Position Summary:The Senior Manager, Clinical Research Scientist assists in designing, executing, and reporting Phase 1-3 clinical oncology trials. The role supports the medical monitor with key tasks related to trial design, conduct, monitoring, analysis, and reporting.Performance Objectives:<ol><li>Collaborate with team members (Medical Monitors, Project Managers, Clinical Operations, Data Management, Biostatistics, PV, PK, Biomarkers, Medical Writing) to deliver high-quality trial results.</li><li>Use scientific expertise to create essential clinical documents (study protocols, CSRs, investigator brochures, DSUR, NDA/MAA registration documents, publications).</li><li>Review and summarize clinical data to ensure study quality and protocol compliance.</li><li>Stay updated on clinical development knowledge and apply it to study design and summaries.</li><li>Inform the Sr. Medical Director about trial status and provide risk assessments.</li><li>Perform other duties as required. Travel up to 25%.</li></ol>Education/Certification Requirements:<ol><li>Preferred: Master's degree in pharmaceutical or related medical science.</li></ol>Knowledge, Skills, and Abilities:<ol><li>3-5 years of drug development experience in the pharmaceutical industry.</li><li>At least 2 years in oncology with exposure to clinical development (reviewing data quality, protocols, CSRs, investigator brochures, DSUR, NDA/MAA documents, publications).</li><li>Ability to critically review and interpret clinical data.</li></ol>
#J-18808-Ljbffr

Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy. We invite you to join us. Hybrid Employee Value Proposition: At Taiho Oncology, we are dedicated to transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager, Clinical Research Scientist, you will play a pivotal role in our mission, leveraging your expertise to drive innovative clinical research and contribute to groundbreaking therapies. We offer a collaborative and inclusive work environment where your ideas and contributions are valued. Join us to advance your career, work with passionate and skilled professionals, and make a meaningful impact on the fight against cancer. At Taiho Oncology, you will find purpose, growth, and the opportunity to be at the forefront of cancer research. Position Summary: The Senior Manager, Clinical Research Scientist has responsibility assisting in design, execution and reporting of current and future clinical oncology trials ranging from phase 1 - 3. Additionally, this role position supports the responsible medical monitor in the execution of key tasks involved in the design, conduct, monitoring, analysis and reporting of clinical trials. Performance Objectives: 
<ul>
<li>Collaborates with other key team members (Medical monitor, Project Manager, Clinical Operations, Data Management, Biostatistics, PV, PK, Biomarkers and Medical Writing etc.), to deliver high quality clinical trial results.</li>
<li>Use scientific expertise to support the creation of relevant high-quality clinical documents such as study protocols and clinical study reports (CSRs), investigator brochures, DSUR, NDA/MAA registration documents and publications.</li>
<li>Reviews and summarizes ongoing clinical data (from EDC and listings) to monitor the quality of the study, ensure clean data flow into the study database and compliance with the protocol.</li>
<li>Keeps the latest knowledge in clinical development through publications and scientific conferences and leverages the knowledge for designing and summarizing clinical studies.</li>
<li>Keeps Sr. Medical Director current on status of clinical trials and provides ongoing risk assessments for the study conduct and operational risks.</li>
<li>Performs other duties as required.</li>
<li>Travel requirements: up to 25%</li>
</ul> Education/Certification Requirements: 
<ul>
<li>Masters level degree in pharmaceutical or related medical science is preferred.</li>
<li>Bachelor’s level candidates with substantive prior pharmaceutical experience will also be considered.</li>
</ul> Knowledge, Skills, and Abilities: 
<ul>
<li>3-5 years of experience in drug development in pharmaceutical industry.</li>
<li>At least 2 years in drug development industry in oncology and with previous exposure to clinical development, such as reviewing of the quality of ongoing and final clinical study data, protocols and CSRs, investigator brochures, DSUR, NDA/MAA registration documents and publications.</li>
<li>Ability to critically review and interpret Clinical data.</li>
</ul> The pay range for this position at commencement of employment is expected to be between $155,550 and $183,000 annually. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, commissions, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. #LI-Hybrid Equal Opportunity Employer Information: Taiho Oncology is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, veteran status, gender identity, genetic information, or any other characteristic protected by federal, state, or local law. Any applicant who, because of a disability, needs an accommodation or assistance in completing an application or at any time during the application process, please email People@taihooncology.com. Taiho Oncology also provides reasonable accommodations to employees with disabilities consistent with our obligations under the law. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment qualified applicants with arrest and conviction records. The incumbent in this position may be required to perform other duties, as assigned.
#J-18808-Ljbffr

