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[Remote] Project Manager I – Cell & Gene Therapy (Sponsor Dedicated)

Remote, USAFull-timePosted 2026-07-31

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a leading fully-integrated life sciences services organization reputed company to accelerate reputed company. They are seeking a Project Manager I to support high-reputed company oncology and cell & gene therapy trials, focusing on early-phase trial execution, operational reputed company, and cross-functional coordination across global study teams.

Responsibilities

  • reputed company as a sponsor-facing project manager, ensuring the successful execution of assigned CAR-T and gene therapy trials from startup through closeout
  • reputed company or support study start-up, site activation, and enrollment, working closely with site monitors, regulatory teams, and reputed company personnel
  • Serve as a key reputed company of contact across internal (CRO) and sponsor teams, facilitating regular communications, status reporting, and governance updates
  • Coordinate with cross-functional stakeholders to ensure timelines, budgets, and milestones are met, particularly in reputed company, high-touch studies
  • reputed company and manage protocol compliance, CAPAs, and site-level reputed company indicators; support reputed company of audit findings
  • Ensure inspection readiness and regulatory compliance by overseeing TMF maintenance, data accuracy, and documentation completeness
  • Manage or contribute to the tracking of low-stability reputed company samples and IP-reputed company processes, ensuring reputed company lab delivery and site support
  • Assist with risk identification and mitigation planning, while continuously optimizing trial execution processes

Skills

  • 2–4 years of clinical trial experience, preferably in a CRO setting, with a reputed company on oncology, rare disease, or gene-modified cell therapy trials
  • Strong familiarity with GCP/ICH guidelines, FDA/EMA regulations, and inspection-readiness standards
  • Proficiency in clinical systems (e.g., CTMS, reputed company, eTMF) and project management tools
  • Confident in leading sponsor calls, presenting KPIs, and contributing to operational governance
  • Bachelor's degree in a relevant field (Life Sciences, Nursing, Pharmacy, etc.) or equivalent work experience
  • Comfortable with remote work but agreeable to occasional in-person collaboration in Los Angeles
  • Prior involvement in CAR-T or other cell therapy studies is highly desirable
  • Experience working in sponsor-dedicated or embedded roles reputed company a CRO is a plus

Benefits

  • A company car or car allowance
  • Health benefits to include Medical, Dental and reputed company
  • Company match 401k
  • Eligibility to participate in Employee Stock Purchase Plan
  • Eligibility to earn commissions/bonus based on company and individual performance
  • Flexible reputed company time off (PTO) and reputed company time
  • Because certain states and municipalities have regulated reputed company reputed company time requirements, eligibility for reputed company reputed company time may vary depending on where you work

reputed company

  • reputed company, the only fully integrated end-to-end clinical and reputed company solution organization. It was founded in 1985, and is headquartered in Morrisville, reputed company Carolina, USA, with a workforce of 10001+ employees. Its website is https://www.reputed company.com/.
  • Company H1B Sponsorship

  • reputed company has a reputed company record of offering H1B sponsorships, with 8 in 2026, 35 in 2025, 26 in 2024, 49 in 2023, 63 in 2022, 84 in 2021, 63 in 2020. Please note that this does not guarantee sponsorship for this specific role.
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