Freelance / Consultant 0.5 FTE Person Responsible for Local Literature Screening - Fluent in German

Posted 17 Days Ago
Be an Early Applicant
Hiring Remotely in Prague
Remote
Entry level
Biotech • Pharmaceutical
The Role
This role involves local scientific literature monitoring for adverse events, formulating search strategies, providing translations, and ensuring compliance with data privacy and security. It requires fluency in German and English and proficiency in MS Office. The position is freelance, working at 0.5 Full-Time Equivalent (FTE).
Summary Generated by Built In

Company Description

We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. 

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device. 

Job Description

This is an exciting opportuniy for a freelancer / consultant to join our team as a Person Responsible for Local Literature Screening at 0.5 FTE.

By working with us, you will have the opportunity to work in an international team.

Main responsibilities

  • Performing local scientific literature and national safety web portal monitoring for adverse event reports and other safety information in line with the applicable controlled written procedures of PrimeVigilance and client specific arrangements.
  • Formulation and/or adjustment of the search strategy: selection of search terms and identification of all applicable local equivalents to achieve the best available outcome taking into consideration the available/selected sources.
  • Providing translation or revision of any relevant documentation upon request.
  • Ensuring that files are properly maintained as per applicable PrimeVigilance procedures, and that local security and data privacy requirements are met.

Qualifications

  • Bachelor's Degree in Life Sciences, Chemistry or Nursing 
  • Fluent in English and German
  • Proficiency in all MS-Office applications including Microsoft Word, Excel, and PowerPoint
  • Must currently be set up to work as a freelancer / consultant

Additional Information

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.

To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. 

Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!

  • Quality 

  • Integrity & Trust

  • Drive & Passion

  • Agility & Responsiveness

  • Belonging 

  • Collaborative Partnerships

We look forward to welcoming your application. 

Top Skills

English
German
The Company
HQ: Raleigh, NC
535 Employees
On-site Workplace
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology.

• 1,400+ highly qualified professionals
• Global full-service CRO
• 25+ years of experience
• Therapeutic specialization in oncology
• Strong expertise in rare disease trials
• Robust clinical safety system
• Choice of leading drug safety databases

Our key services include:
• Clinical Research Services
• Pharmacovigilance
• Medical Information
• Regulatory
• Medical Writing
• Site Management
• Study Physician Support
• Biostatistics
• Patient Study Support

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