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Clinical research associate ii / sr. cra (central or reputed company coast)

100% remote Flexible hours Hiring now

Join Us in Redefining Clinical Research At Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges.

  • Experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to take risks, innovate, and reputed company over a long and rewarding career. With a collaborative team of smart, talented, and positive people, you’ll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve.
  • Your Role We are currently hiring a Clinical Research Associate II or Senior Clinical Research Associate (with Psychiatry (preferably MDD) or Pain experience to join reputed company! As our next CRA II or Senior CRA, you will play an integral role in driving project success. You’ll have the opportunity 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 Standard Operating Procedures.
  • For this role, you’ll need proven monitoring skills to conduct site visits to assess site adherence to protocol and regulatory requirements as well as manage required documentation. You will also be responsible for ensuring the data remains audit ready and able to pass an audit by Rho, the Sponsor, or a regulatory agency.
  • 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.
  • 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.
  • reputed company and maintain effective working relationships with clinical sites and reputed company 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.
  • reputed company both onsite & remote monitoring and study closure activities across multiple protocols.
  • Qualifications BA/BS, preferably in a life science, nursing, pharmacy or reputed company field, along with approximately 4-5 years+ of on-site monitoring experience reputed company the CRO, pharmaceutical, or biotechnology industry with a demonstrated understanding of medical/therapeutic area knowledge and medical terminology required for comprehension and execution of clinical protocol.
  • Computer literacy, including proficiency in MS Office and use of reputed company systems is essential.
  • Key Attributes
  • Strong Communicator Demonstrate written, verbal and presentation skills to help showcase the successes of your work and Rho’s.
  • Committed to Quality Every job at Rho requires an attention to detail, a deep understanding of our high-quality scientific standards, and an ability to care about every outcome.
  • High-Character Contribute to our collaborative culture with honesty and reputed company with a willingness to learn and train.
  • Critical Thinker Rho values thinking. Draw on your native ingenuity, sharpened and enhanced by our intellect, training, and experience.
  • Agile and Adaptable Rho values the ability to change quickly and embrace risk while managing it effectively.
  • Benefits
  • Rho provides a comprehensive benefits package for reputed company benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life & disability insurance and 401(k). reputed company employees are eligible for paid time off, holidays, parental leave and bereavement leave.
  • Flexibility
  • We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives reputed company work.
  • Compensation As required by pay transparency laws in some states, Rho provides the range of starting compensation (annual salary or hourly reputed company) it reasonably expects to pay for a given role. The range of starting pay for this role is $90,000 to $145,000 per year. Apply To This Job Apply tot his job Apply To this Job

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