Current job openings
We are only as good as our team. Thus, at Viridbio Solutions, meeting your career needs is our top priority. We provide an environment that enables our team members to grow and challenge themselves. We are always looking for the right candidates in the research and development (non-clinical, preclinical, clinical), biometrics (biostats, clinical programming, data management, data operations), medical writing, and information technology. Please submit your resume at jobs@viridbiosolutions.com and our career experts will work with you to identify the best path for your career.
Medical Writer (multiple positions)
Candidate should have strong background in regulatory writing. The writer should have written multiple regulatory documents such as protocols, CSRs, IBs, DSURs, briefing books, submission documents etc. Writer with a broad experience across all clinical phases are required. Writers with strong experience in Phase 1 documents are highly encouraged.
Education and Experience Requirements/Qualifications:
• Advanced degree in a relevant scientific/clinical/regulatory field preferred
• At least 5 years of pharmaceutical industry experience in the clinical/regulatory field
• Global regulatory submission experience.
• Excellent writing skills.
• Ability to understand and interpret clinical and scientific data; ability to present results in an understandable manner to a variety of audiences.
• Knowledge of current requirements and guidelines applicable to submission documents
• Excellent interpersonal and oral communication skills.
• Strong knowledge of MS Word, Excel, PowerPoint, and Outlook
• Ability to prioritize multiple projects
Please submit your resume at jobs@viridbiosolutions.com
Medical Writer (multiple positions)
Candidate should have strong background in regulatory writing. The writer should have written multiple regulatory documents such as protocols, CSRs, IBs, DSURs, briefing books, submission documents etc. Writer with a broad experience across all clinical phases are required. Writers with strong experience in Phase 1 documents are highly encouraged.
Education and Experience Requirements/Qualifications:
• Advanced degree in a relevant scientific/clinical/regulatory field preferred
• At least 5 years of pharmaceutical industry experience in the clinical/regulatory field
• Global regulatory submission experience.
• Excellent writing skills.
• Ability to understand and interpret clinical and scientific data; ability to present results in an understandable manner to a variety of audiences.
• Knowledge of current requirements and guidelines applicable to submission documents
• Excellent interpersonal and oral communication skills.
• Strong knowledge of MS Word, Excel, PowerPoint, and Outlook
• Ability to prioritize multiple projects
Please submit your resume at jobs@viridbiosolutions.com