Senior Clinical Research Associate (West Coast or Central)
R
Rho IncCRO, Pharmaceutical, Biotechnology
United StatesFull-TimeSenior
Salary90000 - 145000 USD per year
Apply NowOpens the employer's application page
Job Details
- Experience
- 4-5 years+
- Required Skills
- MS Office
Requirements
- BA/BS, preferably in a life science, nursing, pharmacy or related field
- 4-5 years+ of on-site monitoring experience within the CRO, pharmaceutical, or biotechnology industry
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- Computer literacy, including proficiency in MS Office and use of EDC systems
- Strong written, verbal and presentation skills
- Strong organization skills
- Honesty and integrity with a willingness to learn and train
- Native ingenuity, sharpened and enhanced by intellect, training, and experience
- Ability to change quickly and adapt
- Proven monitoring skills
- Experience with Psychiatry (preferably MDD)
Responsibilities
- Perform all site monitoring visit activities, inclusive of all study visit types (PSV, SIV, IMV and COV)
- Participate in the site selection process with oversight from the Clinical Team Lead role
- Provide feedback to assist sites with resolution of detected deficiencies and corrective action needed, follow-up with sites until deficiencies are resolved
- Contribute to the development and review of protocols, study tools, and materials as well as documentation for clinical trials
- Provide mentoring, training, and co-monitoring of junior clinical team members
- Develop and maintain effective working relationships with clinical sites and within Rho as well as ensure communication of project goals and critical requirements
- Attend and present at meetings and conferences, including Investigator Meetings
- Participate in the RFP process, including business development meetings
- Participate in the Clinical Operations community at Rho by contributing to internal initiatives and standard operating procedures for the administration and monitoring of clinical trials
- Perform both onsite & remote monitoring and study closure activities across multiple protocols
View Full Description & ApplyYou'll be redirected to the employer's site