Logo of Huzzle

Home

Matches

Explore

Manage

Clinical Scientist, Cell Therapy

image

Bristol Myers Squibb

1mo ago

  • Job
    Full-time
    Entry Level
  • Madison

AI generated summary

  • You must have expertise in cell therapy, strong analytical skills, and a background in clinical research to support innovative treatment development.
  • You will conduct experiments, analyze data, collaborate with cross-functional teams, and support development of cell therapies, ensuring compliance with protocols and regulations.

Requirements

  • Degree Requirements
  • - Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or other scientific field preferred). Appropriate for new entrance to pharma (post fellowship/new to industry)
  • Experience Requirements
  • - Basic knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations
  • - Ability to understand assigned protocol(s) and their requirements
  • - Basic knowledge skills to support program-specific data review and trend identification
  • - Intermediate medical writing skills and medical terminology
  • - Basic planning/project management skills (develop short range plans that are realistic and effective)
  • Key Competency Requirements
  • - Detail-oriented with commitment to quality
  • - Basic knowledge of disease area, compound, current clinical landscape
  • - Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees
  • - Intermediate 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)
  • - Intermediate 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.

Responsibilities

  • Collaborate and liaise with external partners (e.g., KOLs)
  • Seek out and enact best practices with instruction
  • Provide regular and timely updates to manager/management as requested
  • Develop Protocol and ICF documents / amendments and present these to governance committee and development team meetings as required
  • Conduct literature review
  • Submit clinical documents to TMF
  • Develop site and CRA training materials and present these at SIVs and Investigator meetings
  • Review clinical narratives
  • Monitor clinical data for specific trends
  • Develop Data Review Plan in collaboration with Data Management
  • Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming
  • Submit clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission.)

FAQs

What is the primary role of a Clinical Scientist in Cell Therapy at Bristol Myers Squibb?

The primary role involves collaborating with external partners, developing clinical documents, conducting literature reviews, monitoring clinical data, and contributing to regulatory submissions, all aimed at supporting the advancement of cell therapy and transforming patient lives.

What qualifications are required to apply for this position?

A degree in Life Sciences (MD, PhD, Pharm D, MS, RN, or other scientific fields) is preferred. The role is also appropriate for recent graduates or those new to the pharmaceutical industry post-fellowship.

What kind of experience is necessary for this role?

Basic knowledge of GCP/ICH guidelines, the drug development process, study design, and medical terminology is required. Candidates should also have some experience in planning or project management.

Are there opportunities for travel in this position?

Yes, domestic and international travel may be required as part of the responsibilities associated with the Clinical Scientist role.

What type of skills are emphasized for this position?

The position emphasizes detail orientation, adaptability, intermediate critical thinking skills, basic project management skills, and proficiency in Microsoft Office applications.

How does Bristol Myers Squibb support work-life balance for its employees?

Bristol Myers Squibb offers a variety of competitive benefits, including flexible work schedules, generous vacation, and paid leave programs, along with wellness programs and financial resources to support employees' personal and professional goals.

What is the compensation range for the Clinical Scientist role?

The starting compensation for this job ranges from $156,000 to $208,000, plus potential incentive cash and stock opportunities based on eligibility.

What type of work environment can employees expect at Bristol Myers Squibb?

Employees can expect a challenging and meaningful work environment that emphasizes diversity, collaboration, and innovation, all while working towards the shared goal of transforming patient lives through science.

Is there any specific training required for this role?

While specific training will be provided for the role, candidates should possess basic knowledge in areas such as clinical operations, medical writing, and database management to support their responsibilities effectively.

How does Bristol Myers Squibb ensure inclusivity in its workplace?

Bristol Myers Squibb fosters an inclusive culture by promoting diversity in clinical trials, empowering employees to apply their unique talents and perspectives, and ensuring reasonable accommodations are available for individuals with disabilities.

What are the specific responsibilities related to data management in this role?

Responsibilities include developing Data Review Plans, monitoring clinical data for trends, ensuring Case Report Form (CRF) design supports data collection, and collaborating with Data Management/Programming on these initiatives.

How does Bristol Myers Squibb handle applications from individuals with prior convictions?

Bristol Myers Squibb will consider qualified applicants with arrest and conviction records in accordance with applicable laws in the area of employment.

Bristol Myers Squibb

Manufacturing & Electronics
Industry
10,001+
Employees

Mission & Purpose

At Bristol Myers Squibb, we work every day to transform patients’ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers you’ll experience. Join us and pursue innovative ideas alongside some of the brightest minds in biopharma, collaborating with a team rich in diversity of experiences, and perspectives. We have built a sustainable pipeline of potential therapies and are leveraging translational medicine and data analytics to understand how we can deliver the right medicine to the right patient, at the right time, to achieve the best outcome. Whether in a scientific, business or supporting function, a career at BMS means you’ll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, you’ll be on the cutting edge of powerful innovation in oncology, hematology, immunology, cardiovascular disease, and fibrosis, with colleagues united in the mission to help patients. Through the Bristol Myers Squibb Foundation, we also promote health equity and seek to improve health outcomes of populations disproportionately affected by serious diseases and conditions. Our mission is to give new hope to help patients prevail over serious disease – it drives everything we do.