Immunocore
Key Responsibilities
The Director, Medical Writing will lead document strategy, overseeing authoring, review processes, and writing assigned documents. They will coordinate internal and external writers, establish best practices for high-quality preclinical summaries, clinical, and regulatory submission documents, ensuring compliance with ICH/GCP/regulatory guidelines for global health authority submissions such as IND/CTA/BLA. Lead planning, authoring, and review of regulatory documents
(e.g., Protocols, CSRs, IBs, briefing documents). Evaluate and review documents
generated by internal and external writers for consistency, formatting, and scientific accuracy. Engage with external stakeholders
including vendors and thought leaders as needed. Manage timelines
for document development and approvals. Assess medical writing needs
and ensure resources are adequate for timely completion. Oversee document management
from draft to final version, including review coordination and style adherence. Support development and improvement of best practices, SOPs, and templates. Lead matrix teams
effectively. Maintain a track record of developing high-quality scientific and regulatory documents
such as protocols, study reports, and responses to regulatory questions. Deep knowledge of drug/biologic development and GxP principles. Strong leadership, planning, and project management skills . Collaborate effectively
to resolve comments and meet deliverables. Manage multiple projects
in a fast-paced environment, adaptable to changing priorities. Excellent communication skills
and attention to detail. Self-motivated
with the ability to work independently. Proficiency in Microsoft Office and electronic document management systems. Experience responding to audits. Educational background : Bachelor’s in a scientific discipline; advanced degrees preferred. Experience : 8-12 years (Bachelor's level) or 6-8 years (advanced degree) in medical/scientific writing within pharma/biotech. #LI-REMOTE About the Company
Immunocore (NASDAQ: IMCR) is a pioneering T cell receptor biotechnology company focused on developing transformative medicines for oncology, infectious diseases, and autoimmune conditions. Our R&D leaders are recognized globally for success in drug development. We foster an innovative environment dedicated to delivering first-in-class biological therapies using our soluble TCR platform, including ImmTAX molecules that harness the immune system to treat diseases with high unmet medical needs. At Immunocore, we value our employees and embrace our core principles of Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE). We are committed to creating an inclusive workplace where everyone is valued, respected, and empowered. We encourage applications from individuals of all backgrounds, supporting our mission to develop breakthrough therapies and transform patients’ lives.
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The Director, Medical Writing will lead document strategy, overseeing authoring, review processes, and writing assigned documents. They will coordinate internal and external writers, establish best practices for high-quality preclinical summaries, clinical, and regulatory submission documents, ensuring compliance with ICH/GCP/regulatory guidelines for global health authority submissions such as IND/CTA/BLA. Lead planning, authoring, and review of regulatory documents
(e.g., Protocols, CSRs, IBs, briefing documents). Evaluate and review documents
generated by internal and external writers for consistency, formatting, and scientific accuracy. Engage with external stakeholders
including vendors and thought leaders as needed. Manage timelines
for document development and approvals. Assess medical writing needs
and ensure resources are adequate for timely completion. Oversee document management
from draft to final version, including review coordination and style adherence. Support development and improvement of best practices, SOPs, and templates. Lead matrix teams
effectively. Maintain a track record of developing high-quality scientific and regulatory documents
such as protocols, study reports, and responses to regulatory questions. Deep knowledge of drug/biologic development and GxP principles. Strong leadership, planning, and project management skills . Collaborate effectively
to resolve comments and meet deliverables. Manage multiple projects
in a fast-paced environment, adaptable to changing priorities. Excellent communication skills
and attention to detail. Self-motivated
with the ability to work independently. Proficiency in Microsoft Office and electronic document management systems. Experience responding to audits. Educational background : Bachelor’s in a scientific discipline; advanced degrees preferred. Experience : 8-12 years (Bachelor's level) or 6-8 years (advanced degree) in medical/scientific writing within pharma/biotech. #LI-REMOTE About the Company
Immunocore (NASDAQ: IMCR) is a pioneering T cell receptor biotechnology company focused on developing transformative medicines for oncology, infectious diseases, and autoimmune conditions. Our R&D leaders are recognized globally for success in drug development. We foster an innovative environment dedicated to delivering first-in-class biological therapies using our soluble TCR platform, including ImmTAX molecules that harness the immune system to treat diseases with high unmet medical needs. At Immunocore, we value our employees and embrace our core principles of Science, Trust, Respect, Integrity, Diversity, and Entrepreneurship (STRIDE). We are committed to creating an inclusive workplace where everyone is valued, respected, and empowered. We encourage applications from individuals of all backgrounds, supporting our mission to develop breakthrough therapies and transform patients’ lives.
#J-18808-Ljbffr