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    Associate Clinical Scientist, Oncology - Princeton, United States - BioSpace

    BioSpace
    BioSpace Princeton, United States

    3 weeks ago

    BioSpace background
    Description
    Job Details

    Working with Us
    Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

    Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: .

    The Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs.

    Position Summary / Objective
    • Supports execution of assigned clinical trial activities and works closely with Clinical Scientist to execute activities associated with trial conduct
    • Supports trial level activities for one or more trials with the necessary supervision
    Position Responsibilities
    • Seek out and enact best practices with instruction
    • Provide regular and timely updates to manager/management as requested
    • Support development of Protocol and ICF documents / amendments
    • Conduct literature review. Support submission of clinical documents to TMF
    • Support development of site and CRA training materials
    • Review clinical narratives
    • Collaborate cross-functionally to monitor clinical data for specific trends
    • Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming
    Degree Requirements
    • Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field preferred)
    Experience Requirements
    • Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations
    • Basic knowledge of disease area, compound, and current clinical landscape
    Key Competency Requirements
    • Detail-oriented with commitment to quality
    • Critical thinking and problem-solving skills
    • Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism)
    • Proficient skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., Pt Profiles, report generating tools)
    Travel Required
    • Domestic and International travel may be required
    If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

    Uniquely Interesting Work, Life-changing Careers
    With a single vision as inspiring as Transforming patients' lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

    On-site Protocol

    BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

    Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

    BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.

    BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

    BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

    Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.


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