- Involve in early product launch cycle|Abundant oncology pipeline
About Our Client
Our client is a global, research-driven biopharmaceutical company committed to developing innovative therapies that address some of the most challenging diseases in areas such as oncology, immunology, and neuroscience. With a focus on advancing precision medicine and biologic treatments, the organization is dedicated to improving patient outcomes and meeting unmet medical needs through a robust pipeline and strategic partnerships. By fostering a culture of collaboration, scientific excellence, and integrity, our client provides a dynamic environment where professionals can contribute to groundbreaking medical advancements while continuing to grow and develop their careers.
Job Description
- Serve as the main point of contact for thought leaders and external experts, supporting investigator-initiated studies (IIS) and fostering partnerships with key academic and research institutions.
- Collaborate with Clinical Site Management (CSM) teams to initiate, monitor, and execute clinical trials, providing scientific expertise to investigators and ensuring adherence to timelines and quality standards.
- Work with healthcare professionals to identify appropriate patient populations, provide expert guidance on clinical practices, and deliver educational presentations on the client's pipeline and disease areas.
- Gather and communicate insights from investigators and clinical sites, identify challenges, and collaborate with R&D teams to enhance clinical trial design and future development efforts.
- Ensure regulatory compliance with local and global guidelines, attend scientific meetings to stay current with industry developments, and support compassionate use requests where applicable.
The Successful Applicant
- PhD, MD, and PharmD in a relevant scientific discipline is preferred. Candidates with a graduate degree and proven experience in the field will also be considered.
- Minimum of 2 years of professional experience in a field-based R&D role, such as Medical Science Liaison (MSL), CRA, or a similar function.
- Deep understanding of the pharmaceutical industry and the role of Medical Affairs in supporting clinical research and scientific objectives.
- Strong knowledge of clinical research methodologies and current regulatory and legislative controls relevant to clinical trials.
- Demonstrated ability to develop and maintain expertise in assigned therapeutic areas and translate complex scientific data into practical insights.
- Proven ability to build and maintain strong relationships with external experts, investigators, and healthcare professionals.
- High level of scientific and ethical integrity, with a strong commitment to compliance and quality in all professional activities.
- Proficiency in English (both written and spoken) is desirable.
- Strong customer orientation with an ability to address healthcare professionals needs and contribute to clinical development objectives.
- Ability to work independently and manage multiple priorities in a dynamic, fast-paced environment.
- Team player with strong interpersonal and networking skills.
- A high level of initiative, problem-solving capabilities, and attention to detail.
What's on Offer
The opportunity to engage with and contribute to
our client's state-of-the-art oncology pipeline offers you a chance to be at the forefront of developing groundbreaking therapies. You'll work on therapies that could transform cancer treatment and improve patient outcomes globally.
Contact: Jenny I Wang
Quote job ref: JN-112024-6587241
