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Amylyx

Director, IT R&D and Quality Applications

RemoteUnited States, United Kingdom, Canada +1 more only· Prefers United Kingdom
Published
Role
Engineering Management
Experience
Lead
Employment
Full-time
$206k–$232k/yr
Check eligibility

Open to US, GB, CA, NZ only · Prefers United Kingdom. Set where you work from to check your eligibility.

The listing prefers candidates in United Kingdom.

No BS summary

Director-level IT leader for life sciences R&D/clinical/quality applications with 10+ years in business applications and 5+ years implementing R&D/Clinical Systems. Must know clinical trial systems, Veeva Vault R&D Suite, GxP/21 CFR Part 11, clinical data integrations, and SaaS vendor management. US remote only, excluding AK, AZ, HI, MI, and TN; New England/Cambridge access preferred.

Core skills

Veeva Vault R&D SuiteGxPClinical Trial Systems

Required skills

CTMSeTMFeCROePROICH E6(R3)21 CFR Part 11ALCOA+CDISCSDTMADaMComputer System AssuranceSaaS

Optional skills

EDCCDB

What you'll do

  • Serve as the lead IT partner across Clinical Operations, Data Management, Biometrics.
  • Oversee systems supporting regulatory submissions, pharmacovigilance, and quality management.
  • Support complex clinical trials involving decentralized models, subject diaries, and connected devices.
  • Lead implementation and support of R&D systems including Clinical Trial management solutions including CTMS, EDC, eTMF, ePRO/eCOA, IRT, and consolidated clinical analytics solutions.
  • Spearhead use & enablement of AI solutions within R&D, Clinical & Quality systems.
  • Develop integration strategy across clinical data ecosystems including the Veeva Vault R&D Suite and analytics environments.
  • Ensure compliance with GxP regulations including ICH E6(R3), 21 CFR Part 11, and data integrity (ALCOA+).
  • Lead technology solutioning including vendor selection, RFP processes, and vendor relationship management.
  • Manage system roadmap, budgeting, and portfolio prioritization.

What they require

  • Bachelor’s degree in computer science, Life Sciences, or related field.
  • 10+ years of Life sciences business applications experience with 5+ years implementing and supporting R&D / Clinical Systems.
  • Experience with clinical trial systems is required (CTMS, eTMF, eCRO, ePRO).
  • Preferred: Experience with clinical data management (EDC, CDB) and Biometric analytical platforms preferred.
  • Deep expertise in Veeva Vault R&D Suite (Clinical, RIM, Quality, Safety).
  • Expertise in integrating complex clinical data sources including ePRO, wearables, and medical devices.
  • Strong knowledge of GxP regulations, CDISC standards (SDTM, ADaM) and Computer System Assurance frameworks.
  • Experience managing cross-functional teams and SaaS-based vendors.
  • Excellent communication and problem-solving skills.
  • Preference will be given to candidates who reside in the New England region and can be in person on an as needed basis.
  • If outside of the New England region, you will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested, which may include travel by air, driving or public transportation.
  • When working remotely, you must have access to a work setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.

Benefits

  • Remote work opportunities within the United States.
  • Accommodations are available for candidates who require them in our selection process.

Amylyx is a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).

🇬🇧 United KingdomBiotechStartupamylyx.com/

Details

Apply routeGreenhouse
$206k–$232k/yr