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    Research Associate - Compatibility

    Baxter
    0-2 years
    Not Disclosed
    Remote, USA
    10 Nov. 20, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    This is where you save and sustain lives

    At Baxter, we are united by our mission. No matter your role, your work has a positive impact on people worldwide. You'll feel a deep sense of purpose as we improve outcomes for millions of patients.

    Baxter’s products and therapies are used in nearly every hospital globally, in clinics, and at home. For over 85 years, we have pioneered medical innovations that transform healthcare.

    Together, we create a place where we thrive, inspire each other, and do our best work.

    Join us at the intersection of saving and sustaining lives—where your purpose drives our mission forward.

    Your Role at Baxter

    Baxter is looking for a seasoned R&D Research Associate III with expertise in designing and leading Compatibility studies. This position will support our Parenteral Nutrition admixtures compatibility studies, directly contributing to our mission of saving and sustaining lives.

    What You'll Do

    As an R&D Research Associate III, you will play a key role in supporting the Nutrition Compatibility team in daily activities, including:

    • Designing and overseeing admixture/compatibility studies.
    • Purchasing products needed for study execution and coordinating shipment to testing labs.
    • Organizing study execution and interpreting experimental data.
    • Writing comprehensive protocols and reports.
    • Ensuring compliance with quality system requirements, GMP/GDP standards, and environmental, health, and safety (EHS) guidelines.
    • Participating in the review of analytical procedures for compatibility studies.
    • Demonstrating strong communication skills, attention to detail, and the ability to collaborate effectively with cross-functional teams.

    What You'll Bring

    • Master's degree with 3-5 years of experience in a relevant scientific field (chemistry, biochemistry, pharmaceutical sciences, etc.), or PhD with 0-3 years of experience.
    • Proficiency in laboratory/technical/analytical, writing, and computer skills.
    • Strong ability to design studies, analyze scientific results, and draw conclusions from lab data.
    • Experience organizing, assessing, and clearly communicating complex information.
    • Ability to prioritize assignments and meet project schedules.
    • Strong commitment to quality, attention to detail, and flexibility in a dynamic work environment.
    • Leadership skills and the ability to work well with virtual and cross-functional teams.
    • Experience in project management and global teams is a plus.

    Benefits of Working at Baxter

    Baxter offers a competitive total compensation package, with opportunities for professional development. We place a high value on work-life balance and foster a diverse, inclusive environment.

    Equal Opportunity Employer

    Baxter is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

    Reasonable Accommodations

    Baxter is committed to providing reasonable accommodations to applicants with disabilities. If you require accommodation during the application process, please inform us of your needs.

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