Senior Manager, Clinical Scientist, Dermatology
Kymera Therapeutics
1 month ago
Remote friendly (Greater Boston)
United States
Clinical Research and Development
How you’ll make an impact:
- Contribute to the execution of clinical trial protocols in Dermatology/Immunology, working closely with the Clinical Science Study Lead to support high-quality, scientifically rigorous study conduct.
- Support day-to-day study activities with Clinical Operations, ensuring alignment with scientific, organizational, and regulatory standards.
- Conduct ongoing clinical data review and cleaning to ensure data quality, integrity, and patient safety.
- Perform medical data monitoring, including review of safety data, listings, and outputs; partner with Data Management and Medical Development for escalation, query generation, and resolution.
- Identify, analyze, and interpret clinical data trends; communicate findings and escalate to the Clinical Science Study Lead as appropriate.
- Contribute to the development and review of study-related documents (e.g., protocols, amendments, clinical study reports).
- Support interactions with investigators, CROs, and vendors during study conduct.
- Collaborate in a matrix environment with medical directors, regulatory affairs, translational medicine, clinical operations, data management, biostatistics, and other departments to drive clinical development programs forward.
Skills and experience you’ll bring:
- Bachelor’s or advanced degree (MSc, PharmD, MD, PhD) in Life Sciences or related field.
- 2+ years in pharmaceutical clinical drug development, with experience in global clinical trials and program execution.
- Experience in immunological diseases (e.g., Atopic Dermatitis) and understanding of disease biology and treatment landscapes (plus).
- In-depth understanding of clinical development processes, regulatory requirements, and guidelines (FDA, EMEA, ICH, GCP).
- Strong critical-thinking and problem-solving abilities; excellent medical writing skills.
Compensation:
- Anticipated base salary range: $145,000–$215,000; eligibility for annual bonus, equity participation, and comprehensive benefits.
- Contribute to the execution of clinical trial protocols in Dermatology/Immunology, working closely with the Clinical Science Study Lead to support high-quality, scientifically rigorous study conduct.
- Support day-to-day study activities with Clinical Operations, ensuring alignment with scientific, organizational, and regulatory standards.
- Conduct ongoing clinical data review and cleaning to ensure data quality, integrity, and patient safety.
- Perform medical data monitoring, including review of safety data, listings, and outputs; partner with Data Management and Medical Development for escalation, query generation, and resolution.
- Identify, analyze, and interpret clinical data trends; communicate findings and escalate to the Clinical Science Study Lead as appropriate.
- Contribute to the development and review of study-related documents (e.g., protocols, amendments, clinical study reports).
- Support interactions with investigators, CROs, and vendors during study conduct.
- Collaborate in a matrix environment with medical directors, regulatory affairs, translational medicine, clinical operations, data management, biostatistics, and other departments to drive clinical development programs forward.
Skills and experience you’ll bring:
- Bachelor’s or advanced degree (MSc, PharmD, MD, PhD) in Life Sciences or related field.
- 2+ years in pharmaceutical clinical drug development, with experience in global clinical trials and program execution.
- Experience in immunological diseases (e.g., Atopic Dermatitis) and understanding of disease biology and treatment landscapes (plus).
- In-depth understanding of clinical development processes, regulatory requirements, and guidelines (FDA, EMEA, ICH, GCP).
- Strong critical-thinking and problem-solving abilities; excellent medical writing skills.
Compensation:
- Anticipated base salary range: $145,000–$215,000; eligibility for annual bonus, equity participation, and comprehensive benefits.