位于外滩的 20 个优质data scientist职位（正在招聘！）

Participate in the design and execution of clinical trials of their assigned programs, helping to create the clinical development plan for new compounds, and pave a path towards regulatory approval.
Works hand-in-hand with the (Senior) Director Clinical Development to drive clinical strategies and their operationalization in programs and trials.

Collaborative with other functions in operational planning, content, execution and delivery for assigned programs and studies. Will manage day-to-day clinical activities for our clinical studies including management of protocol amendments, overseeing data review activities, conducting medical data review and communicating with investigator / sites where appropriate.

Assumes Trial Lead responsibilities in the assigned programs, in liaison with the responsible program manager. Collaborate with the program core team.
Contribute to create and translate Target Product Profile into clinical strategy.
As Trial Lead, articulates targets of TPP and CDP to other development functions (e.g. Regulatory, Pharmacovigilance, Statistics, etc.) and drives alignment on objectives and expected outcomes. Helps translate Target Product Profile into clinical strategy.
Collaborates closely with Pharmacovigilance on development of Risk Management Plans.

Collaborates and gives guidance for the Clinical Trial Scientists, and works with them on day-to-day basis on clinical trials, driving overall progress of study implementation.
Responsible for developing data review strategy and conducting ongoing medical monitoring activities including medical data review.

Support preparation and participate in study level meetings, for example investigator meetings, data monitoring meetings, and others.Ensures at the program and trial level, that the clinical development team works hand-in-hand with Clinical Operations team, with a focus on patient centric drug development, ensuring balancing of high medical quality, trial complexity, as well as time and cost considerations.
Takes ownership together with partner functions in Development on the acceleration of program, trial design, and innovation for the patient (e.g. digital endpoints, synthetic control arms, RWE/ HEOR, PRO, Medical Affairs)
Creates input for clinical sections of key documents, including Investigator's Brochures, IND summary documents, CTAs, responses to questions from regulatory authorities, IRBs and ethics committees, and NDAs.

Creates Clinical Study Report (CSR) medical content and ensures it meets high quality expectations on medical standards, provides respective guidance to other members of the clinical development team

Establishes and manages relationships with key external stakeholders (industry partners, Key Opinion Leaders, health authorities).
Participant decision/governance meetings, senior management, or advisory boards as applicable.

Contributes to a collaborate culture within and outside Clinical Development and actively share best practice within the clinical team.

What you have to offer:

Master degree with strong scientific and clinical background in Immuno-Oncology, Oncology
Minimum of 3 years of experience within Immuno-Oncology, Oncology at the biotech/pharmaceutical and the academic setting, including leading clinical development programs from exploratory Phase I/II clinical studies through late stage development in Phase III and regulatory submissions. Total 5 years’ experience in related area.
Good understanding of the clinical and scientific methods and approaches used in clinical development studies, as novel clinical study designs, application of companion diagnostics for patient selection, clinical pharmacology/ translational modeling and biostatistics. Complemented with several years of experience on confirmatory PH3 trial design and respective dossier preparation and submission activities.
Experienced in global health authority interactions (EMA, FDA, MHRA, CDE). Having participated or led a drug development program to successful registration is an advantage.
Strong medical experience in medical monitoring including overseeing and interpreting safety and efficacy clinical trial data and ensuring appropriate contact for study medical and patient safety aspects.
Ability to strategize clinical activities based on a TPP and CDP and translate into trial designs
Ability to write high quality and executable trial designs and protocols
High level of comfort and demonstrated successes working in a matrix environment (global and cross-functional), including contributing to establishing clarity and structures and driving state of the art collaborations with external academic and industry partners.
A genuine interest and understanding of the science supporting the clinical development programs. Confident to discuss and present scientific and mechanistic aspects of drug development.

Subject matter expertise on drug development topics, and genuine interest to drive innovation and continuous improvement

High proficiency in English (written and spoken)

Apply now - We look forward to receiving your application!

Apply to our Shanghai, China location by sending us your documents via our online form. For any questions, contact our talent acquisition team on: + 49 (0) 6131-9084-1291 (Monday-Friday from 1 PM to 3 PM CET).

Job ID 9282 (please always specify if you have any questions)

By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.

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BioNTech, the story

At BioNTech, we are more than just a biotechnology company – we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.

Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.

Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.

BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!

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