SystImmune Inc.
Medical Director/Senior Director, Clinical Research
SystImmune Inc., Redmond, Washington, United States, 98052
Medical Director/Senior Director, Clinical Research
Redmond, WA
Located in Redmond WA, SystImmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic bi-specific, and tri-specific antibodies, as well as antibody-drug conjugates (ADC's). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. Job Summary:
Oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Key Responsibilities:
Manages the design and implementation of one or more clinical development programs based on strong medical and scientific principles, knowledge of compliance and regulatory requirements. Oversees project-related education of investigators, study site personnel and internal study staff. Has overall responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the compound. Responsible for design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other study/program documents. Responsible, with limited supervision, for the proactive monitoring of clinical trial safety which is conducted in collaboration with the Safety team. May oversee the work of other Medical Director(s) and of Clinical Scientists working on the same or related study/programs. Provides in-house clinical expertise for compound(s) and indications, coordinating appropriate scientific and medical activities with internal stakeholders as they relate to ongoing clinical study/projects. Serves as the medical representative/lead in Clinical Study Team (CST), with responsibility for development of a rigorous, cross-functionally-aligned medical oversight. Acts as a clinical interface and actively solicits opinion leader interactions related to the compound and disease area. Stays abreast of professional information and technology through conferences, medical literature, and other available training. Responsible for understanding the regulatory requirements related to clinical studies and global drug development and accountable for complying with those requirements. Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. Required Skills & Qualifications
M.D. or equivalent in ex-US countries. A minimum of 2 years for Director level and 4 years for Sr Director level of experience in medical monitoring of Oncology clinical trials is required. Track record of successful management of product safety in phase 1 and/or 2 Oncology clinical trials. Experience in the clinical and drug development process in a global pharmaceutical/biotechnology company. Advanced analytical skills. Basic leadership and decision-making skills. Advanced communication skills. Sound medical judgment and experience in medical safety interpretation of safety findings for clinical trials. Basic clinical and/or drug development expertise. Good organizational and prioritization skills. Intermediate skill in strategic thinking and planning activities. Basic negotiation skills and capabilities to influence. Good interpersonal skills (i.e. team player). Intermediate computer skills (MS Office); knowledge of most common EDC systems, ARGUS, JReview is a plus. Working knowledge of MedDRA. Basic statistics and Pharmacoepidemiology. Ability to work with limited supervision. Ability to establish sound working relationships with people globally. Flexibility and ability to adapt and learn quickly. Ability to work under pressure and to tight deadlines. Must possess excellent oral and written English communication skills. Willing to travel 20-30% of time. The hiring pay range for this position is $210,000 - $280,000 per year based on skills, education, and experience relevant to the role. SystImmune is a stable, well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. 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 an Equal Opportunity Employer. Interested applicants should send their CV and cover letter to hr@systimmune.com
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Redmond, WA
Located in Redmond WA, SystImmune Inc. is a bio-pharmaceutical company focused on the treatment of cancer through developing novel therapeutic bi-specific, and tri-specific antibodies, as well as antibody-drug conjugates (ADC's). Our objective is to create biologics that work through systematic intervention on the solid tumor micro-environment, to either directly attack the tumor and/or to activate the immune system to attack the tumor. Job Summary:
Oversees the direction, planning, execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business strategy. Key Responsibilities:
Manages the design and implementation of one or more clinical development programs based on strong medical and scientific principles, knowledge of compliance and regulatory requirements. Oversees project-related education of investigators, study site personnel and internal study staff. Has overall responsibility for oversight of clinical studies, monitoring overall study integrity and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the compound. Responsible for design, analysis, interpretation and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and other study/program documents. Responsible, with limited supervision, for the proactive monitoring of clinical trial safety which is conducted in collaboration with the Safety team. May oversee the work of other Medical Director(s) and of Clinical Scientists working on the same or related study/programs. Provides in-house clinical expertise for compound(s) and indications, coordinating appropriate scientific and medical activities with internal stakeholders as they relate to ongoing clinical study/projects. Serves as the medical representative/lead in Clinical Study Team (CST), with responsibility for development of a rigorous, cross-functionally-aligned medical oversight. Acts as a clinical interface and actively solicits opinion leader interactions related to the compound and disease area. Stays abreast of professional information and technology through conferences, medical literature, and other available training. Responsible for understanding the regulatory requirements related to clinical studies and global drug development and accountable for complying with those requirements. Ensures adherence to Good Clinical Practices, pharmacovigilance standards, standard operating procedures and to all other quality standards in conducting research. Required Skills & Qualifications
M.D. or equivalent in ex-US countries. A minimum of 2 years for Director level and 4 years for Sr Director level of experience in medical monitoring of Oncology clinical trials is required. Track record of successful management of product safety in phase 1 and/or 2 Oncology clinical trials. Experience in the clinical and drug development process in a global pharmaceutical/biotechnology company. Advanced analytical skills. Basic leadership and decision-making skills. Advanced communication skills. Sound medical judgment and experience in medical safety interpretation of safety findings for clinical trials. Basic clinical and/or drug development expertise. Good organizational and prioritization skills. Intermediate skill in strategic thinking and planning activities. Basic negotiation skills and capabilities to influence. Good interpersonal skills (i.e. team player). Intermediate computer skills (MS Office); knowledge of most common EDC systems, ARGUS, JReview is a plus. Working knowledge of MedDRA. Basic statistics and Pharmacoepidemiology. Ability to work with limited supervision. Ability to establish sound working relationships with people globally. Flexibility and ability to adapt and learn quickly. Ability to work under pressure and to tight deadlines. Must possess excellent oral and written English communication skills. Willing to travel 20-30% of time. The hiring pay range for this position is $210,000 - $280,000 per year based on skills, education, and experience relevant to the role. SystImmune is a stable, well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. 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 an Equal Opportunity Employer. Interested applicants should send their CV and cover letter to hr@systimmune.com
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