Sr Manager Clinical Research Scientist
Sr Manager Clinical Research Scientist
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Job Description
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. Taihos 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 cuttingedge 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 worldclass clinical development organization and stateoftheart facilities: these and other resources empower us to innovate and touch the lives of more and more patients. Its 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 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 of key tasks involved in the design conduct monitoring and review of study data analysis and reporting of clinical trials.
Performance Objectives:
- 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.
- Use scientific expertise to support the creation of relevant highquality clinical documents such as study protocols and clinical study reports (CSRs) investigator brochures DSUR NDA/MAA registration documents and publications.
- 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.
- Keeps the latest knowledge in clinical development through publications and scientific conferences and leverages the knowledge for designing and summarizing clinical studies.
- Keeps Sr. Medical Director current on status of clinical trials and provides ongoing risk assessments for the study conduct and operational risks.
- Performs other duties as required.
Education/Certification Requirements:
- Masters level degree in pharmaceutical or related medical science is preferred. Bachelors level candidates with substantive prior pharmaceutical experience will also be considered.
Knowledge Skills and Abilities:
- 35 years of experience in drug development in pharmaceutical industry.
- 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.
- Ability to critically review and interpret Clinical data.
The pay range for this position at commencement of employment is expected to be between $165K $195K 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 jobrelated knowledge skills and experience. The total compensation package for this position may also include other elements including a signon 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 atwill 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.
#LocationPrincetonNJ #LIHybrid
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 . 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.
Other details
- Travel 25
Required Experience:
Manager
Employment Type
Full-Time
