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Senior Clinical Research Associate

Remote · Morocco Full-time
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, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description:

We are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:

  • Conduct and report SIV, RMV, COV onsite monitoring visits
  • Perform CRF review, source document verification and query resolution
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions
  • Prepare and particiapte on audits and inspections
Qualifications:
  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience
  • Experience in all types of monitoring visits in Phase II and/or III
  • Experience in Oncology is a plus
  • 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
  • Valid driver’s license
Additional Information:

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

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

College/University degree in Life Sciences or equivalent; independent on-site monitoring experience; experience in all monitoring visit types in Phase II/III; full English proficiency; MS Office; valid driver's license; ability to travel; no visa sponsorship.

Key Responsibilities

  • conducting monitoring visits
  • reviewing CRFs
  • managing site communication

Skills & Tools

Microsoft Office

Job Details

  • Category: Research and Development (R&D)
  • Seniority: Mid Level
  • Commitment: Full Time
  • Workplace: Remote — Toronto, Ontario, Canada
  • Salary: CAD 120,000 – 150,000 / year
  • Languages: English

About PSI CRO

A global mid-size clinical research organization founded in 1995, working on the frontline of medical science to bring new medicines to those who need them. — Industry: Research and Development

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