[Remote] Country Approval Specialist - FSP Dedicated - EMEA at Thermo Fisher Scientific

France

Apply Now

Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, Pharmaceuticals, BiotechnologyIndustries

Requirements

Bachelor's degree or equivalent and relevant formal academic/vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (or equivalency consisting of a combination of appropriate education, training and/or directly related experience)
Effective oral and written communication skills
Excellent interpersonal skills
Strong attention to detail and quality of documents

Responsibilities

Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy
Provides, under guidance, local regulatory strategy advice (MoH and/or EC) to internal clients
Provides project specific local SIA services and coordination of these projects
Serves as key-contact at country level for either Ethical or Regulatory submission-related activities (may have contact with investigators for 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
May assist with grant budgets(s) and payment schedules negotiations with sites
Supports the coordination of feasibility activities, as required, in accordance with agreed timelines
Enters and maintains trial status information relating to SIA 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 understands PPD SOPs, Client SOPs/directives, and current regulatory guidelines as applicable to services provided

Skills

Key technologies and capabilities for this role

regulatory submissionsMoH approvalsEC submissionscountry submissionsclinical trialsregulatory strategygene therapy approvalsimport licensedocument reviewattention to detail

Questions & Answers

Common questions about this position

What is the work arrangement or location policy for this role?

This is a full-time position with a standard Monday-Friday work schedule in an office environment.

What are the essential functions of the Country Approval Specialist role?

Key responsibilities include preparing, reviewing, and coordinating local regulatory submissions, providing local regulatory strategy advice, coordinating site start-up activities, and achieving target cycle times for sites.

What skills or qualities are important for this position?

A strong attention to detail, ability to take ownership of document accuracy, and holding yourself and others accountable are essential.

What is the company culture like at Thermo Fisher Scientific?

The company emphasizes meaningful work with positive global impact, providing resources for career goals, and a collaborative environment focused on enabling customers to make the world healthier, cleaner, and safer through clinical research.

What makes a strong candidate for the Country Approval Specialist role?

Candidates with determination to deliver quality and accuracy, experience in regulatory submissions, and the ability to coordinate with internal teams and investigators under guidance will stand out.

Thermo Fisher Scientific

Provides life sciences products and services

About Thermo Fisher Scientific

Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.

Waltham, MassachusettsHeadquarters

1956Year Founded

$17MTotal Funding

IPOCompany Stage

Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Increased competition in single-use bioprocessing may impact market share.

Sale of anatomical pathology business could create a temporary product gap.

Investment in miDiagnostics may face regulatory challenges affecting returns.

Differentiation

Thermo Fisher offers a comprehensive range of life sciences products and services.

Their well-known brands include Thermo Scientific, Applied Biosystems, and Invitrogen.

They provide strong customer support and educational resources to optimize client workflows.

Upsides

Expansion of biologics production facility enhances capacity for precision biologics monitoring.

Investment in miDiagnostics aligns with demand for rapid diagnostic solutions in BioPharma.

Collaboration with Mainz Biomed positions them in the growing cancer detection market.

Land your dream remote job 3x faster with AI

Try Jobo Free