<div>
<h3>Job Description:</h3>
A Sr. Research Scientist-Medical Imaging Analysis position is available at EDDA Technology, Princeton, NJ. Responsibilities include:
<ul>
<li>Design, implementation, and verification of deep learning algorithms for 3D and 2D segmentation and registration problems on medical images;</li>
<li>Define, develop and validate clinical solutions;</li>
<li>Fast prototyping of image and video analysis product modules;</li>
<li>Collaborate closely with clinical customers to solve real-world problems;</li>
<li>Conforming to the Company’s standard/procedure of product development;</li>
<li>Efficiently communicating with project managers and team members on the execution;</li>
<li>Other job responsibilities as assigned by the management.</li>
</ul>
<h3>Minimum Qualifications:</h3>
<ul>
<li>Strong background in Deep Learning and/or Medical Image Analysis;</li>
<li>Coding skills and ability to quickly prototype Deep Learning models is a must;</li>
<li>Strong algorithm development skills with in-depth knowledge on medical image analysis/segmentation, image registration, computer vision, deep learning, real-time processing, and GPU programming;</li>
<li>3+ years of experience in the related fields preferred, with excellent software engineering skills in using C/C++; Other software skills preferred include Python, Pytorch, Tensor Flow, and Keras;</li>
<li>Experience and skills in working with large language models (LLMs) and large vision models (LVMs)</li>
<li>Experience in processing ultrasound images a plus;</li>
<li>Strong problem-solving skills with quick implementation and verification; Strong team player and highly self-motivated individual with desire and ability to learn quickly;</li>
<li>Written and verbal communication skills in English are required;</li>
<li>PhD in CE/EE/CS/Bio-Engineering.</li>
</ul>
<h3>Desired Qualifications:</h3>
<ul>
<li>Knowledge in human anatomy and interpretation of medical images a plus;</li>
<li>Hands-on experience and knowledge in DICOM a plus;</li>
</ul>
<h3>Company Introduction:</h3>
Excellent opportunity with a dynamic, growing medical technology solution company.
EDDA Technology is an innovative leader in the rapidly growing field of intelligent robotic solutions for precision surgery. Pioneering a “fully quantitative, interactive” approach to intelligent imaging analytics and robotic integration, the company has built a proprietary technology platform to facilitate pre-surgical planning and simulation, intra-operative navigation, post-operative evaluation. With its end-to-end enabling platform, EDDA’s goal is to form a comprehensive ecosystem of clinical practice, connection, and education to support physicians and patient management in all tiers of hospitals. IQQA is a registered trademark of EDDA Technology. (www.eddatech.com)
<h3>Compensation/Benefits:</h3>
EDDA offers a competitive salary, performance-based incentive stock options, and excellent benefits including medical and dental insurance, vision care, 401k plan, section 125 health and dependent care (flexible spending) accounts, and paid vacations. The company sponsors the H1-B application.
Send applications to: hiring@edda-tech.com
</div>
#J-18808-Ljbffr

