Feasibility Specialist – Auckland

2 weeks ago

Auckland, Auckland, New Zealand PCRN Ltd Full time

We're looking for a Clinical Trials Feasibility Specialist to play a key role in securing valuable clinical trials for PCRN. In this pivotal position, you'll assess trial feasibility, showcase our capabilities to sponsors and CROs, and ensure we're positioned to win and successfully execute clinical studies. If you're analytical, strategic, and passionate about bringing new treatments to patients, we'd love to hear from you

Working with us

Clinical research helps improve lives. At Pacific Clinical Research Network New Zealand, we are paving the way for the global availability of innovative medicines and treatments.

The work we do showcases New Zealand as the country of choice for medical trials. With 9 state-of-the-art partner facilities nationwide, we attract a diverse pool of participants, producing extensive high-quality data. Responsive, caring and highly trained staff ensure consistently high safety and ethical standards across our network. With centralised operations, our approach increases efficiency, reduces cost and risk, and produces better data for our clients.

Our work is a vital step in making safe, effective treatments available to people around the world. Backed by Pencarrow, one of New Zealand's most respected and experienced private equity companies, our goals for growth are exponential.

Job DescriptionOverview

Location: Takapuna, Auckland
Role: Feasibility Specialist
Hours: Full time
Description: Please see the position details below and the form at the bottom of the page to apply.

We are seeking a talented and proactive Clinical Trials Feasibility Specialist to join our team. This pivotal role is essential in positioning PCRN to win valuable clinical trials through strategic feasibility assessments and compelling presentations of our capabilities. You will be the driving force behind our efforts to secure trial opportunities, showcasing our network's strengths and ensuring we consistently put our best foot forward with sponsors and CROs to be awarded these trials.

Why This Role Matters

As our Clinical Trials Feasibility Specialist, you will be instrumental in evaluating and analysing the viability of clinical trial protocols across multiple therapeutic areas. Your comprehensive feasibility assessments will ensure successful inclusion of PCRN in trials, ultimately supporting our organisation's goal of bringing new treatments to patients.

Key Responsibilities:

Feasibility Strategy:

  1. Lead feasibility analysis activities for assigned clinical trials
  2. Gather and evaluate historical performance data, patient populations, and competitive trial landscape
  3. Develop feasibility RFPs and content to support PCRN inclusion
  4. Conduct country-specific research on regulatory requirements, Standard of Care and patient availability
  5. Work with sites to progress through the Site Selection phase and ensure documentation completion

Client Engagement:

  1. Build strong relationships with pharmaceutical sponsors and CROs to advocate for site inclusion
  2. Showcase site capabilities and performance metrics to potential sponsors
  3. Negotiate and influence sponsor decisions regarding site selection
  4. Implement strategies to increase site visibility in the clinical trials landscape
  5. Represent our organisation at industry events and sponsor meetings
  6. Track and report on the effectiveness of engagement strategies and outcomes
What we're looking for:
  1. 2+ years of experience preferably in clinical research, with focus on feasibility assessment
  2. Understanding of clinical trial processes, ICH-GCP guidelines, and regulatory requirements
  3. Bachelor's or Master's degree in Pharmacology, Life Sciences, Healthcare, or related field
  4. Excellent organisational skills with a focus on being highly responsive
  5. Strong project management abilities and multi-tasking capabilities
  6. Outstanding written and verbal communication skills
  7. Detail-oriented approach with strong problem-solving capabilities
  8. Strategic relationship building capabilities
  9. Commercial awareness of the clinical trials industry
  10. Excellent analytical and statistical interpretation skills
  11. Ability to work both independently and collaboratively
  12. Adaptability to changing priorities and deadlines
What we can offer:
  1. A supportive and collaborative work environment where your contributions are recognised and appreciated.
  2. The opportunity to contribute to innovative clinical research that has real world impact.
  3. The opportunity to develop your career in research while working with a great team of people who love what they do.
  4. Competitive salary and benefits.
  5. Free car parking in Takapuna
  6. Coffee machine on site
  7. New purpose-built site

If you're ready to lead exciting research initiatives and be part of a forward-thinking company dedicated to improving lives, we'd love to hear from you.

Please provide answers to the following questions in your application:

  1. Please describe your right to work in New Zealand.
  2. How much notice are you required to give your current employer?
  3. How many years' experience do you have?
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