Clinical Scientist, Clinical Development

Key Responsibilities

• Contributes to the development of clinical trial protocols, including patient selection criteria, study endpoints, and data collection methods.
• Makes sure the data of clinical trials at study sites follows the protocols and GCP guidelines.
• Reviews clinical data to support the assessment of the safety and efficacy of the investigational drug.
• Supports the creation of clinical documents necessary during the clinical development process (such as Clinical Study Protocols, Investigator Brochures, Clinical Study Reports).

Qualifications

• 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 of experience.

Compensation

An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity. The anticipated salary range for candidates, who will work in Waltham, MA (remote may be considered) is $140,000 to $155,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc.

What We Offer

• 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.