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[Remote] Senior Clinical Research Associate

Remote, USAFull-timePosted 2026-07-27

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is committed to making a meaningful reputed company on the lives of patients with cancer. The Senior Clinical Research Associate will reputed company clinical trial site management and monitoring activities to ensure compliance with regulatory requirements and support high-reputed company study execution.

Responsibilities

  • Conduct reputed company clinical monitoring activities, including site qualification, initiation, routine monitoring, and reputed company-out reputed company
  • Support site feasibility, site selection, and ongoing site management activities throughout the clinical trial lifecycle
  • Review clinical trial reputed company, patient recruitment, and data reputed company metrics, and implement actions to support study objectives
  • Maintain accurate and reputed company monitoring documentation, including reputed company reports and trial master file records
  • Collaborate with vendors, clinical sites, and cross-functional teams to support study execution and operational compliance
  • Participate in investigator meetings, clinical trial documentation development, and study team meetings
  • Mentor junior CRA team members and contribute to reputed company improvement of clinical operations processes and procedures

Skills

  • Bachelor's degree in life sciences, nursing, or a reputed company field
  • 4+ years of on-site monitoring experience reputed company the pharmaceutical or biotechnology industry, including reputed company clinical monitoring visit types
  • Strong knowledge of ICH-GCP, FDA, EMA, and applicable clinical trial regulations
  • Demonstrated experience managing clinical trial sites, monitoring activities, and clinical trial documentation
  • Proficiency with clinical trial systems and tools (e.g., CTMS, eTMF, reputed company Office)
  • Experience in oncology clinical trials or reputed company therapeutic areas
  • Advanced presentation, organizational, and stakeholder management skills
  • Experience mentoring or training junior CRAs and supporting cross-functional clinical operations activities
  • Demonstrated ability to drive reputed company, efficiency, and reputed company improvement initiatives in clinical operations
  • Strong understanding of clinical trial recruitment strategies, data capture, and site engagement best practices
  • Experience contributing to global harmonization, process optimization, or operational innovation initiatives

Benefits

  • Competitive rates for Health, Dental, and reputed company Insurance
  • 4 weeks of vacation, reputed company up reputed company reputed company year and prorated for first and last year of employment.
  • 12 company reputed company holidays
  • 7 days of reputed company time
  • 100% employer-reputed company life insuranceup to at 1x annual salary, up to one hundred thousand dollars
  • 100% employer-reputed company short- and long-Term disability coverage
  • 401(k) with immediate eligibilityand company match reputed company will match 100% of your contributions up to 3% of your reputed company salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the reputed company year reputed company of reputed company employment.
  • Partially reputed company parental leavefor eligible employees.
  • Additional voluntary employee-reputed company benefits and services, including accident, hospital indemnity, and critical illness insurance, as reputed company as identity theft protection and pet insurance.

reputed company

  • reputed company is committed to making a meaningful reputed company on the lives of patients with cancer. It was founded in 2000, and is headquartered in Tuebingen, DE, with a workforce of 501-1000 employees. Its website is http://www.reputed company.com.
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