Associate Director or Director, Clinical Scientist

Scorpion Therapeutics; United States; On-site; USD 140,000 - 230,000; Full time

Job summary

Kymera Therapeutics seeks a Clinical Scientist focused on immunology with dermatologic indications. You will design and support clinical trial protocols, ensure scientific and regulatory compliance, and prepare critical documentation.

You will contribute to trial execution, safety monitoring, data reviews, and risk mitigation while supporting regulatory submissions and interactions with investigators and internal stakeholders.

Qualifications

• 8+ years of experience in global pharmaceutical clinical trials and program management.
• Experience in immunology with a focus on dermatologic diseases.
• Deep understanding of clinical development processes, regulatory standards (FDA, EMEA, ICH, GCP).

Responsibilities

• Design and support clinical trial protocols.
• Ensure scientific and regulatory compliance.
• Prepare key trial documentation.
• Contribute to trial execution and safety monitoring.
• Engage in data reviews, trend analysis and risk mitigation.
• Support regulatory submissions and interactions with investigators and internal stakeholders.

Skills

Immunology experience

Dermatology focus

Clinical trial design

Regulatory knowledge

Education

Bachelor's or higher in Life Sciences

MSc in Life Sciences

PharmD/PhD in Life Sciences

Job description

Role: Serve as a Clinical Scientist focused on immunology, particularly dermatologic indications, within Kymera's clinical development team. Responsibilities include designing and supporting clinical trial protocols, ensuring scientific and regulatory compliance, preparing key documentation, and contributing to trial execution and safety monitoring. Engage in data reviews, trend analysis, and risk mitigation, while supporting regulatory submissions and interactions with external investigators and internal stakeholders. Work collaboratively across functions such as Translational Medicine, Clinical Pharmacology, Medical, Regulatory, Data Management, and Biostatistics.

Qualifications: Bachelor's or higher degree (MSc, PharmD, PhD) in Life Sciences or related field, with 8+ years of experience in global pharmaceutical clinical trials and program management. Experience in immunology, with a focus on dermatologic diseases, and familiarity with clinical endpoints and disease biology is preferred. Deep understanding of clinical development processes, regulatory standards (FDA, EMEA, ICH, GCP), and patient-centric approaches are required.

High-Value: Immunology, dermatology, clinical trial design, pharmacokinetics integration, biomarker collaboration, regulatory submissions.

Work Setup: Not specified; role likely involves cross-functional collaboration.