What are the responsibilities and job description for the Clinical Research Associate - Phoenix, Arizona position at Celerion?
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Celerion, a leader in clinical research, is seeking a full-time Clinical Research Associate (CRA) to perform monitoring and site management activities for clinical trials, clinical investigations and other interventional or non-interventional studies.
This is a Hybrid position - We are looking for someone that currently lives in the Phoenix, Arizona area - and that is able to go to the Tempe site on a regular basis.
\n- Clinical monitoring and site management for national and international clinical studies of phases I-IV
- Regulatory activities with authorities, ethics committees and investigators
- Project management support and in-house activities for clinical research projects
- Sponsor communication and contact
- BA/BS degree in biomedical-related field, life sciences or equivalent field
- Two years working experience in clinical research, as a CRA, Study Nurse or related profession preferred
- One year experience in on-site monitoring preferred
- Excellent oral and written communication skills in English
- High level of organization, multi-tasking, judgement, and keeping to timelines
- Profound knowledge of ICH-GCP and other relevant regulatory requirements
- Flexible and willing to possibly travel to other sites
- Anticipate & prevent problems. Able to create backup plans
Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
