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Clinical Scientist - Neuroscience (Sr Manager)

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Bristol Myers Squibb

1mo ago

  • Job
    Full-time
    Junior Level
  • Research & Development
    Healthcare
  • Summit

AI generated summary

  • You need a Life Sciences degree, 2+ years in clinical science, GCP/ICH knowledge, basic data review skills, medical writing proficiency, and adaptability for project management. Travel may be required.
  • You will design and execute clinical trials, lead activities, develop documents, collaborate with teams, monitor data trends, and contribute to regulatory submissions and reports.

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)
  • 2+ years experience in clinical science, clinical research, or equivalent
  • Proficient 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)
  • 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)
  • Domestic and International travel may be required

Responsibilities

  • Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members within the assigned project to execute activities associated with the conduct
  • May serve as Clinical Trial Lead for one or more trials
  • May lead or support trial level activities for one or more trials with the necessary supervision
  • May co-lead study team meetings in partnership with GDO protocol manager and collaborate with cross-functional study team members
  • 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 - Neuroscience at Bristol Myers Squibb?

The primary role involves providing scientific expertise to design and deliver clinical studies and programs, leading clinical trial activities, collaborating with cross-functional teams, and liaising with external partners like Key Opinion Leaders (KOLs).

What qualifications are required for this position?

A degree in Life Sciences (MD, PhD, Pharm D, MS, RN, or other scientific field preferred) is required, along with 2+ years of experience in clinical science, clinical research, or an equivalent field.

What are the expected responsibilities for this position?

Responsibilities include collaborating with external partners, developing protocol documents, conducting literature reviews, monitoring clinical data, and contributing to clinical study reports and regulatory submissions.

Is travel required for this position?

Yes, domestic and international travel may be required.

What is the expected compensation range for California-based candidates?

The starting compensation for California-based candidates is in the range of $144,000 - $180,000, plus incentive cash and stock opportunities, based on eligibility.

Are there opportunities for professional growth within this role?

Yes, Bristol Myers Squibb offers opportunities to grow and thrive through unique work experiences and collaboration with high-achieving teams.

What type of work environment does BMS provide?

BMS provides a flexible work environment that values balance and offers a wide variety of competitive benefits aimed at supporting employees in their personal and professional goals.

Does BMS have a diverse work culture?

Yes, BMS values diversity and inclusion, and promotes an inclusive culture where individual talents and unique perspectives are encouraged.

What is the policy regarding COVID-19 vaccinations for employees?

BMS strongly recommends that all employees be fully vaccinated for COVID-19 and keep up to date with COVID-19 boosters.

Are there options for work-life balance benefits?

Yes, BMS offers various work-life programs including paid vacation, parental leave, volunteer days, and support services for family care.

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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.