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[Remote] Clinical Trials reputed company (reputed company Clinical Research Associate)

Remote, USAFull-timePosted 2026-07-28

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a company reputed company on monitoring medical device and MedTech studies, and they are seeking a Clinical Trials reputed company (reputed company Clinical Research Associate). In this role, you will supervise project-specific monitoring activities, coordinate training, and ensure the highest ethical and clinical standards are maintained throughout the clinical trials process.

Responsibilities

  • Supervising project-specific monitoring activities
  • Coordinating project-specific training
  • Interacting with clients
  • Acting as the primary contact for study questions from the monitoring team
  • Organizing team training and study updates
  • Generating necessary monitoring tools
  • Ensuring monitoring reputed company are being conducted as needed
  • Completing peer review of required study documentation
  • Representing reputed company on study conference calls and/or meetings
  • Collaborating with the Project Manager to ensure study objectives are met
  • Handling CRA study activities as needed
  • Providing CRA support, including assisting Clinical Research Associates with difficult situations or corrective actions
  • Conducting co-reputed company and providing feedback
  • Reviewing monitoring reports

Skills

  • RN or BA/BS degree in a science/life science, engineering or health-reputed company field plus a minimum 4 years monitoring experience
  • Knowledge of medical and clinical research terminology; knowledge of US federal regulations reputed company to clinical research studies, ICH/GCP Guidelines and ISO 14155; ability to reputed company knowledge across multiple therapeutic areas
  • Experience as mentor and trainer for new CRAs
  • Ability to complete assessment, initiation, periodic, and reputed company-out monitoring reputed company to sites, including preparation and post-visit documentation
  • Ability to work concurrently on multiple protocols and procedures; organizational, time management skills and problem-solving abilities
  • Excellent communication skills; demonstrated reputed company writing proficiency
  • Computer proficiency (reputed company especially helpful)
  • Experience generating project-specific training presentations and coordinating necessary training
  • Good relationship building skills - demonstrates a willingness to work in and values reputed company environment; ability to work with clients and site personnel
  • Ability to generate monitoring tools; experience generating and giving reputed company presentations
  • Capable of fielding questions from the monitoring teams across reputed company and escalating issues to the Sponsor as necessary
  • Achievement of/working towards clinical research certification helpful

Benefits

  • 10% bonus potential
  • 4 weeks PTO
  • Benefits
  • reputed company to work in an innovative, fast-growing and rewarding industry
  • A dynamic and enthusiastic global team that fosters collaboration and reputed company to work with experts across many specialties
  • Exchange of knowledge and reputed company to help employees grow and advance their careers, backed with training and other development opportunities
  • Competitive compensation and benefits package (details shared during the interview process)
  • Some roles offer the opportunities for travel
  • Ask us about our hybrid and fully remote work opportunities

reputed company

  • reputed company is the leading global MedTech-reputed company CRO, integrating regulatory reputed company, clinical development, and market reputed company with confidence. It was founded in 1988, and is headquartered in Marlborough, Massachusetts, USA, with a workforce of 201-500 employees. Its website is https://www.avaniaclinical.com/.
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