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SciPro
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  • Head of Product (Boston)  

    - Suffolk County
    SciPro is partnered with a venture-backed TechBio company leveraging A... Read More
    SciPro is partnered with a venture-backed TechBio company leveraging AI and real-world data to transform how novel therapeutics are discovered, developed, and delivered. The company is building a scalable, data-driven platform that integrates multi-modal biological data, advanced analytics, and clinical insights to accelerate drug development and improve patient outcomes. This is a high-impact leadership opportunity to define and scale the product organization at the intersection of life sciences, AI/ML, and healthcare infrastructure within a fast-growing, deeply collaborative environment. Responsibilities Lead the overall product vision, strategy, and roadmap across the company’s core platform and data products Build and scale a high-performing product team across platform, data, and applied AI initiatives Partner closely with engineering, data science, clinical, and commercial leadership to translate scientific and business priorities into executable product plans Define clear product objectives and measurable outcomes aligned with company-wide goals Drive product discovery processes, including customer research with biopharma partners, clinicians, and healthcare stakeholders Own prioritization and trade-off decisions across short-term delivery needs and long-term strategic platform development Ensure successful launch and adoption of enterprise-grade software solutions within regulated healthcare and life sciences environments Establish best practices for product management, roadmap communication, and cross-functional collaboration Work directly with executive leadership and board-level stakeholders to communicate product strategy and performance Support go-to-market initiatives by partnering with sales and marketing to clearly articulate product value propositions Recruit, mentor, and develop product leaders as the organization scales Foster a culture of accountability, curiosity, and data-driven decision-making across the product function Qualifications Bachelor’s degree in a technical, scientific, or related field; advanced degree (MBA, MS, PhD) is a plus 6-8+ years of experience in product management, including 3+ years in senior product leadership roles Experience building and scaling complex software products within TechBio, health tech, digital health, life sciences platforms, or AI-driven healthcare environments Strong understanding of regulated healthcare or biopharma workflows, including exposure to compliance, clinical data, or enterprise healthcare systems Demonstrated experience leading cross-functional teams spanning engineering, data science, and domain experts Proven ability to define and execute product strategy in fast-paced, high-growth environments Experience working with data-intensive platforms, AI/ML-enabled products, or scientific software tools Exceptional communication skills with the ability to translate complex scientific or technical concepts into clear business value Strong commercial intuition and experience working closely with enterprise customers or strategic partners Track record of hiring and developing high-performing product teams Comfortable operating both strategically and tactically in ambiguous, evolving environments Read Less
  • Senior Director, Cancer Immunology  

    - Alameda County
    SciPro is partnered with a well-funded, late-stage oncology biotech ad... Read More
    SciPro is partnered with a well-funded, late-stage oncology biotech advancing a pipeline of targeted cancer therapies. They are looking for a seasoned leader with deep expertise in immunology or oncology to help shape strategy, drive portfolio execution, and collaborate cross-functionally as programs progress toward regulatory submission and commercialization. They are focused on improving the outcomes in high unmet need for solid tumors such as lung, pancreatic, and colorectal cancers, with the goal of delivering next-generation targeted therapies where existing treatments have limited durability. They are growing to keep up with the demand of their progressing clinical trials as they move towards the goal of approval and launch. This role presents a unique opportunity to step into a strategic and scientific leadership position within Cancer Immunology, reporting into the Biology organization. The team is seeking a highly motivated, analytical thinker with a strong passion for scientific excellence and innovation, who can drive the discovery and advancement of novel immuno-oncology targets and modalities. This individual will lead a multidisciplinary team, define the scientific vision for Discovery Cancer Immunology, and oversee integration across both Discovery and Translational Cancer Immunology efforts. Main Responsibilities: Discovery Program Leadership Strategic Oversight: Lead Cancer Immunology discovery programs from project qualification through Development Candidate nomination. Drive the identification and validation of novel immuno-oncology targets, ensuring seamless progression of programs into Translational Cancer Immunology. Platform Modality Innovation: Oversee the development and optimization of experimental platforms, including in vitro and in vivo models, phenotypic screening, and advanced assay toolkits. Champion the exploration and implementation of new therapeutic modalities, such as TCEs, ADCs, and bispecifics. Scientific Integration Operational Excellence: Provide strategic oversight of scientific integration across Discovery and Translational Cancer Immunology, ensuring operational rigor, platform support, and alignment of resources. Leverage enabling functions and data-driven insights to enhance experimental design, reproducibility, and program execution. Promote the development and deployment of modern data systems and analytics to advance scientific and operational excellence, enabling the establishment of a digitally empowered Cancer Immunology team within the broader organization. Cross-functional Collaboration: Partner with Research Leadership to support advancement of programs from early discovery into the clinical development portfolio. Foster collaboration across multidisciplinary teams to ensure that discovery efforts, platform capabilities including data platforms, and translational priorities are coordinated and integrated. Team Leadership Mentorship: Lead, mentor, and inspire a multidisciplinary team of PhD and non-PhD scientists. Cultivate a culture of scientific excellence, innovation, and collaboration. External Engagement: Spearhead collaborations with academic partners and external organizations. Partner with key stakeholders to define publication strategies and support advancement of the company's scientific reputation in the field. Required Qualifications: Ph.D. in immunology, cancer biology, or a related discipline, with deep expertise in tumor immunology, immune-evasive oncogenic signaling pathways, and/or immunotherapy. Demonstrated track record of excellence in research, evidenced by high-impact publications. Industry Experience in oncology drug discovery and development, including experience with antibody-directed therapies such as T cell engagers, ADCs, or bispecific antibodies. Early discovery strategy experience is highly desirable. Proven ability to lead multidisciplinary teams and cross-functional projects, with excellent people management skills. Experience in project team leadership and mentoring scientists is strongly preferred. Strong strategic thinker capable of prioritizing initiatives, anticipating challenges, and executing effectively in a dynamic, high-energy environment. Rigorous, quantitative, and detail-oriented experimentalist. Thrives in a collaborative, interdisciplinary team setting. Excellent written and verbal communication skills, with the ability to influence and align diverse stakeholders. Preferred Qualifications: Experience with chemistry-based therapies, including small molecules or ADC payloads. Familiarity with bioinformatics-driven discovery and integrating computational insights into experimental design. Demonstrated proficiency with modern data platforms, machine learning approaches, and advanced analytics to support Cancer Immunology research and decision-making. Prior experience as a Program Team Leader, with a track record of driving cross-functional strategy and execution across discovery and development stages. Read Less
  • Staff Design Quality Engineer  

