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- Tasks: Lead clinical trials and develop innovative strategies to improve health outcomes.
- Company: Join AbbVie, a leader in healthcare innovation and patient impact.
- Benefits: Competitive salary, comprehensive health benefits, and opportunities for professional growth.
- Why this job: Make a real difference in patients' lives through groundbreaking medical research.
- Qualifications: Medical degree with experience in clinical development and strong communication skills.
- Other info: Collaborative environment focused on integrity, innovation, and community service.
The predicted salary is between 54000 - 84000 £ per year.
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
Supports the TA Head and Global TA Science Lead, proposes development strategies and clinical pathways for new compound registrations in China. Acts as China Local Clinical Leader to lead evidence generation working group for excellent delivery for trials in China and to assess new trial opportunities. Provides scientific expertise in prioritizing diseases and compounds for China, including opportunities for alliances and partnerships. Provides China scientific inputs to the global TPP.
Provides China clinical expertise to design clinical development plans and protocol discussion, ensuring the study design meets the local regulatory requirements, aiming for efficient development tactics for registration. Initiates proper Development-led medical activities, i.e. medical surveys, Ad Board meetings, KOL visits and other insights development, to support clinical development plan formation and execution.
Works closely with Regulatory Affairs to develop an efficient pathway for registration with scientific justification, generating and reviewing China regulatory filing materials, based on clinical expertise from CTA through NDA approval. Establishes scientific partnership with Chinese academia and key study centers for effective planning and high-quality implementation in China.
Provides medical/scientific training on program specific standards to CDO and investigators to ensure consistency through the process of design, conduct and reporting of clinical trials. Provides local medical support to Global study team, including trial medical monitoring, responding to protocol-specific site questions, resolving data queries, and performing analysis to address questions on efficacy and safety etc.
Ensures seamless communication and handover to medical affairs of approved indications and support launch activities. Ensures all activities are in compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie's policies, procedures and accepted standards of best practice.
Qualifications
IDEAL CANDIDATE: Medical Degree or Bachelor's degree. With strong medical background and clinical practice experience of related TA area (psychiatry or neurology), adequate knowledge of the drug development process and the regulatory framework for clinical development. Working experiences (> 4 years) in medical and clinical development group of pharmaceutical (or biopharmaceutical) company or equivalent clinical practice is essential.
Clear understanding of the developmental program interplay among Regulatory Affairs, Clinical Development and Commercial objectives. Experienced in leading multiple, diverse clinical development programs is a plus. Strong insights to study design, good knowledge of data collection, management, analysis, and interpretation are required.
Strong verbal and written communication skills are required to complement the ability to analyze and summarize scientific/clinical data, and develop recommendations that affect the conduct of trial and the content of regulatory documents. Effective collaboration with peers, stakeholders and partners to achieve positive impact to development results. High customer orientation and patient-centric thinking. Strong commitment to be compliant with all the relevant rules and procedures, and to scientific quality and integrity. Fluent spoken English and solid written English skills.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.
Senior Clinical Research Physician employer: AbbVie
Contact Detail:
AbbVie Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Physician
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. We can leverage our connections to get insights and even referrals that could land us an interview.
✨Tip Number 2
Prepare for those interviews! Research AbbVie’s recent projects and therapeutic areas they focus on. We should be ready to discuss how our experience aligns with their mission and how we can contribute to their innovative solutions.
✨Tip Number 3
Showcase our expertise! During interviews, we can share specific examples of our past work in clinical development and how it relates to the role. Let’s make sure to highlight our understanding of regulatory frameworks and study design.
✨Tip Number 4
Don’t forget to follow up! After an interview, we should send a thank-you email expressing our appreciation for the opportunity. It’s a great way to reinforce our interest in the position and keep us top of mind.
We think you need these skills to ace Senior Clinical Research Physician
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that align with the Senior Clinical Research Physician role. Highlight your medical background, clinical practice experience, and any relevant projects you've led.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about AbbVie's mission and how your expertise can contribute to their innovative solutions in health care.
Showcase Your Communication Skills: Since strong verbal and written communication skills are key for this role, ensure your application materials are clear, concise, and free of jargon. This will demonstrate your ability to analyse and summarise complex data effectively.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets the attention it deserves and allows us to keep track of all applicants efficiently.
How to prepare for a job interview at AbbVie
✨Know Your Stuff
Make sure you brush up on the latest developments in immunology, oncology, neuroscience, and eye care. AbbVie is all about innovative medicines, so being able to discuss recent advancements or clinical trials in these areas will show your passion and expertise.
✨Understand the Regulatory Landscape
Familiarise yourself with the regulatory framework for clinical development, especially in China. Knowing how the drug development process works and being able to discuss it confidently will demonstrate your readiness for the role.
✨Showcase Your Collaboration Skills
Prepare examples of how you've effectively collaborated with peers and stakeholders in previous roles. AbbVie values teamwork, so highlighting your ability to work well with others will be a big plus.
✨Communicate Clearly
Practice articulating complex scientific concepts in a clear and concise manner. Strong verbal and written communication skills are essential, so consider doing mock interviews to refine your delivery and ensure you can summarise data effectively.
