Future Tech Jobs
Future Tech Jobs
This role involves leading the clinical development of a medicine, managing a cross-functional team, and ensuring high-quality clinical and scientific standards. Responsibilities include strategic leadership, clinical oversight, and authoring key study documents and regulatory submissions.
POSITION SUMMARYYou will provide clinical and scientific support for global Phase 1–4 vaccine clinical studies within the Vaccines portfolio. Working in close partnership with clinical colleagues, this role contributes to study design, clinical data review, safety oversight, and scientific integrity...
The VP, Global Medical Lead for the mRNA portfolio is responsible for shaping the global medical strategy for GSK's mRNA vaccines, including Flu, Covid, and Combination products. This role involves leading cross-functional teams, developing medical brand strategies, and ensuring that healthcare decision-makers have the necessary evidence to support GSK's therapies. The leader will also mentor their team and collaborate with key markets and internal stakeholders to optimize patient impact and advance medical practices.
The VP, Global Medical Lead for the mRNA portfolio will lead the global medical strategy for GSK's mRNA vaccines, including Flu, Covid, and Combination vaccines. They will be responsible for shaping medical practices, generating evidence, and collaborating with cross-functional teams to ensure the successful development and commercialization of these vaccines. The role involves leading a global medical team, setting strategic direction, and mentoring direct reports.
This role involves operating production equipment for mRNA vaccines, adhering to cGMP standards, and maintaining a safe, compliant working environment. The candidate will work closely with QA, troubleshoot issues, and contribute to continuous improvement in a fast-paced, technologically advanced setting.
The Manufacturing Associate I role involves operating production equipment for mRNA vaccines, adhering to cGMP standards, and maintaining a safe and compliant working environment. Responsibilities include troubleshooting equipment, participating in quality assurance, and contributing to continuous improvement projects in a fast-paced, technologically advanced setting.
The Senior Medical Affairs Manager is a key scientific leader responsible for external engagement with key opinion leaders, healthcare organizations, and policy stakeholders. The role involves developing and executing the UK Medical Affairs strategy, leading scientific exchanges, and representing Seqirus at national scientific forums. The position also focuses on internal collaboration, evidence generation, and ensuring compliance with regulatory standards.
The Quality Oversight and Compliance Director at Pfizer is responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing quality oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.
This role involves maintaining and improving CSL's global pharmacovigilance (PV) system, ensuring compliance with GVP and regulatory requirements. Responsibilities include leading investigations, managing deviations, coordinating inspections, and providing PV training across various functions and affiliates.
