The Clinical Scientist plays a key role in the execution and operational support of clinical trials, assisting in the collection and review of clinical data to ensure study success.
This role involves supporting protocol development, study implementation, data review, and documentation preparation to align with clinical development goals.
The Clinical Scientist collaborates closely with cross-functional teams to ensure the generation of high-quality clinical data.
Additionally, they work closely with the Medical Director, Clinical Development to execute key tasks.
Contributes to the development of clinical trial protocols, including patient selection criteria, study endpoints, and data collection methods.
Monitors the data of clinical trials at study sites, ensuring adherence to protocols and good clinical practice (GCP) guidelines.
Perform data review, reconciliation and standardization to ensure high quality outputs.
Reviews clinical data to support in the assessment of the safety and efficacy of the investigational drug.
Supports the development of clinical documents required during the clinical development process.

Advanced degree in life sciences, such as a PhD, PharmD or related field
Understanding of clinical trial methodologies and regulatory requirements
Experience in clinical study design, data analysis, data review and interpretation
Good written and verbal communication skills
Ability to work effectively in a collaborative, cross-functional environment
3 years experience

A chance to be part of a vibrant startup culture where your work can directly impact bringing new medicines to patients.
Competitive salary and benefits package.
A supportive and inclusive team environment where everyone is encouraged to bring their authentic selves to work.
Opportunities for professional growth and development.

Clinical Scientist, Clinical Development

Key skills