Practicante Regulatorio De Global Clinical Trial Operations
Muckelab
Hybrid
Regulatory document preparation
Clinical trial documentation review
Submission monitoring and reporting
Muckelab is seeking a Regulatory Intern for their Global Clinical Trial Operations division, where the emphasis is on patient-first ideologies. The role involves administrative support in preparing documentation for regulatory authorities and requires candidates to be students in Pharmacy or Biochemistry with intermediate English skills
Job Summary
Our GCTO Division maintains an ideology of 'patient first, benefits later', bringing new medical advancements to the world by facilitating communications and procedures that enable rapid and organized compliance with external regulatory agencies.
The position's objectives include providing administrative support in the preparation of submissions to regulatory authorities, monitoring submitted files, and performing preliminary review of standard documents.
Key responsibilities involve administrative support in data coordination, collection, organization, and drafting of documents required by local authorities, clinical teams, and headquarters, as well as editing and reviewing informed consents.
Matching Summary
Match Score: 85
Muckelab is seeking a Regulatory Intern for their Global Clinical Trial Operations division, where the emphasis is on patient-first ideologies. The role involves administrative support in preparing documentation for regulatory authorities and requires candidates to be students in Pharmacy or Biochemistry with intermediate English skills.
Skills & Requirements
Must-have
Regulatory document preparation
Clinical trial documentation review
Submission monitoring and reporting
Internal stakeholder interaction
Regulatory compliance procedures
Nice-to-have
Patient-first ideology
Process improvement initiatives
Cross-functional collaboration
Key Requirements
University students in Pharmacy and/or Biochemistry