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    Invivo Pharmacology Scientist

    Syngene
    2-8 years
    Not Disclosed
    Bangalore
    10 Jan. 29, 2025
    Job Description
    Job Type: Full Time Education: B.Sc,M.Sc,B.Pharma,M.Pharma,LifeScience Graduates 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

    Job Title: In vivo Pharmacology Scientist
    Location: Bangalore
    Date: 15 Jan 2025

    Company Overview:

    Syngene is an innovation-driven contract research, development, and manufacturing organization providing integrated scientific services from early discovery to commercial supply. We prioritize safety in all aspects of our operations, aligning safety with business performance and ensuring compliance with safety protocols and quality standards.

    Job Overview:

    The In vivo Pharmacology Scientist will be responsible for executing in vivo pharmacology experiments, focusing on disease models and mechanistic studies. This role involves independent and collaborative work in designing and performing efficacy experiments within the therapeutic area, as well as reporting and analyzing research outcomes. The ideal candidate will have hands-on experience with various disease models and animal handling techniques.

    Core Responsibilities:

    • Disease Models:
      • Execute disease models, including db/db, ob/ob, ZDF, Zucker, GK rat, and STZ models.
      • Work with obesity and dyslipidemia models, including DIO mice, DIO rats, hyperlipidemic hamsters, and hyperlipidemic guinea pigs.
    • Mechanistic Studies:
      • Conduct mechanistic studies, including OGTT, IVGTT, IPGTT, MMTT, LTT, and Euglycemic hyperinsulinemic clamps.
    • In vivo Efficacy Experiments:
      • Design and execute in vivo efficacy experiments independently or in collaboration with senior scientists and team members.
      • Perform various animal handling techniques (rodents and non-rodents), including dosing, bleeding, injections, and surgical procedures such as cannulation.
    • Research Analysis & Reporting:
      • Provide technical analysis and report outcomes of research related to the relevant therapeutic area.
      • Contribute to the preparation of study reports and communicate findings confidently in meetings.
    • Collaboration & Teamwork:
      • Collaborate effectively in a team-oriented environment, demonstrating organizational skills and the ability to work well with others.

    Required Qualifications:

    • Educational Qualification:
      • M. Pharm degree.
    • Experience:
      • 2-8 years of hands-on experience in in vivo pharmacology, specifically with disease models and mechanistic studies.
      • Experience with animal handling techniques, including dosing, injections, bleeding, and surgical procedures.

    Technical Skills:

    • Strong experience with disease models, particularly those relevant to obesity, dyslipidemia, and diabetes.
    • Expertise in performing mechanistic studies and handling laboratory animals (rodents and non-rodents).
    • Proficient in reporting research outcomes and analysis for relevant therapeutic areas.

    Behavioral Skills:

    • Teamwork:
      • Ability to work effectively as a team player and contribute to a collaborative environment.
    • Commitment:
      • Dedication to meeting study report deadlines and delivering high-quality results.
    • Adaptability:
      • Ability to adapt to changes in the dynamic lab environment and contribute to evolving project requirements.
    • Communication:
      • Clear and confident communication skills, with experience in presenting study reports and publications in peer-reviewed journals.

    Syngene Values:

    • Excellence: Commitment to high standards and continuous improvement.
    • Integrity: Upholding ethical standards and transparency.
    • Professionalism: Maintaining a professional approach in all aspects of work.

    Equal Opportunity Employer:

    Syngene is committed to providing equal employment opportunities (EEO) to all individuals regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, gender, sex, sexual orientation, gender identity, or any other characteristic protected by law. We also provide reasonable accommodations for qualified individuals with disabilities.

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