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Clinical Operations Associate Jobs in Philadelphia, PA

The practice will determine, based on operational need, how much time will be spent in each ... Clinical Services Associates have an opportunity to join our organization and make a difference in ...

The practice will determine, based on operational need, how much time will be spent in each ... Clinical Services Associates have an opportunity to join our organization and make a difference in ...

The practice will determine, based on operational needs, how much time will be spent in each ... Clinical Services Associates have an opportunity to join our organization and make a difference in ...

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Clinical Operations Associate information

See Philadelphia, PA salary details

$10

$25

$51

How much do clinical operations associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical operations associate in Philadelphia, PA is $25.08, according to ZipRecruiter salary data. Most workers in this role earn between $17.02 and $28.94 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the key skills and qualifications needed to thrive in the clinical operations associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the typical responsibilities and team dynamics for a clinical operations associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What are the most commonly searched types of Clinical Operations jobs in Philadelphia, PA?

The most popular types of Clinical Operations jobs in Philadelphia, PA are:

What are popular job titles related to Clinical Operations Associate jobs in Philadelphia, PA?

For Clinical Operations Associate jobs in Philadelphia, PA, the most frequently searched job titles are:

What job categories do people searching Clinical Operations Associate jobs in Philadelphia, PA look for?

The top searched job categories for Clinical Operations Associate jobs in Philadelphia, PA are:

What cities near Philadelphia, PA are hiring for Clinical Operations Associate jobs?

Cities near Philadelphia, PA with the most Clinical Operations Associate job openings:

Infographic showing various Clinical Operations Associate job openings in Philadelphia, PA as of August 2026, with employment types broken down into 88% Full Time, and 12% Part Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $52,171 per year, or $25.1 per hour.

Project Coordination Associate

PSI CRO

King Of Prussia, PA โ€ข On-site

Full-time

Re-posted 5 days ago


Job description

Company Description

We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do.ย  A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals.ย  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

The Project Coordination Associate supervises and coordinates trial administrative support, management of trial records, site management, and communication with the investigator sites, the sponsor, trial vendors, and members of the project team. This function operates at a regional or global trial level.

Responsibilities Include:

  • Ensures planning, implementation, and management of trials in compliance with industry regulations, ICH-GCP, essential trial records and applicable controlled documents (e.g., PSI QSDs or Sponsor QMS documents)
  • Ensures consistency of Clinical Operations processes in the assigned trials across the trial regions
  • Organizes the exchange of trial-specific information and records with sites, sponsors, and vendors
  • Participates in and follows up on regulatory and ethics committee submissions and notifications
  • Tracks the financial and contractual tasks within the project team
  • Supervises the preparation for and follow-up on site audits and inspections
  • Organizes, participates in and prepares reports of project meetings
  • Organizes, attends, and follows up on Investigator Meetings
  • Conducts on-the-job coaching of Site Management Associates and Clinical Operations Administrative Support staff
  • Coordinates and monitors compliance of trial-specific trainings of the project team
  • Supervises site and trial handovers between Site Management Associates Project Coordination Associate
  • Maintains and overseesย the regular TMF quality checks for completeness and accuracy
  • Prepares for and follows up on system audits and inspections
  • Supervises the preparation, distribution, and update of ISFs and ISF checklists
  • Supervises the translation process for trial records on a regional and global level
  • Maintains and reviews trial-specific and corporate tracking management systems
  • Supervises the timely update of trial-specific and corporate tracking management systems done by the project team
  • Coordinates clinical supplies order, receipt, inventory, storage, distribution, return/recall, and reconciliation, and maintains accurate records of thereof
  • Drafts and tracks project plans
  • Initiates and supervises the trial-specific IP-REDs review process
  • Supervises performance of Site Management Associates
  • Performs other assigned trial coordination tasks as delegated by the Project Manage
Qualifications
  • College or university degree in Life Sciences or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities is considered sufficient.
  • Minimumย four years of CRO and/or relevant clinical research experience required
  • Must beย in a commutable distance to the office inย King of Prussia, PA
  • Strong communication and presentation skills
  • Attention to detailย and organizational skills are critical
  • Ability to work in a team setting as well as independently as needed
  • Proficient in using Microsoft Office tools
Additional Information

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then this is the right choice for you.

For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future