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    Senior Consultant

    Iqvia
    5+ years
    Not Disclosed
    Gurgaon
    10 Dec. 26, 2024
    Job Description
    Job Type: Full Time Education: MSc./M. Pharm/PhD 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: Senior Consultant – Evidence Synthesis Research
    Location: IQVIA Laboratories

    About IQVIA:
    IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We connect data, technology, and expertise to help accelerate the development and commercialization of innovative medical treatments that improve patient outcomes worldwide. To learn more, visit IQVIA Careers.

    Role Overview:
    We are seeking an experienced Senior Consultant to lead methodologically rigorous evidence synthesis research projects. This role involves overseeing the work of junior staff, managing overall projects, and ensuring that research outcomes exceed client expectations. You will work both independently and as part of a team, providing leadership and problem-solving solutions, while managing project timelines and client communications. This is an exciting opportunity to engage with cutting-edge methodologies, including systematic literature reviews (SLRs), meta-analysis, and network meta-analysis (NMA).

    Key Responsibilities:

    • Evidence Synthesis & Research:

      • Lead the implementation of SLRs, including developing search strategies, creating protocols, screening, data extraction, and quality control processes.
      • Synthesize data both qualitatively and quantitatively using statistical methods, including Bayesian analysis.
      • Write reports and create presentations (slide decks) to clearly explain methods, results, and interpretations.
      • Prepare proposals, including conducting scoping searches and articulating both qualitative and quantitative methods.

    • Project Management & Client Liaison:

      • Assist with overall project management, ensuring all deliverables are completed on time and to a high standard.
      • Liaise with clients, attending internal and client calls to present findings and updates.
      • Collaborate with clients to understand their business needs and develop customized research solutions.
      • Manage and supervise junior staff to ensure high-quality outputs and timely completion of tasks.

    • Team Leadership & Staff Management:

      • Oversee junior staff, ensuring quality work and providing mentorship and guidance.
      • Perform detailed quality checks on team deliverables, ensuring minimal errors.

    Qualifications & Experience:

    • Essential Qualifications:

      • Master's degree in Epidemiology, Pharmacology, Public Health, Biostatistics, or another related health sciences field.
      • 5+ years of experience in evidence synthesis research, preferably in a consulting, pharmaceutical, healthcare, or academic environment.
      • Proficiency in statistical software such as R, SAS, or STATA.

    • Preferred Experience:

      • PhD in Epidemiology, Public Health, or Biostatistics (or related fields).
      • Experience in network meta-analysis (NMA), Bayesian statistical analysis, and diagnostic steps for these methods.

    Skills & Knowledge:

    • Technical Skills:

      • Solid understanding of SLR concepts, guidelines, and required rigor.
      • Substantial experience conducting meta-analysis, NMA, or Bayesian analysis independently.
      • Proficiency in PowerPoint, Excel, and Word for presentation and reporting.

    • Personal Attributes:

      • Exceptional attention to detail, even under pressure.
      • Strong ability to interpret statistical results in observational and trial study designs.
      • Excellent communication skills, both written and spoken, with the ability to present complex information clearly to clients and teams.
      • Ability to work collaboratively within a global team and manage cross-time-zone communication effectively.
      • Strong problem-solving skills and time management expertise.

    What We Offer:

    • Competitive salary and benefits package.
    • A dynamic and inclusive work environment with global collaboration.
    • Opportunities for career development and professional growth within a leading company in clinical research.

    Equal Opportunity Employment:
    IQVIA is an equal opportunity employer committed to promoting diversity and inclusion. We provide equal employment opportunities for all, including veterans and candidates with disabilities. For more information, visit IQVIA Equal Opportunity.

    COVID-19 Vaccination Requirement:
    IQVIA may require employees to meet specific COVID-19 vaccination status requirements. For more details, visit COVID-19 Vaccine Status.

    Apply Now to join our innovative and passionate team in advancing healthcare worldwide!

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