Senior Clinical Research Associate

PSI CRO

$80K — $110K *
US-AnywhereRemote in United States
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • College/University degree in Life Sciences or equivalent education/experience
  • Minimum of 5 years independent on-site monitoring in the USA
  • Experience with monitoring Phase I-III clinical trials
  • Prior role as a Senior Monitor in clinical projects
  • Required experience in complex Oncology trials; radiopharmaceuticals and breast cancer experience preferred
  • Preferred experience with GI studies, including IBD, Crohn's, and UC
  • Full working proficiency in English
  • Proficient in MS Office and capable of multitasking in a team environment
  • Strong communication, collaboration, and problem-solving skills
  • Willingness to travel up to 80% of the time
  • Valid driver's license required (if applicable)

Responsibilities

  • Conduct and report onsite monitoring visits
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  • Perform CRF review, source document verification, and resolve queries
  • Manage site communication and activities
  • Supervise study timelines and schedules at the country level
  • Serve as a point of contact for in-house support services and vendors
  • Participate in quality control activities, including compliance monitoring
  • Engage in feasibility research and support regulatory documentation for study submissions

Benefits

  • Advancement opportunities in clinical research
  • Hands-on experience in every aspect of clinical studies
  • Work within a people-first culture at a rapidly growing company
  • Lead full-service projects at the country/regional level
  • Work in a dynamic team environment
Full Job Description
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.

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