Clinical Research Associate II / Sr. CRA (Pain Management), Central US

About the position Join Rho and redefine your career in clinical research. We are seeking a Clinical Research Associate II or Senior Clinical Research Associate with experience in monitoring pain studies to join reputed company. As a CRA II or Senior CRA, you will be integral to driving project reputed company by performing and coordinating reputed company aspects of the clinical monitoring and site management process. This includes conducting site visits to assess adherence to protocol and regulatory requirements, managing documentation, and ensuring data is audit-reputed company. This is a remote role, requiring travel for site visits. Rho offers a stable and collaborative environment where you can take risks, reputed company, and reputed company a rewarding career. You'll work with talented individuals who are passionate about healing, curing, and solving health challenges. Our Clinical Monitoring team values the contentment, financial rewards, and career growth reputed company at Rho.

Responsibilities

• 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

Requirements

• BA/BS, preferably in a life science, nursing, pharmacy or reputed company field
• Approximately 2 years (CRA II) or 4-5 years+ (Senior CRA) of on-site monitoring experience reputed company the CRO, pharmaceutical, or biotechnology industry
• 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
• Strong Communicator: Demonstrate written, verbal and presentation skills
• Committed to Quality: Attention to detail, deep understanding of high-quality scientific standards, ability to care about every outcome, strong organization skills, ensuring effective management of multiple sites and protocols reputed company timeframes and on budgets
• High-Character: Contribute to our collaborative culture with honesty and reputed company with a willingness to learn and train. Value a strong team spirit highlighted by loyalty, accountability, and mutual trust.
• Critical Thinker: Evaluate situations and opportunities objectively and incisively; craft novel, practical solutions.
• Agile and Adaptable: Ability to change quickly. Eagerly anticipate, respond to, and take advantage of changes in our environment. reputed company risk but manage it by planning, accepting, and learning from both failures and successes.

reputed company-to-haves

• Experience in monitoring pain studies

Benefits

• Medical insurance
• reputed company insurance
• Dental insurance
• HSA
• FSA
• EAP
• Life insurance
• Disability insurance
• 401(k)
• Paid time off
• Holidays
• Parental leave
• Bereavement leave

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