Senior Associate Director, Immunology Clinical Science

Kymera Therapeutics; Massachusetts; Sur place; USD 160 000 - 275 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Equity participation

Comprehensive benefits

Résumé du poste

Kymera Therapeutics is seeking a study level Clinical Scientist in immunology with a focus on dermatologic indications. You will participate in study team meetings, vendor meetings, and data/safety monitoring committees to drive scientific rigor in trial design and execution.

You will collaborate with Translational Medicine and Clinical Pharmacology to integrate biomarker testing and pharmacokinetic sampling into trial protocols, preparing essential documents and supporting regulatory

Qualifications

• Bachelor’s or advanced degree (MSc, PharmD, PhD) in Life Sciences or related field.
• 8+ years in pharmaceutical clinical drug development with global trials.

Responsabilités

• Serve as the study level Clinical Scientist in immunology, with a focus on dermatologic indications, participating in study team and governance meetings.
• Support design of clinical trial protocols and amendments, ensuring scientific integrity and regulatory alignment.
• Prepare medical monitoring plans, statistical analysis plans, informed consent forms, and clinical study reports.
• Support study execution as scientific subject matter expert, ensuring data quality and safety.
• Conduct clinical data reviews, including safety monitoring, to ensure patient safety and data integrity.
• Data review, cleaning, monitoring, and trend analysis to identify risks and mitigation strategies.
• Assist IRB and regulatory submissions and responses; provide data presentations to internal/external stakeholders.

Connaissances

Clinical development

Immunology

Regulatory knowledge

Medical writing

Formation

Bachelor’s or advanced degree in Life Sciences

Description du poste

Kymera Therapeutics is seeking a study level Clinical Scientist in immunology with a focus on dermatologic indications. You will participate in study team meetings, vendor meetings, and data/safety monitoring committees to drive scientific rigor in trial design and execution.

You will collaborate with Translational Medicine and Clinical Pharmacology to integrate biomarker testing and pharmacokinetic sampling into trial protocols, preparing essential documents and supporting regulatory