Consulting- Data & AI Consultant-Life Science R&D Full-time

Overview

– Serves as a bridge between scientific research and clinical practice. This role requires a deep understanding of both medical science and the research and development (R&D) process.

– Works closely with scientists, clinicians, and regulatory affairs professionals to ensure that research projects align with clinical needs and regulatory requirements

Responsibilities:

– Medical Expertise:

o Provide medical expertise and guidance to R&D projects.

o Stay up-to-date with the latest medical literature and research findings, particular in respiratory, oncology therapeutic areas.

o Evaluate the clinical relevance and potential impact of research projects.

– Regulatory Compliance:

o Ensure that research projects comply with relevant regulations and guidelines (e.g., primarily CFDA; FDA, EMA, ICH where relevant).

o Advise on regulatory strategies and submission requirements.

o Collaborate with regulatory affairs professionals to prepare and submit regulatory documents.

– Clinical Research Design:

o Advise on application of digital and data technologies in the design and execution of clinical trials.

o Leverage client’s input on study protocols, patient selection criteria, and data collection methods, to apply to data/ AI/ digital projects.

o Advise on digital methods to improve transparency of progress of clinical trials and uplift data quality.

– Scientific Communication:

o Communicate benefits of digital and data technologies to drive research findings to internal and external stakeholders, including scientists, clinicians, and regulatory bodies.

– Collaboration:

o Work closely with client experts (i.e., scientists, clinicians, and regulatory affairs professionals) to ensure effective collaboration and successful project delivery.

o Build strong relationships with client R&D stakeholders and external partners, such as academic institutions and healthcare providers.

– Medical Writing:

o Familiarity with medical writing requirements, such as clinical study reports, protocols, and regulatory submissions.

o Ensure that medical writing is clear, concise, and accurate

– MD or PhD degree in a relevant medical field.

– 5+ years of experience in medical research or clinical practice.

– 3+ years of experience in a consultancy role.

– Strong understanding of the drug development process and regulatory requirements.

– Excellent Mandarin Chinese and English communication and interpersonal skills.

– Ability to work independently and as part of a team.

– Strong medical writing skills. – Knowledge of relevant regulatory guidelines and standards

About Accenture

Accenture is a leading global professional services company that helps the world’s leading organizations build their digital core, optimize their operations, accelerate revenue growth and enhance services-creating tangible value at speed and scale. We are a talent- and innovation-led company with 774,000 people serving clients in more than 120 countries. Technology is at the core of change today, and we are one of the world’s leaders in helping drive that change, with strong ecosystem relationships. We combine our strength in technology and leadership in cloud, data and AI with unmatched industry experience, functional expertise and global delivery capability. Our broad range of services, solutions and assets across Strategy & Consulting, Technology, Operations, Industry X and Song, together with our culture of shared success and commitment to creating 360° value, enable us to help our clients reinvent and build trusted, lasting relationships. We measure our success by the 360° value we create for our clients, each other, our shareholders, partners and communities. Visit us at www.accenture.com

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