objectives and is expected to be familiar with regulatory, and GLP requirements, FDA guidelines and industry standards for bioanalytical method validation.
  • Knowledge of Watson LIMS a plus.
  • Additional responsibilities include forecast of revenue, preparing and revising SOPs.

Minimum Qualifications:

  • B.S. / B.A. degree in Biology or related field and a minimum of 5 years of relevant experience in the CRO industry; or, advanced degree in Biology or related field and at least 2 years of relevant experience in the CRO industry.
  • Knowledge of GLP regulations and regulatory guidelines.
  • Excellent communication skills, both oral and written.
  • Strong leadership and excellent organizational skills.
  • Proficient in the use of basic computer applications such as MS Word and Excel.

Additional Position Requirements:

  • Ability to multi-task and produce quality analysis while working under the pressure of strict deadlines.
  • Proficient in time management and resource planning.
  • Ability to initiate and implement self-development efforts.
  • Ability to effectively interact with clients and regulatory personnel.
  • Ability to make decisions and complete assignments with minimal supervision.
  • Ability to self-direct work priorities.

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