Medical Director for Global Clinical Trials

4 days ago

Melbourne, Victoria, Australia beBeeClinical Full time $180 - $230
Job Overview

This role involves the development of global clinical trials, including medical oversight for all trials, portfolio and/or protocol medical feasibility, scientific engagement of investigators, protocol and TA training for internal and external stakeholders, medical issue or question management, safety review, and strategic input in pre-launch planning.

Main Responsibilities
  • Medical oversight of clinical trials across all stages and contribute to operational trial deliverables according to timelines, quality/compliance, and performance standards.
  • Drive portfolio/trial medical feasibility within the Global Development framework and provide country clinical strategic guidance and proposals in collaboration with Study and Site Operations Team and Medical Affairs Team.
  • Identify and propose new sites for clinical trials, analyse capability, assess patient pool and country treatment landscape, and make recommendations for potential trial inclusion.
  • Provide robust indication and protocol training to CRAs, CSMs, RSMs, and other functions in the country as needed.
  • Responsible for medical related education, implementation, and compliance to protocol, standards (SOPs) and best practices for clinical development within assigned clinical trial(s) and within clinical program(s), including sharing lessons learned.
  • Provide medical expertise to clinical/operational activities for patient eligibility, medical question-management, safety, amendments, etc.
  • Collaborate cross-functionally for the early product launch planning process to ensure Global Development trials conducted are aligned with the local country strategy.
  • Support medical/clinical team discussions with local regulatory interactions as needed.

The ideal candidate will have a medical degree, proven experience in medical practice or pharmaceutical industry experience with a background in clinical trials/medical affairs/life sciences/research in all aspects of drug development including clinical research, GCP, and local regulatory requirements. Experience in Haematology and Oncology clinical trials is valuable.

This role requires outstanding internal and external stakeholder engagement experience, as well as demonstrated experience in managing projects, feasibility conduct, and the execution of strategic plans from a medical perspective.

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Required Skills and Qualifications
  • Medical degree
  • Proven experience in medical practice or pharmaceutical industry experience
  • Background in clinical trials/medical affairs/life sciences/research
  • Clinical research experience
  • GCP experience
  • Local regulatory requirements experience
  • Haematology and Oncology clinical trials experience
Benefits

This role offers a challenging and rewarding opportunity to contribute to the development of global clinical trials and work with a diverse team of professionals. We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.

Others

We are an equal opportunities employer and welcome applications from candidates of all backgrounds. We are committed to creating a workplace that is inclusive, respectful, and supportive of all employees.

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