My client is a globally recognized biotechnology company at the forefront of pioneering research. My client is seeking seeking an individual with a healthy blend of scientific expertise, clinical development experience, and a comprehensive understanding of regulatory requirements, with experience in Genetic Obesity research.
Role Overview: As a Genetic Obesity SME, this consultant will play a crucial role in conducting a deep dive into the scientific landscape of genetic obesity. These insights will drive research and clinical development strategies in this innovative field.
Key Responsibilities:
- Perform a detailed review of existing scientific literature and ongoing research in genetic obesity.
- Provide expert insights to guide research and clinical development strategies.
- Collaborate with internal teams, including R&D, clinical operations, and regulatory affairs, ensuring alignment of scientific understanding and strategy.
- Stay updated on emerging trends, technologies, and developments in genetic obesity research.
- Prepare and deliver detailed reports and presentations to convey findings and recommendations to diverse stakeholders.
Qualifications:
- Advanced degree (PhD preferred) in Genetics, Molecular Biology, or a similar field.
- Minimum 5 years of experience in pharmaceutical sponsor research, with some experience in obesity and related genetic disorders.
- Demonstrated experience in genetic obesity research, with record of publications.
- Experience in clinical development, including the design and implementation of clinical trials.
- Understanding and familarity with the regulatory environment and requirements in the pharmaceutical industry.
- Exceptional communication and presentation skills, capable to convey complex scientific concepts effectively.
- Strong analytical and problem-solving skills, paired with a commitment to scientific rigor and detail.
- Ability to work independently and collaboratively within a team.
