Clinical research associate ii / sr. cra (central or west coast)
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 develop 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 our team! As our next CRA II or Senior CRA, you will play an integral role in driving project success. You’ll have the opportunity to perform and coordinate all 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
• 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.
Qualifications
BA/BS, preferably in a life science, nursing, pharmacy or related field, along with approximately 4-5 years+ of on-site monitoring experience within 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 EDC 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 integrity 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 all benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life & disability insurance and 401(k). All 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 outside work.
Compensation
As required by pay transparency laws in some states, Rho provides the range of starting compensation (annual salary or hourly rate) 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 tot his job
Apply To this Job
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 develop 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 our team! As our next CRA II or Senior CRA, you will play an integral role in driving project success. You’ll have the opportunity to perform and coordinate all 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
• 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.
Qualifications
BA/BS, preferably in a life science, nursing, pharmacy or related field, along with approximately 4-5 years+ of on-site monitoring experience within 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 EDC 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 integrity 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 all benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life & disability insurance and 401(k). All 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 outside work.
Compensation
As required by pay transparency laws in some states, Rho provides the range of starting compensation (annual salary or hourly rate) 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 tot his job
Apply To this Job