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Remotavia
PSI CRO

Senior Clinical Research Associate

Remote in set countriesUnited States onlyFull-time

Posted 27 days agoConfirmed open 2h ago

Who can apply

United States only

Salary

Not disclosed

Level

Entry level

Full-time

Timezone

Not stated

About the role

Job Description

As a Senior Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

You will:

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup (if applicable)
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Supervise study activities, timelines, and schedules on the country level
  • Be a point of contact for in-house support services and vendors
  • Be involved in quality control, such as compliance monitoring and reports review
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in the USA (5 years minimum)
  • Experience in all types of monitoring visits in Phase I-III
  • Participation in clinical projects as a Senior Monitor
  • Experience monitoring complex Oncology trials required; experience with radiopharmaceuticals and/or breast cancer preferred
  • Experience monitoring GI studies (IBD, Chron's, UC) is preferred. 
  • Full working proficiency in English
  • Proficiency in MS Office applications
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability to travel up to 80%
  • Valid driver’s license (if applicable)

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

Additional Information

Advance your career in clinical research and lead challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first! You will get hands-on involvement in every aspect of the study.

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

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.  A dynamic, global company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals.  We work on the front-line of medical science, changing lives, and bringing new medicines to those who need them.

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

Skills mentioned

Interested in this role?

You apply directly with PSI CRO. Remotavia never charges candidates.

Apply on PSI CRO's site

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Listing details & historyShow
Employer posted
28 Sept 2026
Last confirmed open
2h ago
Source
Employer careers site
Degree
Degree preferred
“You will: Conduct and report all types of onsite monitoring visits Be involved in study startup (if applicable) Perform CRF review, source document verification and query resolution Be responsible for site communication and management Supervise study activities, timelines, and schedules on the country level Be a point of contact for in-house suppor”
Visa
Not stated
Timezone
Not stated
Languages
English
Location evidence
“Remote (Remote, US, United States)”

Details are read from the listing text. They are not a guarantee of work authorization; confirm with the employer.

History

  • 14 Oct · Added to Remotavia
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