Iovance Biotherapeutics

Regulatory Affairs CMC Associate II

Iovance Biotherapeutics · Remote

Posted about 3 months ago

or apply directly on Iovance Biotherapeutics's site. We never take the application ourselves.

Is this posting real?

This role has been open
82 days
Iovance Biotherapeutics's roles stay open a median of 83 days
Reposted
No
Salary listed
No
0% of Iovance Biotherapeutics's roles list one
Ghost-job risk at Iovance Biotherapeutics
high
43 stale, 1 reposted of 43 open
Hiring momentum
69 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-10-25

Measured from postings appearing on and disappearing from Iovance Biotherapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Iovance Biotherapeutics.

About this role

The Regulatory Affairs CMC Associate II at Iovance Biotherapeutics will be responsible for planning and managing regulatory submissions related to CMC dossier content for clinical and commercial applications. This role involves preparing submission documents, maintaining regulatory files, and ensuring compliance with eCTD specifications. The associate will also facilitate communication with vendors and CROs, support regulatory strategy implementation, and collaborate with internal teams to ensure timely and high-quality submissions.

Our read on this posting2.0out of 5
benefits
1/5
freshness
1/5
career value
4/5
role clarity
4/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Iovance Biotherapeutics as an employer.

What you need

  • BS degree required; advanced degree (PharmD, PhD, Master’s) preferred
  • Minimum 5 years’ experience in regulatory affairs or a related function in drug/biologic development
  • Experience in managing regulatory submissions for investigational or marketed products to global health authorities in eCTD format
  • Understanding of US and international regulations and procedures in drug/biologics development
  • Familiarity with ICH eCTD structure and major market post-approval change requirements
  • Advanced skills in using Microsoft Office Suite and Adobe Acrobat Pro

What you get

  • Annual base salary range of $120,000 — $140,000 USD

Worth weighing

  • Remote work environment requires self-management of workspace
  • Fast-paced small company environment may lead to changing priorities
  • No specific mention of additional benefits or perks beyond salary

Summarised from Iovance Biotherapeutics's posting. Read the full original.

Listed by Iovance Biotherapeutics on their greenhouse job board, last confirmed open on 2026-10-25. PitchMeAI is not the employer.

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