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Clinical Research Associate I

PSI CRO
Posted a month ago, valid for 9 days
Salary

$80,000 per year

Contract type

Full Time

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Sonic Summary

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  • The company is a dynamic global organization founded in 1995, focused on medical science and improving lives through new medicines.
  • The Clinical Research Associate will manage communication with project stakeholders, ensuring compliance with clinical research standards and timelines.
  • Candidates must have a college or university degree in Life Sciences and experience as a Study Coordinator or similar role, with a preference for those with Gastroenterology clinical trial experience.
  • The position requires full working proficiency in English, strong PC skills, and the ability to multitask in a dynamic team environment.
  • The compensation for this role is up to USD 80,000 per year, and frequent travel is expected.

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 frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

As a 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
  • 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

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • Experience as a Study Coordinator (or similar role) is required
  • Experience working on Gastroenterology clinical trials preferred 
  • Full working proficiency in English
  • PC skills to be able to work with MS Word, Excel and PowerPoint
  • Ability to plan, multitask and work in a dynamic team environment
  • Communication, collaboration, and problem-solving skills
  • Ability and willingness to travel frequently 
  • Valid driver’s license

Additional Information

Become a full-fledged clinical research professional with the support of a knowledgeable and professional team.  You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.

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

  • Compensation: up to USD 80000 - yearly



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    By applying, a PSI CRO account will be created for you. PSI CRO's Privacy Policy and Terms & Conditions will apply.

    SonicJobs' Terms & Conditions and Privacy Policy also apply.