SystImmune
Overview
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the companys success.
Responsibilities
Monitor, review, and summarize safety and efficacy data in 1 or more ongoing studies on a regular basis
Work in close collaboration with the clinical team to ensure translation of the clinical protocol (and amendments) into operational deliverables, including but not limited to performing ongoing review and analysis of clinical study data and preparing/reviewing study plans (i.e., Medical Monitoring, Medical Data Review, Safety Management, CRF Completion Guidelines, etc.)
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 and summarize the relevant scientific, drug development, and medical literature to support new clinical trial design as well as the development of clinical and/or regulatory documents
Support preparation of scientific material
Contribute to the development of SOPs and associated 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 requirement: at least 3-4 years’ industry experience (clinical research preferred)
Therapeutic areas of expertise must include oncology
Experience with data cleaning, visualization, and basic statistical analysis (Excel mandatory, R optional)
Knowledge of the International Council of Harmonization (ICH), GCP, and other relevant regulatory guidelines
Ability to analyze, interpret and socialize data to internal and external stakeholders
Strong communication, presentation, analytic, and strategic capabilities and ability to effectively collaborate with medical experts
Ability to think strategically and creatively, function independently, deliver on timelines, and contribute strategic insights
Compensation and Benefits The expected base salary range for this position is $80,000 to $130,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidates qualifications, experience, and skills. While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise align strongly with the requirements of the role.
SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the companys success. SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
Were committed to equal opportunity in all aspects of employment and do not discriminate on the basis of race, color, religion, sex, national origin, age, disability, veteran status, or any other protected characteristic.
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Responsibilities
Monitor, review, and summarize safety and efficacy data in 1 or more ongoing studies on a regular basis
Work in close collaboration with the clinical team to ensure translation of the clinical protocol (and amendments) into operational deliverables, including but not limited to performing ongoing review and analysis of clinical study data and preparing/reviewing study plans (i.e., Medical Monitoring, Medical Data Review, Safety Management, CRF Completion Guidelines, etc.)
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 and summarize the relevant scientific, drug development, and medical literature to support new clinical trial design as well as the development of clinical and/or regulatory documents
Support preparation of scientific material
Contribute to the development of SOPs and associated 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 requirement: at least 3-4 years’ industry experience (clinical research preferred)
Therapeutic areas of expertise must include oncology
Experience with data cleaning, visualization, and basic statistical analysis (Excel mandatory, R optional)
Knowledge of the International Council of Harmonization (ICH), GCP, and other relevant regulatory guidelines
Ability to analyze, interpret and socialize data to internal and external stakeholders
Strong communication, presentation, analytic, and strategic capabilities and ability to effectively collaborate with medical experts
Ability to think strategically and creatively, function independently, deliver on timelines, and contribute strategic insights
Compensation and Benefits The expected base salary range for this position is $80,000 to $130,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidates qualifications, experience, and skills. While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise align strongly with the requirements of the role.
SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the companys success. SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
Were committed to equal opportunity in all aspects of employment and do not discriminate on the basis of race, color, religion, sex, national origin, age, disability, veteran status, or any other protected characteristic.
#J-18808-Ljbffr