Senior Clinical Scientist & Study Leader

Socket.dev; United States; Remote; USD 171,000 - 236,000; Full time

Benefits offered by this job

Competitive salary and annual bonus

Comprehensive benefits package

Generous parental leave and growth机会

Company culture and professional开发

Job summary

Deciphera is seeking an Associate Director Clinical Scientist to contribute to the clinical development plan for candidate drug products, coordinating with project leaders and medical directors.

You will monitor data in real time, review regulatory documents, and perform data analyses for data cleaning and interpretation, collaborating across clinical operations, biostatistics, regulatory, and medical affairs in a multidisciplinary environment.

Qualifications

• PhD or equivalent plus 5+ years in pharmaceutical clinical development.
• Strong organizational skills to ensure data collection and documentation for analyses.
• Ability to interact with internal teams and external partners effectively.
• Experience with clinical data analysis and regulatory processes.
• Ability to influence decision-making within a multidisciplinary team.
• Excellent communication and presentation skills.

Responsibilities

• Monitor clinical data quality and patient safety on an ongoing basis.
• Collaborate with data management, clinical operations, and medical monitors.
• Author and review clinical study documents and regulatory submissions.
• Prepare and present study data to internal/external stakeholders.
• Coordinate study team meetings and site communications.

Skills

Clinical data analysis

Regulatory/document review

Cross-functional collaboration

Effective communication

Education

PhD or equivalent

Bachelor's or Master's + 10+ years experience

Tools

EDC systems

Regulatory submission tools

Job description

Deciphera is seeking an Associate Director Clinical Scientist to contribute to the clinical development plan for candidate drug products, coordinating with project leaders and medical directors.

You will monitor data in real time, review regulatory documents, and perform data analyses for data cleaning and interpretation, collaborating across clinical operations, biostatistics, regulatory, and medical affairs in a multidisciplinary environment.