* Contribute to the development of innovative cancer therapies by working collaboratively with R&D, program management, clinical operations, biostatistics, and data management teams
* Contribute to the clinical strategy and development plans for various oncology indications
* Provide scientific input to preclinical pharmacology studies
Client Details
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Privately funded Global Biopharmaceutical company with a global presence and plans for launching an IPO in the near term.
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Our client's mission is to improve the lives of cancer patients worldwide by developing safe and effective treatment options.
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Utilising pioneering cutting-edge cancer therapies to treat cancer at the tumour site, their approved technology offers a minimally invasive and targeted alternative to surgery.
Description
* Join our clients team as a Clinical Scientist and be a key player in the development of innovative cancer therapies that have the potential to transform patients' lives worldwide. As a Clinical Scientist, you will work collaboratively with our R&D, program management, clinical operations, biostatistics, and data management teams to provide scientific support for clinical development activities.
* You will have the opportunity to contribute to the clinical strategy and development plans for various oncology indications, provide scientific input to preclinical pharmacology studies, and collaborate on the review, analysis, and interpretation of study results. You will also prepare data and contribute to scientific publications and support the development of program documents to aid in product approvals.
* In this role, you will have the chance to develop and cultivate relationships with external partners, including clinical investigators, clinicians, scientists, and vendors. Additionally, you will participate in advisory boards, consultant meetings, and investigator meetings, providing valuable insights and delivering impactful presentations.
* Our client is looking for a candidate with a working knowledge of drug development processes, GCP, ICH guidelines, and PMDA / FDA regulations. Proactive and able to anticipate potential study problems, you will also seek out and recommend process improvements.
* In the interest of improving cancer patients lives, our client is committed to providing effective and safe treatment while minimising side effects.
Profile
* Native level Japanese
* Fluent English (spoken and written)
* Extensive experience in clinical development strategy
* Experience in planning and execution of oncology clinical studies
Job Offer
* Challenging career development opportunities in a growing biotech company
* Commit to developing life changing and groundbreaking therapies that will help cancer patients globally
* Be part of a truly global organisation, with opportunities to contribute to strategic design and implementation of for Japan, US and APAC studies
Page Group Japan is acting as an Employment Agency in relation to this vacancy.

Clinical Science Lead - Biotech

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