Senior Clinical Research Associate

PSI CRO

• $95K — $115K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • College/University degree in Life Sciences or equivalent experience
  • Minimum of 5 years independent on-site monitoring experience in the USA
  • Experience conducting all types of monitoring visits in Phase I-III studies
  • Proven track record as a Senior Monitor on clinical projects
  • Required experience with complex Oncology trials; radiopharmaceutical and breast cancer experience preferred
  • Preferred GI study monitoring experience (IBD, Crohn's, UC)
  • Full working proficiency in English; MS Office proficiency required

Responsibilities

  • Conduct and report various onsite monitoring visits
  • Participate in study startup activities
  • Perform CRF reviews, verify source documents and resolve queries
  • Manage and communicate with study sites
  • Supervise country-level study activities, timelines, and schedules
  • Act as point of contact for in-house support services and vendors
  • Engage in quality control and compliance monitoring
  • Support regulatory team with study submission documents

Benefits

  • Opportunity to advance in clinical research
  • Involvement in full-service projects at a regional level
  • Growth with a people-first company
  • Dynamic work environment with hands-on study involvement
  • Ability to lead and supervise significant clinical projects.
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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