Specialist, Clinical Development (CSD)
Singapore, SG
3d ago

The Medical Affairs team collaborates with the leaders of Sleep, Respiratory Care, SaaS, ResMed Healthcare, and Asia Growth Markets to ensure our work, especially our clinical research and market access projects, align with their strategic priorities.

We also review key government policies, as part of the continuous evaluation and improvement process that helps us maintain global compliance across an ever-shifting landscape of legal and regulatory requirements.

The two, research and compliance, work hand-in-hand, and when balanced properly allow us to generate important clinical, economic and market evidence, that improves the lives of patients in ways that are scientifically valid, clinically relevant and ethically sound.

Let's talk about the team and you

This role is in the medical affairs team to support our growth in the APAC region. The role reports to our Medical Affairs, Senior Manager for Respiratory Care and will be responsible for managing the clinical development of new products as well as planning, development, and implementation of clinical research across the business.

Let's talk about Responsibilities

  • To provide clinical input into global product development across to ensure the safety, efficacy, and usability of ResMed products.
  • Research, make recommendations and manage clinical related studies, usability evaluations and clinical trials as required.
  • Liaise with client groups (Product Development, Marketing, Regulatory, Clinical Science and Innovation) to provide clinical support.
  • Provide clinical input to support the ongoing life of existing products (ie. risk assessments, field complaints, marketing material).
  • Develop white papers, conference posters, journal papers, and other scientific literature.
  • Develop training materials and facilitate specialised clinical and medical educational sessions for the business.
  • Be the Medical Affairs representative on product development teams, with responsibility of delivering on MA requirements for project XFT.
  • Perform clinical trial site management duties (ie. Site selection, start-up, monitoring) as required.
  • Let's talk about Qualifications and Experience

  • Minimum Bachelor Degree in Medical Science, Science or Health Sciences.
  • Postgraduate qualifications and / or therapeutic area knowledge in the Respiratory Care Therapy Area desirable.
  • 3-5 years of working experience in a clinical / patient care environment (nursing, respiratory therapist, pulmonary rehab etc) OR clinical product development.
  • Added experience in clinical research (in areas such as conducting and monitoring clinical trials, clinical input into product development etc) is a good advantage.

  • Experience in managing stakeholders from cross functional teams.
  • Highly organized with good time management.
  • LI-IB1

    Joining us is more than saying yes to making the world a healthier place. It’s discovering a career that’s challenging, supportive and inspiring.

    Where a culture driven by excellence helps you not only meet your goals, but also create new ones. We focus on creating a diverse and inclusive culture, encouraging individual expression in the workplace and thrive on the innovative ideas this generates.

    If this sounds like the workplace for you, apply now!

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