Clinical Data Scientist - Drug Development & Trials

Neurocrine Biosciences; San Diego (CA); On-site; USD 48,000 - 65,000; Full time

Benefits offered by this job

Retirement plan with company match

Paid vacation

Health benefits

Equity-based long-term incentive

Job summary

Neurocrine Biosciences is seeking a data-focused clinical professional to support clinical development in early and late phases, including study design, data analyses, and communication of results. You will contribute to multidisciplinary teams and help inform program decisions with statistical and regulatory insights.

Responsibilities include monitoring data, ensuring data integrity at sites, and drafting regulatory and clinical documents.

Qualifications

• BA/BS or MA in Data Sciences, Psychology or related field and 2+ years of industry relevant experience.
• Excellent communications, problem-solving, analytical thinking skills.
• Excellent project management skills.

Responsibilities

• Provides clinical support and scientific opinion to study teams and functional areas such as regulatory, clinical operations and line management.
• Provides input to study design, protocol concepts/protocols preparation, statistical analysis plans, and reporting within assigned programs to yield high value clinical endpoint insight for future critical decisions.
• Contributes within clinical development program teams on selection of established and development of novel outcome measures in the context of clinical trials in early and late stages of clinical development.
• Collaborates with external opinion leaders, internal clinicians, translational sciences and clinical operations to ensure appropriate study designs are achieved for successful implementation of
• Monitors patient data and study-related information related to clinical study sites and clinical trial participation.

Education

BA/BS or MA in Data Sciences, Psychology or related field

Job description

Neurocrine Biosciences is seeking a data-focused clinical professional to support clinical development in early and late phases, including study design, data analyses, and communication of results. You will contribute to multidisciplinary teams and help inform program decisions with statistical and regulatory insights.

Responsibilities include monitoring data, ensuring data integrity at sites, and drafting regulatory and clinical documents.