Systimmune
Manager, Clinical Science
SystImmune is a leading, well‑funded clinical‑stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. We specialize in developing innovative cancer treatments using bi‑specific, multi‑specific antibodies and antibody‑drug conjugates (ADCs). Our pipeline includes multiple assets in various stages of clinical trials for solid tumor and hematologic indications, as well as a robust preclinical portfolio in the discovery and IND‑enabling stages. We are seeking a motivated Manager, Clinical Science to join our clinical development team and contribute to the advancement of innovative therapeutic programs. This role provides an excellent opportunity to gain hands‑on experience in clinical trial design and execution while working alongside experienced clinical development professionals in a dynamic biotech/pharmaceutical environment. Responsibilities
Monitor, review, and summarize safety and efficacy data in ongoing studies on a regular basis. Work closely with the clinical team to translate the clinical protocol (and amendments) into operational deliverables, including review and analysis of clinical study data and preparation/review of study plans. Respond to study questions from sites and/or vendors, with study medical monitor or Clinical Development supervision where needed. Perform literature search and critically review relevant scientific, drug development, and medical literature to support new clinical trial design and development of clinical and/or regulatory documents. Support preparation of scientific material and contribute to development of SOPs, guidelines, and templates. Participate in cross‑functional team meetings with members from clinical operations, safety, regulatory, biostatistics, and data management. Qualifications
Degree in life sciences or health‑related field. Minimum 3–4 years of industry experience (clinical research preferred). Therapeutic area expertise must include oncology. Experience with data cleaning, visualization, and basic statistical analysis (Excel mandatory, R optional). Knowledge of ICH, GCP, and other relevant regulatory guidelines. Strong communication, presentation, analytic, and strategic capabilities with ability to collaborate effectively with medical experts. Strong strategic thinking, independence, and ability to deliver on timelines. Compensation and Benefits
Expected base salary range: $80,000 – $130,000 annually. Actual compensation will be based on a variety of factors, including qualifications, experience, and skills. SystImmune offers a comprehensive benefits package including 100% paid employee premiums for medical/dental/vision, STD, LTD, a 401(k) plan with a 50% company match up to 3%, 15 PTO days per year, sick leave, 11 paid holidays, and more. SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
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SystImmune is a leading, well‑funded clinical‑stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. We specialize in developing innovative cancer treatments using bi‑specific, multi‑specific antibodies and antibody‑drug conjugates (ADCs). Our pipeline includes multiple assets in various stages of clinical trials for solid tumor and hematologic indications, as well as a robust preclinical portfolio in the discovery and IND‑enabling stages. We are seeking a motivated Manager, Clinical Science to join our clinical development team and contribute to the advancement of innovative therapeutic programs. This role provides an excellent opportunity to gain hands‑on experience in clinical trial design and execution while working alongside experienced clinical development professionals in a dynamic biotech/pharmaceutical environment. Responsibilities
Monitor, review, and summarize safety and efficacy data in ongoing studies on a regular basis. Work closely with the clinical team to translate the clinical protocol (and amendments) into operational deliverables, including review and analysis of clinical study data and preparation/review of study plans. Respond to study questions from sites and/or vendors, with study medical monitor or Clinical Development supervision where needed. Perform literature search and critically review relevant scientific, drug development, and medical literature to support new clinical trial design and development of clinical and/or regulatory documents. Support preparation of scientific material and contribute to development of SOPs, guidelines, and templates. Participate in cross‑functional team meetings with members from clinical operations, safety, regulatory, biostatistics, and data management. Qualifications
Degree in life sciences or health‑related field. Minimum 3–4 years of industry experience (clinical research preferred). Therapeutic area expertise must include oncology. Experience with data cleaning, visualization, and basic statistical analysis (Excel mandatory, R optional). Knowledge of ICH, GCP, and other relevant regulatory guidelines. Strong communication, presentation, analytic, and strategic capabilities with ability to collaborate effectively with medical experts. Strong strategic thinking, independence, and ability to deliver on timelines. Compensation and Benefits
Expected base salary range: $80,000 – $130,000 annually. Actual compensation will be based on a variety of factors, including qualifications, experience, and skills. SystImmune offers a comprehensive benefits package including 100% paid employee premiums for medical/dental/vision, STD, LTD, a 401(k) plan with a 50% company match up to 3%, 15 PTO days per year, sick leave, 11 paid holidays, and more. SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
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