A Sr. Research Scientist-Medical Imaging Analysis position is available at EDDA Technology, Princeton, NJ. Responsibilities include:
<ul>
<li>Design, implementation, and verification of deep learning algorithms for 3D and 2D segmentation and registration problems on medical images;</li>
<li>Define, develop and validate clinical solutions;</li>
<li>Fast prototyping of image and video analysis product modules;</li>
<li>Collaborate closely with clinical customers to solve real-world problems;</li>
<li>Conforming to the Company’s standard/procedure of product development;</li>
<li>Efficiently communicating with project managers and team members on the execution;</li>
<li>Other job responsibilities as assigned by the management.</li>
</ul>
Candidates shall meet part of the below qualifications:
<ul>
<li>Strong background in Deep Learning and/or Medical Image Analysis;</li>
<li>Coding skills and ability to quickly prototype Deep Learning models is a must;</li>
<li>Strong algorithm development skills with in-depth knowledge on medical image analysis/segmentation, image registration, computer vision, deep learning, real-time processing, and GPU programming;</li>
<li>3+ years of experience in the related fields preferred, with excellent software engineering skills in using C/C++; Other software skills preferred include Python, Pytorch, Tensor Flow, and Keras;</li>
<li>Experience and skills in working with large language models (LLMs) and large vision models (LVMs);</li>
<li>Experience in processing ultrasound images a plus;</li>
<li>Strong problem-solving skills with quick implementation and verification; Strong team player and highly self-motivated individual with desire and ability to learn quickly;</li>
<li>Written and verbal communication skills in English are required;</li>
<li>PhD in CE/EE/CS/Bio-Engineering.</li>
</ul>
Desired qualifications:
<ul>
<li>Knowledge in human anatomy and interpretation of medical images a plus;</li>
<li>Hands-on experience and knowledge in DICOM a plus;</li>
</ul>
Company Introduction:
EDDA Technology is an innovative leader in the rapidly growing field of intelligent robotic solutions for precision surgery. Pioneering a “fully quantitative, interactive” approach to intelligent imaging analytics and robotic integration, the company has built a proprietary technology platform to facilitate pre-surgical planning and simulation, intra-operative navigation, post-operative evaluation. With its end-to-end enabling platform, EDDA’s goal is to form a comprehensive ecosystem of clinical practice, connection, and education to support physicians and patient management in all tiers of hospitals.
Compensation/ Benefits:
EDDA offers a competitive salary and excellent benefits including medical and dental insurance, vision care, 401k plan, section 125 health and dependent care (flexible spending) accounts, and paid vacations. The company sponsors the H1-B application.
Send applications to: hiring@edda-tech.com
Job Type: Full-time
Pay: From $120,000.00 per year
Benefits:
<ul>
<li>401(k)</li>
<li>Dental insurance</li>
<li>Flexible spending account</li>
<li>Health insurance</li>
<li>Health savings account</li>
<li>Paid time off</li>
<li>Parental leave</li>
<li>Referral program</li>
<li>Relocation assistance</li>
<li>Vision insurance</li>
</ul>
Schedule:
<ul>
<li>Monday to Friday</li>
</ul>
Education:
<ul>
<li>Doctorate (Required)</li>
</ul>
Experience:
<ul>
<li>C++: 3 years (Required)</li>
<li>TensorFlow: 3 years (Required)</li>
<li>Keras: 3 years (Required)</li>
<li>Large Language Models: 1 year (Preferred)</li>
<li>Large Vision Models: 1 year (Preferred)</li>
<li>Medical Image Analysis/Segmentation: 1 year (Preferred)</li>
<li>Image Registration: 1 year (Preferred)</li>
<li>Computer vision: 1 year (Preferred)</li>
<li>DICOM: 1 year (Preferred)</li>
</ul>
Ability to Relocate:
<ul>
<li>Princeton, NJ 08540: Relocate with an employer provided relocation package (Required)</li>
</ul>
Work Location: In person
#J-18808-Ljbffr

Research Scientist Jobs in Princeton, NJ

Sr Manager Clinical Research Scientist
December 11, 2024

Sr Manager Clinical Research Scientist
December 10, 2024

Sr Research Scientistmedical Imaging Analysis
December 10, 2024

Sr Research Scientist
December 9, 2024

Quick filters

Top companies

Research Scientist Jobs in Princeton, NJ

Sr Manager Clinical Research ScientistDecember 11, 2024

Sr Manager Clinical Research ScientistDecember 10, 2024

Sr Research Scientistmedical Imaging AnalysisDecember 10, 2024