    - Alameda County
    Responsibilities: Ensure all design control activities for new and upd... Read More
    Responsibilities: Ensure all design control activities for new and updated products meet company procedures and global regulatory requirements. Lead risk management activities, including hazard analysis, FMEAs, and risk documentation. Support sterilization and biocompatibility assessments. Own and maintain design control documentation. Partner with R D, Regulatory, Manufacturing, and Project Management to ensure quality is built into every stage of product development. Maintain accurate test, validation, and risk records and report progress to leadership. Support regulatory submissions (e.g., 510(k), CE Mark). Lead root cause investigations and corrective actions related to design issues. Support complaint investigations, nonconformances, and CAPAs after product launch. Conduct DHF audits to ensure phase completion requirements are met. Review and approve engineering documents and test reports. Identify opportunities to improve product quality, reduce cost, and increase efficiency. Requirements Bachelor's degree in Engineering or related field. 10+ years of quality engineering experience in medical devices, including new product launches. Experience with sterilization and biocompatability Strong knowledge of design controls, risk management, and medical device regulations (FDA, ISO, IEC). Experience with verification validation (V V) and FMEAs. Strong problem-solving and statistical analysis skills (e.g., Minitab, JMP). Detail-oriented with strong documentation skills. Quality certifications (CQE, CSQE, Six Sigma) are a plus. Read Less
  • Lab Data Manager  

