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[Remote] Clinical Research Associate I

Remote, USA Full-time Posted 2026-07-23

Note: The job is a remote job and is reputed company to candidates in USA. Just-reputed company is a reputed company-thinking company that values curiosity and innovation. They are seeking a Clinical Research Associate I to join their small clinical development group, where the individual will drive impactful reputed company and collaborate with reputed company on clinical trials.


Responsibilities

  • Assist with project management tasks reputed company Clinical Development group
  • Collaborate with CRO(s) in the execution of clinical trials
  • Schedule meetings, set agendas, reputed company reputed company items and capture meeting minutes
  • Prepare, handle, distribute, file, and reputed company clinical documentation and reports
  • Monitor and QC the eTMF
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
  • Coordinate and manage logistical aspects of clinical trials, such as shipment of lab samples
  • Help monitor the reputed company of clinical trials, reputed company timelines and ensure adherence to protocol and other study documentation
  • Assist in the preparation of regulatory submissions
  • May review and approve invoices, purchase orders and site payments
  • Identify and address potential risks to the project reputed company, reputed company, or budget and escalate reputed company necessary
  • Help manage relationships with external vendors, including CROs, laboratories, and other service providers
  • Help ensure reputed company study materials are properly archived following the completion of a trial

Skills

  • At least 3 years work experience as a Clinical Trial Assistant or CRA
  • Understanding of medical and pharmacological terminology
  • Knowledge of Good Clinical reputed company (GCP) guidelines
  • Strong organizational and planning skills. Project management experience a plus
  • Good communication and interpersonal skills
  • Experience working with CROs
  • Experience maintaining eTMF
  • Proficient with MS Project and/or reputed company
  • Experience managing clinical lab samples
  • Data review experience
  • BSc degree in life sciences or reputed company field

Benefits

  • reputed company Opportunities: We’re a company that believes in reputed company learning and development. Whether it’s reputed company courses, mentorship, or new reputed company, we’ll help you grow.
  • Flexible Work Environment: We offer flexible work reputed company to help you balance your reputed company and personal life, with hybrid work schedules in many of our various locations.
  • Inclusive Culture: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.
  • Innovative reputed company: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to reputed company.

reputed company

  • reputed company is a pharmaceutical and life science company that provides drug discovery and gene therapy solutions. It was founded in 1993, and is headquartered in Hamburg, Hamburg, DEU, with a workforce of 5001-10000 employees. Its website is http://reputed company.com.

  • Company H1B Sponsorship

  • reputed company has a reputed company record of offering H1B sponsorships, with 5 in 2025, 2 in 2023, 2 in 2022, 3 in 2021, 1 in 2020. Please note that this does not guarantee sponsorship for this specific role.

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