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ProPharma Group Freelance GCP Consultant (REF7278P) in Stockholm, Sweden

Due to an increase in projects, we are looking for freelance GCP consultants who can support us. As a GCP consultant with ProPharma Group, you will contribute to improving or establishing the clients’ GCP compliance by providing them with the best possible advice and support. As an Auditor GCP, you work on projects as project manager, consultant (advising clients on the best possible GCP strategy) or (Lead) Auditor. In these roles, you need in-depth knowledge of GCP and EU and US legislation related to clinical trials, a good understanding of clinical product development and clinical trial organization, good communication skills, persistence and a flexible working attitude.

Qualified candidates must have:

  • Bachelors, Masters or PhD degree;

  • At least 5 years of experience within a GCP environment;

  • At least 3 years of experience within an international GCP quality assurance role, including leading of different types of audits on a regular basis;

  • Good communication skills and interpersonal skills;

  • Client-oriented, dedicated, flexible, proven project management skills and able to quickly switch between different assignments;

  • Good understanding of, Annex 11 and 21 CFR Part 11;

  • Good understanding of GMP, GLP, GVP and/or GAMP is a strong preference;

  • Leadership, authoritative and ability to remain objective in difficult situations;

  • Ability to switch easily between details and the bigger picture;

  • Adequate time and project management skills;

  • Excellent in English language;

  • Flexible to travel on, in principle, a global basis (up to around 40%).

All candidates must be legally eligible to work in the EU.

ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.