Revance Therapeutics
Revance Therapeutics

62 Revance Clinical Research Associate Jobs Hiring Near You

As a Clinical Research Associate you will work on the frontline of communication with project ... therapeutic indications. You will build and maintain relationships with clinical sites and ...

The Clinical Research Associate will play a key role in site management and study execution ... studies, and therapeutic applications, and to serve as a reliable operational partner in the ...

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...

The Clinical Research Associate will play a key role in site management and study execution ... studies, and therapeutic applications, and to serve as a reliable operational partner in the ...

The Clinical Research Associate will play a key role in site management and study execution ... studies, and therapeutic applications, and to serve as a reliable operational partner in the ...

Therapeutic area experience in neuro- or cardiovascular domain is also required. * Requires ... Senior Clinical Research Associate, Senior CRA, Freelance, Self-employed, Contract, Site Management ...

Are you an experienced Clinical Research Associate seeking to be a pivotal part of launching ... Aria CV won the Transcatheter Cardiovascular Therapeutics 2018 Shark Tank Competition and was named ...

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Clinical Research Associate I

PSI CRO

Remote

Full-time

Posted 9 days ago


Job description

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.
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