We are seeking a deep expert microbiologist to lead aspects of late‐stage development of candidate anti‐infective medicines.

Requirements

Provide strategic oversight, lead the design, oversee execution, and interpret results of microbiology studies to advance clinical development of anti-infective medicines.
Drive collaboration with cross-functional teams to develop and execute project strategies that support the overall project goals and timelines.
Manage multiple projects simultaneously, prioritize tasks, and coordinate with internal and external stakeholders to ensure timely delivery of high-quality documents and data packages.
Draw from established experience in Pharma industry to proactively foster innovation and resolve complex scientific and technical challenges.
Provide guidance and mentorship to junior scientists to ensure successful delivery of microbiology data packages.
Lead communication of study results and scientific findings through written reports, presentations, and publications.
Author high quality Regulatory Study Reports and manuscripts in peer-reviewed journals; contribute to IP patent filing and regulatory document preparation.
Ensure compliance with regulatory requirements, ethical guidelines, and GSK standards for data integrity, safety, and quality.

Benefits

We are seeking a deep expert microbiologist to lead aspects of late‐stage development of candidate anti‐infective medicines.

Provide strategic oversight, lead the design, oversee execution, and interpret results of microbiology studies to advance clinical development of anti-infective medicines.
Drive collaboration with cross-functional teams to develop and execute project strategies that support the overall project goals and timelines.
Manage multiple projects simultaneously, prioritize tasks, and coordinate with internal and external stakeholders to ensure timely delivery of high-quality documents and data packages.
Draw from established experience in Pharma industry to proactively foster innovation and resolve complex scientific and technical challenges.
Provide guidance and mentorship to junior scientists to ensure successful delivery of microbiology data packages.
Lead communication of study results and scientific findings through written reports, presentations, and publications.
Author high quality Regulatory Study Reports and manuscripts in peer-reviewed journals; contribute to IP patent filing and regulatory document preparation.
Ensure compliance with regulatory requirements, ethical guidelines, and GSK standards for data integrity, safety, and quality.