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About the role
Key responsibilities & impact- Conduct literature searches and reviews;
- Draft and/or review clinical protocols and supplementary documents for bioequivalence / relative bioavailability studies;
- Prepare the complete project dossier for submission to the CEP/Conep system via Plataforma Brasil;
- Prepare amendments, notifications or responses to queries issued;
- Prepare interim and final study reports;
- Contribute technical responses to requirements issued by the competent authorities;
- Stay up to date with applicable regulations and technical requirements.
Requirements
What you’ll need- Bachelor's degree in Pharmacy, Biology, Biotechnology or related fields.
- Strong communication skills, literature research, and technical and scientific writing;
- Intermediate to advanced English.
Benefits
Comp & perks- Transportation allowance;
- Parking (subject to availability);
- Health plan with no monthly premium cost to the employee, with copayments for tests and consultations;
- Dental plan with copayments;
- Life insurance at no cost to the employee;
- Flexible meal/food allowance;
- SESC partnership;
- Physical wellness program - TotalPass;
- Day off – health professional;
- Childcare assistance (according to internal policy).
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
literature searchesclinical protocolsbioequivalence studiesrelative bioavailability studiesproject dossier preparationamendments preparationstudy reportstechnical responsesregulatory compliancescientific writing
Soft Skills
communication skillsliterature researchtechnical writingscientific writing