    - Hudson County
    Lab Data Manager Hybrid Jersey City, NJ or San Francisco, CA Position... Read More
    Lab Data Manager Hybrid Jersey City, NJ or San Francisco, CA Position The Lab Data Manager will be responsible for timely and high-quality management of local lab reference ranges supporting the client's portfolio including the loading of Lab Normal Ranges (LNR) within the EDC system and the management of LNR issue tracking and health status of a particular lab, site or study. Responsibilities Review and quality control (QC) the reference ranges provided by the site or, if applicable, other functional groups. Create lab normal range import file and uploads it into EDC local lab module. Be responsible for LNR issue tracking and maintaining health status at lab, site, and study level for communication to Data Management leadership or other cross functional teams. Manage local lab range units within the EDC system including change control process. Collaborate with Data Management colleagues, and study site personnel to continuously improve the collection and loading of LNR data. Provide LNR training for Data Management and other functions as required. Be responsible for the creation and maintenance of any Data Management owned controlled documents and provide SME knowledge to any cross functional controlled documents related to LNRs. Act as the LNR SME for Health Authority inspections and audits. Serve as a primary point of contact for internal and external study team members regarding local lab reference ranges. Serve as a backup for medical coding activities. Qualifications 6+ years of experience with a Bachelor's degree in a health related field (Chemistry, Nursing, etc.); or 4+ years of experience with a post graduate degree Proven experience in clinical data management gained from working at recognized clinical data management suppliers/vendors, reputable CRO(s) and/or a Sponsor environment working on multi-phase, multi-therapeutic (Oncology experience will be preferred) and diverse clinical trials from study initiation to completion and associated regulatory submission and inspection preparation. 3+ years of experience focused on the collection and maintenance of local lab reference ranges within standard clinical data management systems. Expertise with Lab analytes collected and tested in Oncology clinical trials is preferred. Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors. Sound knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management and local lab ranges. Strong knowledge and experience of EDC systems (Veeva CDMS preferred); demonstrated knowledge of Microsoft Office skills and well versed in industry trends and emerging technologies supporting data collection. Experience using a Local Lab Module within a standard EDC system is required. Strong project management, metrics analysis and reporting methodologies experience. Excellent oral and written communication skills and able to communicate effectively with senior management and cross-functional teams. Good knowledge of CDASH/CDISC (CDASH CRF Library implementation experience is preferred). Knowledge of submission requirements, [e.g. New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA)]. Read Less
  • Staff Design Quality Engineer  

    - Alameda County
    Responsibilities: Ensure all design control activities for new and upd... Read More
    Responsibilities: Ensure all design control activities for new and updated products meet company procedures and global regulatory requirements. Lead risk management activities, including hazard analysis, FMEAs, and risk documentation. Support sterilization and biocompatibility assessments. Own and maintain design control documentation. Partner with R D, Regulatory, Manufacturing, and Project Management to ensure quality is built into every stage of product development. Maintain accurate test, validation, and risk records and report progress to leadership. Support regulatory submissions (e.g., 510(k), CE Mark). Lead root cause investigations and corrective actions related to design issues. Support complaint investigations, nonconformances, and CAPAs after product launch. Conduct DHF audits to ensure phase completion requirements are met. Review and approve engineering documents and test reports. Identify opportunities to improve product quality, reduce cost, and increase efficiency. Requirements Bachelor's degree in Engineering or related field. 10+ years of quality engineering experience in medical devices, including new product launches. Experience with sterilization and biocompatability Strong knowledge of design controls, risk management, and medical device regulations (FDA, ISO, IEC). Experience with verification validation (V V) and FMEAs. Strong problem-solving and statistical analysis skills (e.g., Minitab, JMP). Detail-oriented with strong documentation skills. Quality certifications (CQE, CSQE, Six Sigma) are a plus. Read Less
  • Senior Director, Cancer Immunology  

