_{03rd March, 2025}

THE OPPORTUNITY
We are recruiting for our client who is a fast-growing biopharmaceutical ASX-listed mid cap conducting clinical trials in globally. Their mission is to develop groundbreaking therapies that address unmet medical needs.

As the Medical Officer, you will play a pivotal role in ensuring the safety, efficacy, and regulatory compliance of their clinical programs. You will be responsible for the design and execution of clinical trials, regulatory submissions, and responding to adverse events.

This is an exciting opportunity to work in a dynamic, innovative, and collaborative environment where your expertise will directly contribute to the development of life-changing treatments.

SUCCESS LOOKS LIKE THIS

• Providing medical insights and oversight in clinical trials
  Ensure the scientific integrity and safety of clinical trials by reviewing protocols, monitoring progress, and addressing medical concerns.
• Ensuring regulatory compliance and acting as a key liaison with authorities
  Support regulatory submissions, respond to inquiries, and ensure all clinical activities align with ethical and compliance standards.
• Overseeing safety monitoring and pharmacovigilance efforts
  Evaluate adverse event reports, collaborate on risk management, and ensure patient safety throughout the trial process.
• Collaborating with clinical, regulatory, and commercial teams to align on strategy
  Work cross-functionally to integrate clinical insights into regulatory planning, market strategy, and medical affairs initiatives.
• Keeping up with scientific advancements and identifying new research opportunities
  Stay informed on emerging therapies, contribute to scientific publications, and explore opportunities for new clinical studies.
• Championing transparency, accountability, collaboration, and innovation
  Promote ethical practices, foster collaboration, and drive continuous improvement in drug development.

LET’S TALK ABOUT YOU
You are a medically qualified professional with a strong background in clinical research and pharmaceutical development. You thrive in a fast-paced, evolving environment and enjoy working with cross-functional teams.
You bring:

• Medical degree with experience in clinical practice
• Experience in pharmaceutical research and clinical trials
• Strong background in clinical trial safety oversight and pharmacovigilance
• Expertise in regulatory submissions (INDs, NDAs, CTAs)
• Strong critical thinking, problem-solving, and decision-making skills
• Excellent communication and collaboration abilities
• Ability to adapt to changing regulatory landscapes and emerging scientific data

NEXT STEPS
If you are passionate about medical innovation and want to be part of a company that is transforming biopharmaceutical research, we want to hear from you!  Please reach out to Kylie Saunders for a confidential conversation – kylie.saunders@worktrybe.com or apply below.

Apply now and take the next step in your career.

Apply For Job