Are you passionate about clinical research and looking for a rewarding career in the biotech industry? Novotech, a leading global Contract Research Organization (CRO), is hiring a Feasibility Specialist in the Philippines. This is a unique opportunity to join a dynamic Business Development team, strategize clinical trial site selections, and work with global teams across the Asia-Pacific (APAC) region. Be the first to apply for this exciting role and contribute to life-changing clinical trials with a company committed to excellence, inclusivity, and innovation.
Responsibilities
As a Feasibility Specialist at Novotech, you will play a critical role in shaping clinical trial strategies. Your key responsibilities include:
- Collaborating with Client Operations Managers, Directors, and Project Managers to conduct pre-award and post-award feasibility assessments for clinical trials.
- Developing strong relationships with key opinion leaders (KOLs), investigators, and site staff across APAC to support trial success.
- Reviewing study documents (e.g., protocols, RFPs) to develop tailored feasibility strategies and country lists.
- Conducting in-depth reviews of scientific literature and commercial databases to inform feasibility reports.
- Designing study-specific feasibility questionnaires using Novotech’s CTMS Feasibility module.
- Coordinating with Country Managers and in-country teams to ensure timely and high-quality feasibility assessments.
- Analyzing responses and providing actionable insights using critical thinking and proactive follow-ups.
- Utilizing PowerBI for reporting and presenting feasibility results to clients during meetings or bid defenses.
- Preparing detailed feasibility reports for post-award studies and supporting business development handovers.
- Representing Novotech professionally at external events, acting as a brand ambassador.
Qualifications
To excel in this role, you should meet the following criteria:
- A degree in clinical or life sciences (or equivalent qualifications in allied professions).
- At least three years of experience as a Clinical Research Associate (CRA).
- Prior experience in feasibility assessments or clinical trial start-up processes is highly desirable.
- Strong communication skills, ability to prioritize tasks, and a track record of meeting tight deadlines.
- Exceptional critical thinking and attention to detail.
Benefits
Novotech is committed to being an employer of choice, offering:
- Flexible Work Options: Support for work-life balance with remote and hybrid opportunities.
- Inclusive Workplace: A culture that values diversity, including support for LGBTIQ+ individuals, people with disabilities, and those with caring responsibilities.
- Career Growth: Ongoing development programs to advance your skills in clinical research.
- Wellness Programs: Initiatives to support your physical and mental well-being.
- Paid Parental Leave: Available for both parents to ensure family-friendly policies.
How to Apply