    - Alameda County
    SciPro is partnered with a well-funded, late-stage oncology biotech ad... Read More
    SciPro is partnered with a well-funded, late-stage oncology biotech advancing a pipeline of targeted cancer therapies. They are looking for a seasoned leader with deep expertise in immunology or oncology to help shape strategy, drive portfolio execution, and collaborate cross-functionally as programs progress toward regulatory submission and commercialization. They are focused on improving the outcomes in high unmet need for solid tumors such as lung, pancreatic, and colorectal cancers, with the goal of delivering next-generation targeted therapies where existing treatments have limited durability. They are growing to keep up with the demand of their progressing clinical trials as they move towards the goal of approval and launch. This role presents a unique opportunity to step into a strategic and scientific leadership position within Cancer Immunology, reporting into the Biology organization. The team is seeking a highly motivated, analytical thinker with a strong passion for scientific excellence and innovation, who can drive the discovery and advancement of novel immuno-oncology targets and modalities. This individual will lead a multidisciplinary team, define the scientific vision for Discovery Cancer Immunology, and oversee integration across both Discovery and Translational Cancer Immunology efforts. Main Responsibilities: Discovery Program Leadership Strategic Oversight: Lead Cancer Immunology discovery programs from project qualification through Development Candidate nomination. Drive the identification and validation of novel immuno-oncology targets, ensuring seamless progression of programs into Translational Cancer Immunology. Platform Modality Innovation: Oversee the development and optimization of experimental platforms, including in vitro and in vivo models, phenotypic screening, and advanced assay toolkits. Champion the exploration and implementation of new therapeutic modalities, such as TCEs, ADCs, and bispecifics. Scientific Integration Operational Excellence: Provide strategic oversight of scientific integration across Discovery and Translational Cancer Immunology, ensuring operational rigor, platform support, and alignment of resources. Leverage enabling functions and data-driven insights to enhance experimental design, reproducibility, and program execution. Promote the development and deployment of modern data systems and analytics to advance scientific and operational excellence, enabling the establishment of a digitally empowered Cancer Immunology team within the broader organization. Cross-functional Collaboration: Partner with Research Leadership to support advancement of programs from early discovery into the clinical development portfolio. Foster collaboration across multidisciplinary teams to ensure that discovery efforts, platform capabilities including data platforms, and translational priorities are coordinated and integrated. Team Leadership Mentorship: Lead, mentor, and inspire a multidisciplinary team of PhD and non-PhD scientists. Cultivate a culture of scientific excellence, innovation, and collaboration. External Engagement: Spearhead collaborations with academic partners and external organizations. Partner with key stakeholders to define publication strategies and support advancement of the company's scientific reputation in the field. Required Qualifications: Ph.D. in immunology, cancer biology, or a related discipline, with deep expertise in tumor immunology, immune-evasive oncogenic signaling pathways, and/or immunotherapy. Demonstrated track record of excellence in research, evidenced by high-impact publications. Industry Experience in oncology drug discovery and development, including experience with antibody-directed therapies such as T cell engagers, ADCs, or bispecific antibodies. Early discovery strategy experience is highly desirable. Proven ability to lead multidisciplinary teams and cross-functional projects, with excellent people management skills. Experience in project team leadership and mentoring scientists is strongly preferred. Strong strategic thinker capable of prioritizing initiatives, anticipating challenges, and executing effectively in a dynamic, high-energy environment. Rigorous, quantitative, and detail-oriented experimentalist. Thrives in a collaborative, interdisciplinary team setting. Excellent written and verbal communication skills, with the ability to influence and align diverse stakeholders. Preferred Qualifications: Experience with chemistry-based therapies, including small molecules or ADC payloads. Familiarity with bioinformatics-driven discovery and integrating computational insights into experimental design. Demonstrated proficiency with modern data platforms, machine learning approaches, and advanced analytics to support Cancer Immunology research and decision-making. Prior experience as a Program Team Leader, with a track record of driving cross-functional strategy and execution across discovery and development stages. Read Less
  • Head of Product  

    - Suffolk County
    SciPro is partnered with a venture-backed TechBio company leveraging A... Read More
    SciPro is partnered with a venture-backed TechBio company leveraging AI and real-world data to transform how novel therapeutics are discovered, developed, and delivered. The company is building a scalable, data-driven platform that integrates multi-modal biological data, advanced analytics, and clinical insights to accelerate drug development and improve patient outcomes. This is a high-impact leadership opportunity to define and scale the product organization at the intersection of life sciences, AI/ML, and healthcare infrastructure within a fast-growing, deeply collaborative environment. Responsibilities Lead the overall product vision, strategy, and roadmap across the company's core platform and data products Build and scale a high-performing product team across platform, data, and applied AI initiatives Partner closely with engineering, data science, clinical, and commercial leadership to translate scientific and business priorities into executable product plans Define clear product objectives and measurable outcomes aligned with company-wide goals Drive product discovery processes, including customer research with biopharma partners, clinicians, and healthcare stakeholders Own prioritization and trade-off decisions across short-term delivery needs and long-term strategic platform development Ensure successful launch and adoption of enterprise-grade software solutions within regulated healthcare and life sciences environments Establish best practices for product management, roadmap communication, and cross-functional collaboration Work directly with executive leadership and board-level stakeholders to communicate product strategy and performance Support go-to-market initiatives by partnering with sales and marketing to clearly articulate product value propositions Recruit, mentor, and develop product leaders as the organization scales Foster a culture of accountability, curiosity, and data-driven decision-making across the product function Qualifications Bachelor's degree in a technical, scientific, or related field; advanced degree (MBA, MS, PhD) is a plus 6-8+ years of experience in product management, including 3+ years in senior product leadership roles Experience building and scaling complex software products within TechBio, health tech, digital health, life sciences platforms, or AI-driven healthcare environments Strong understanding of regulated healthcare or biopharma workflows, including exposure to compliance, clinical data, or enterprise healthcare systems Demonstrated experience leading cross-functional teams spanning engineering, data science, and domain experts Proven ability to define and execute product strategy in fast-paced, high-growth environments Experience working with data-intensive platforms, AI/ML-enabled products, or scientific software tools Exceptional communication skills with the ability to translate complex scientific or technical concepts into clear business value Strong commercial intuition and experience working closely with enterprise customers or strategic partners Track record of hiring and developing high-performing product teams Comfortable operating both strategically and tactically in ambiguous, evolving environments Read Less

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