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Regulatory Affairs Associate II

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 
New Jersey (USA), United States

Offer summary

Qualifications:

Familiarity with data entry into complex systems, Experience with web-based EDC and data management, Experience with Veeva Vaults, Preferred experience with RIM Vault, Strong verbal and written communication skills.

Key responsabilities:

  • Enter and maintain product information
  • Support RA CMC team to meet deliverables
  • Ensure completeness and consistency of data
  • Support enhancements to information systems
  • Develop required system skills and knowledge
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
See more Katalyst HealthCares & Life Sciences offers

Job description

Responsibilities:
  • Perform data entry using Gilead Information Systems to enter and maintain relevant product information to support cross-functional stakeholders.
  • Work collaboratively to support the RA CMC team to meet deliverables and timelines by executing routine data entry, quality control of that data entry and associated reports.
  • Ensure completeness, correctness and consistency of data and data structure.
  • Responsible for supporting project work for enhancements to information. systems for RA CMC and stakeholders who utilize RA CMC data.
  • Responsible for development and acquisition of required system skills and knowledge; training supported by manager and peers.
  • Work is performed under the general supervision of more senior Regulatory Affairs CMC Systems professionals.

Requirements:

  • Should have familiarity with data entry into complex information systems.
  • Should have familiarity with web-based Electronic Data Capture EDC and data management systems.
  • Should have experience with Veeva Vaults, experience with the RIM Vault preferred.
  • Strong verbal and written communication skills and interpersonal skills.
  • Excellent organization skills and ability to work on multiple concurrent projects with tight timelines are required.

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Verbal Communication Skills
  • Organizational Skills
  • Quality Control
  • Collaboration

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