This range is provided by Clinical Dynamix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
$175,000.00/yr - $200,000.00/yr
Associate Director, Clinical Scientist
How you’ll make an impact:
* Serve as the study lead Clinical Scientist in immunology, actively participating in program team meetings, scientific advisory boards, and data/safety monitoring committees.
* Support the design of clinical trial protocols, synopses, and amendments, ensuring scientific integrity and alignment with regulatory standards.
* Conduct clinical and medical data reviews, including safety monitoring activities, to ensure patient safety and data accuracy.
* Collaborate with Translational Medicine to embed bioanalytical sampling (e.g., PK/PD, biomarker assays) into trial protocols; ensure data flow to functional groups for analysis.
* Prepare and review essential documents such as medical monitoring plans, statistical analysis plans (SAPs), informed consent forms, and clinical study reports, supporting regulatory submissions.
* Work within a matrix environment, collaborating with medical directors, regulatory affairs, translational medicine, clinical operations, statistics, and other departments to drive clinical development programs forward.
* Review monitoring reports, track protocol deviations, monitor data, query resolution, analyze trends, and prepare clinical study reports and regulatory submission materials.
* Present data and information to external investigators and internal stakeholders, contributing to meetings with governance bodies and regulatory authorities.
Skills and experience you’ll bring:
* Bachelor’s or advanced degree (MSc, PharmD, MD, PhD) in Life Sciences, Pharmacology, or related field.
* 4+ years in pharmaceutical clinical drug development, with experience in global clinical trials and program execution.
* Proficiency in immunological diseases (e.g. Atopic dermatitis, Asthma) including an understanding of disease biology and treatment landscapes.
* In-depth understanding of clinical development processes, regulatory requirements, and guidelines (FDA, EMEA, ICH, GCP).
* Strong problem-solving abilities and excellent medical writing skills.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Science and Research
* Industries
Pharmaceutical Manufacturing and Biotechnology Research
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