What are the responsibilities and job description for the Contract CRA - USA- Minneapolis Minnesota position at Avance Clinical?
We’re Avance Clinical a Contract Research Organization. We offer specialized services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 1980’s. If you already work in this industry, you’ll know that we are experts in our field.
Responsibilities
The Contract Clinical Research Associate (cCRA) performs activities associated with the evaluation, initiation, monitoring and close out of clinical trials to ensure the trial is conducted in accordance with the protocol; company Standard Operating Procedures (SOPs), ICHGCP guidelines and other applicable regulatory requirements.
What we offer
Responsibilities
The Contract Clinical Research Associate (cCRA) performs activities associated with the evaluation, initiation, monitoring and close out of clinical trials to ensure the trial is conducted in accordance with the protocol; company Standard Operating Procedures (SOPs), ICHGCP guidelines and other applicable regulatory requirements.
What we offer
- Stimulating work
- Project diversity
- An intellectual challenge
- An agile & flexible workplace
- Opportunity to progress
- Stability
- Sense of community
- A leadership team that are working together on a common goal
- Flexible work options
- Great tools / tech to do your job
- Bachelor’s level degree in life sciences, pharmacy, nursing or appropriate industry experience.
- At least 12 months experience in the pharmaceutical industry / CRO working in clinical project management
- Formal ICH GCP training (desirable).
- Well developed knowledge of ICH GCP Guidelines and other applicable regulatory requirements.