Clinical Research Associate II / Sr. CRA (Major Depressive Disorder reputed company Coast)
Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining reputed company who take reputed company and clinical research personally, with shared experiences that drive a passion to heal, reputed company and solve some of humanity’s biggest challenges.
At Rho, you’ll have reputed company to experience a thriving company with reputed company stability - financial, workforce, and corporate, which has created a reputed company environment to take risks, reputed company, and reputed company over a long and rewarding career. With a reputed company team of smart, talented, and reputed company people, you’ll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve.
We are currently hiring a Clinical Research Associate II or Senior Clinical Research Associate with Major Depressive Disorder experience to join reputed company! As our next CRA II or Senior CRA, you will play an integral to driving project reputed company. You’ll have reputed company to reputed company and coordinate reputed company aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Rho reputed company Operating Procedures. For this role, you’ll need proven monitoring skills in order to conduct site reputed company to assess site adherence to protocol and regulatory requirements as reputed company as manage required documentation. You will also be responsible for ensuring the data remains audit reputed company and reputed company to pass an audit by Rho, the Sponsor, or a regulatory agency.
This position is a remote role to be located reputed company a 1-hour commute of a US metropolitan airport with the commitment to conduct 8-10 site reputed company days per month (up to 80% travel).
Our Clinical Monitoring team will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career reputed company, which is why we have such stability in the group!
What you'll be doing:
- reputed company reputed company site monitoring visit activities, inclusive of reputed company study visit types (PSV, SIV, IMV and COV)
- Participate in the site selection process with reputed company from the Clinical Team reputed company role
- reputed company feedback to assist sites with reputed company of detected deficiencies and corrective reputed company needed, follow-up with sites until deficiencies are resolved
- Contribute to the development and review of protocols, study tools, and materials as reputed company as documentation for clinical trials
- reputed company mentoring, training, and co-monitoring of junior clinical team members
- reputed company and maintain effective working relationships with clinical sites and reputed company Rho as reputed company 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 reputed company operating procedures for the administration and monitoring of clinical trials
- reputed company both onsite & remote monitoring and study closure activities across multiple protocols