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Remote Senior Scientist in Safety Data | WFH at Get It Recruit - Information Technology

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 
Illinois (USA), United States

Offer summary

Qualifications:

Master's degree in health science or related field with 1-2 years experience, Bachelor's degree with 2+ years in clinical, pharmaceutical, or safety roles.

Key responsabilities:

  • Collaborate with teams to evaluate safety signals
  • Analyze clinical trials and safety data for decision-making
  • Develop strategies to manage safety risks
  • Prepare summaries of safety findings for stakeholders
  • Maintain safety documentation and ensure compliance
Get It Recruit - Information Technology logo
Get It Recruit - Information Technology Human Resources, Staffing & Recruiting TPE https://www.get.it/
2 - 10 Employees
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Job description

Make a Difference in Patient Safety

Job Overview

We are searching for a dedicated and meticulous Senior Scientist specializing in Safety Data to join our remote team. In this pivotal role, you will significantly contribute to ensuring the safety of our products, thereby enhancing patient well-being throughout their lifecycle.

Key Responsibilities

  • Collaborate with interdisciplinary teams to proactively identify and evaluate potential safety signals associated with assigned products.
  • Conduct comprehensive analysis of data derived from clinical trials, safety databases, and relevant scientific literature to inform decision-making.
  • Work alongside colleagues to devise strategies for managing identified safety risks and execute suitable mitigation measures.
  • Draft clear and concise written and verbal summaries of safety findings for various stakeholders, including senior management and regulatory bodies.
  • Assist in the creation and upkeep of essential safety documentation, such as Clinical Safety Reports and Risk Management Plans.
  • Stay informed on the latest pharmacovigilance regulations and industry best practices to ensure compliance and excellence.

Required Skills

  • Strong comprehension of the drug development process, encompassing clinical trials, regulatory requirements, and post-marketing support.
  • Exceptional analytical capabilities with proficiency in data analysis tools.
  • Effective communication skills, both written and oral, with the capacity to convey complex scientific information to diverse audiences.
  • Outstanding teamwork and collaboration skills, enabling success in a fast-paced, multidisciplinary environment.
  • Proficiency in Microsoft Word and Excel, complemented by basic project management abilities.

Qualifications

  • A Master’s degree in a health science discipline (e.g., Pharmacy, Epidemiology, Nursing) accompanied by 1-2 years of relevant experience, or a Bachelor’s degree with 2+ years of experience in clinical, pharmaceutical, or safety roles.

Career Growth Opportunities

We are committed to fostering your professional development and offer continuous learning opportunities aimed at advancing your career within our esteemed organization.

Company Culture And Values

Our organization champions collaboration and teamwork, creating a multidisciplinary environment that fuels innovation while maintaining a steadfast commitment to patient safety.

Why Join Us?

Contribute to impactful work that directly affects patient safety and well-being. Become part of a dedicated team that is passionate about making a difference. Apply today!

Employment Type: Full-Time

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Human Resources, Staffing & Recruiting
Spoken language(s):
Check out the description to know which languages are mandatory.

Other Skills

  • Teamwork
  • Analytical Skills
  • Microsoft Word
  • Microsoft Excel
  • Verbal Communication Skills

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