Job Description

• Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
• We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description

Responsibilities:

• The Senior Manager, Regulatory CMC Technical Writing and Submission Management role will be responsible for supporting the authoring, compiling and management of CMC sections for global regulatory filings.
• This role requires a strong understanding of the drug development process, pharmaceutical technology, and regulatory requirements, while collaborating with cross-functional teams to meet technical writing and submission management objectives.
• Support the CMC regulatory writing for high-quality and compliant regulatory CMC documentation (e.g., INDs, CTAs, MAAs, NDAs and their amendments/variations/supplements, as applicable) within defined timelines.
• Support Regulatory CMC submission management.
• Support determination of regulatory and scientific/technical requirements for CMC submissions.
• Maintain knowledge of CMC regulatory requirements for drug development through post-approval and annual updated.

Requirements:

• BS in Chemistry, Pharmaceutical Sciences, Regulatory Affairs or other relevant fields.
• 3 - 5 years of experience in authoring CMC sections of regulatory filings.
• Demonstrated competency in clear and concise technical writing ability.
• Understanding of CMC manufacturing documentation requirements.
• Experience with regulatory submissions and requirements, including eCTD documents required for INDs, NDAs and MAAs, supplements and briefing documents.
• Ability to read and interpret regulations and guidance.
• Excellent team interaction skills and ability to work successfully in a cross-functional team.
• Ability to work in a dynamic environment with a high degree of flexibility.
• Independent management of projects.
• Well organized, flexible, and able to communicate effectively within CMC functions and Regulatory affairs, both spoken and in writing.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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