refresh

Trending companies

Trending companies

Thermo Fisher
Thermo Fisher

Ctry Approval Spec at Thermo Fisher

RoleLegal
LevelMid Level
LocationArgentina
WorkRemote
TypeFull-time
Posted3 days ago
Apply now

About the role

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

  • Prepares, reviews and coordinates, under guidance, regulatory submissions to EU CTIS ( and additional special national local applications if applicable, e.g. gene therapy approvals) in alignment with global submission strategy;

  • Provides, under guidance local regulatory strategy advice (MoH &/or EC) to internal clients;

  • May have contact with investigators for submission related activities;

  • Key-contact at country level for either Ethical or Regulatory submission-related activities;

  • Coordinates, under guidance, with internal functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed upon timelines; ensures alignment of submission process for sites and study are aligned to the critical path for site activation;

  • Achieves PPD’s target cycle times for site;

  • May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable;

  • May develop country specific Patient Information Sheet/Informed Consent form documents;

  • Enters and maintains trial status information relating to start up activities onto PPD tracking databases in an accurate and timely manner;

  • Ensures the local country study files and filing processes are prepared, set up and maintained as per PPD WPDs or applicable client SOPs;

  • Maintains knowledge of and understand PPD SOPs, Client SOPs/directives, and current regulatory guidelines as applicable to services provided.

Qualifications: Education and Experience:
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years).

Working Conditions and Environment:

  • Work is performed in an office/ laboratory and/or a clinical environment.
  • Exposure to biological fluids with potential exposure to infectious organisms.
  • Exposure to electrical office equipment.
  • Personal protective equipment required such as protective eyewear, garments and gloves

Required skills

Regulatory submissions

Clinical research

Documentation

Coordination

Strategy

About Thermo Fisher

Remote

Headquarters