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Ctry Approval Assoc

Thermo Fisher Scientific

Healthcare Jobs

Ctry Approval Assoc

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

• Prepares, reviews and coordinates, under guidance and local EC submissions in alignment with global submission strategy. 
• Supports preparation, under guidance, of local MoH submissions, as applicable in alignment with global submission strategy.
• 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 have contact with investigators for submission related activities.
• May act as a key-contact at country level for either Ethical or Regulatory 
submission-related activities.
• Works with the start-up CRA(s) to prepare the regulatory compliance review 
packages, as applicable.
• Assists in developing country specific Patient Information Sheet/Informed 
Consent form documents.
• Assists with grant budgets(s) and payment schedules negotiations with sites.
• Enters and maintains trial status information relating to SIA activities onto PPD, 
or client (where contracted) 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 0 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.

Locations

  • Remote, Argentina (Remote)

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Knowledge of PPD SOPs, Client SOPs, and regulatory guidelinesintermediate
  • Database entry and maintenanceintermediate
  • Filing and document managementintermediate

Required Qualifications

  • Bachelor's degree or equivalent (experience)
  • 0-2 years of relevant experience (experience)

Responsibilities

  • Prepares, reviews and coordinates local EC submissions
  • Supports preparation of local MoH submissions
  • Coordinates with internal departments for site start-up activities
  • Assists in developing country specific Patient Information Sheet/Informed Consent forms
  • Assists with grant budgets and payment schedules negotiations
  • Maintains trial status information in tracking databases
  • Ensures local country study files are prepared and maintained

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Thermo Fisher Scientific logo

Ctry Approval Assoc

Thermo Fisher Scientific

Healthcare Jobs

Ctry Approval Assoc

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

• Prepares, reviews and coordinates, under guidance and local EC submissions in alignment with global submission strategy. 
• Supports preparation, under guidance, of local MoH submissions, as applicable in alignment with global submission strategy.
• 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 have contact with investigators for submission related activities.
• May act as a key-contact at country level for either Ethical or Regulatory 
submission-related activities.
• Works with the start-up CRA(s) to prepare the regulatory compliance review 
packages, as applicable.
• Assists in developing country specific Patient Information Sheet/Informed 
Consent form documents.
• Assists with grant budgets(s) and payment schedules negotiations with sites.
• Enters and maintains trial status information relating to SIA activities onto PPD, 
or client (where contracted) 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 0 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.

Locations

  • Remote, Argentina (Remote)

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Knowledge of PPD SOPs, Client SOPs, and regulatory guidelinesintermediate
  • Database entry and maintenanceintermediate
  • Filing and document managementintermediate

Required Qualifications

  • Bachelor's degree or equivalent (experience)
  • 0-2 years of relevant experience (experience)

Responsibilities

  • Prepares, reviews and coordinates local EC submissions
  • Supports preparation of local MoH submissions
  • Coordinates with internal departments for site start-up activities
  • Assists in developing country specific Patient Information Sheet/Informed Consent forms
  • Assists with grant budgets and payment schedules negotiations
  • Maintains trial status information in tracking databases
  • Ensures local country study files are prepared and maintained

Target Your Resume for "Ctry Approval Assoc" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Ctry Approval Assoc. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Ctry Approval Assoc" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Ctry Approval Assoc @ Thermo Fisher Scientific.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.