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Associate/Senior Associate/Manager - Community-Based Research (Cbr)

3+ years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, 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: Associate/Senior Associate/Manager - Community-Based Research (CBR)
Location: Cork, Ireland
Category: Research & Development
Job Type: Full-Time, Regular
Job ID: R-75669

About Lilly:

At Lilly, we are driven by a mission to unite caring with discovery to make life better for people around the world. As a global healthcare leader headquartered in Indianapolis, Indiana, we are focused on discovering and delivering life-changing medicines, improving the understanding and management of disease, and giving back to our communities. We encourage an inclusive and diverse work environment where we strive to ensure the well-being and professional development of our employees.

Role Overview:

The Community-Based Research (CBR) team within Central Clinical Services and Innovation (CCSI) is focused on advancing clinical trials by creating novel solutions that increase accessibility, reduce burden, and enhance trial execution. This team works with multiple stakeholders to implement strategies that engage community-based locations for clinical program activities, increasing diversity and promoting awareness for clinical research.

The Community-Based Delivery Associate plays a key role in driving the implementation of solutions that facilitate the delivery of clinical program activities within communities. This includes leveraging processes, protocols, and education to identify clinical research participants, enhance health care options, and support the advancement of scientific innovation for drug development.

Key Responsibilities:

  • Operational Delivery: Support the implementation of Community-Based Delivery strategies and solutions to increase accessibility and promote awareness of clinical research across global communities.

  • Collaboration: Work closely with cross-functional teams (e.g., Clinical Design, Delivery, Analytics) to understand clinical program objectives and develop operational plans to ensure timely and efficient execution.

  • Vendor and Stakeholder Management: Oversee vendor performance, ensure deliverables are met, and resolve issues promptly. Foster strong relationships with business partners and vendors to ensure the smooth implementation of community-based delivery strategies.

  • Tracking and Reporting: Monitor and track performance metrics related to the community-based delivery strategy, including budgets, vendor management, and technology platform usage, and provide regular reports.

  • Continuous Improvement: Identify opportunities for process improvements and automation to reduce cycle time, increase efficiency, and ensure the success of community-based delivery strategies.

  • Inspection Readiness: Maintain a state of inspection readiness, preparing for internal and external inspections and supporting alternative site locations in readiness initiatives.

  • Innovation and Collaboration: Actively contribute to fostering an inclusive and innovative work culture, collaborating with study teams, research personnel, and vendors to optimize strategy delivery and enhance the participant experience.

Qualifications:

  • Education: A Bachelor’s degree in Life Sciences, Clinical Drug Development, or a related healthcare field is required.

  • Experience: At least 3 years of experience in clinical drug development, healthcare, or a related field.

  • Skills:

    • Strong interpersonal and relationship-building skills with the ability to work cross-functionally and lead teams to achieve results.
    • Knowledge of GxP regulations (GMP/GDP, GCP) and familiarity with clinical research guidelines.
    • Ability to adapt quickly to changing business priorities and complex environments.
    • Excellent verbal and written communication skills for effective collaboration and reporting.
  • Additional Preferences:

    • Knowledge of emerging healthcare services and capabilities for clinical research.
    • Understanding of country regulatory guidelines for clinical research.
    • Strong problem-solving, critical thinking, and ambiguity navigation skills.

Why Join Lilly?

  • Inclusive Work Environment: We are committed to fostering an inclusive, innovative, and diverse workplace culture.

  • Employee Benefits: Competitive salary, healthcare, pension, wellness programs, and more.

  • Professional Development: We offer opportunities for training, career growth, and educational assistance to help you thrive in your role.

Equal Opportunity Employer:

Lilly is dedicated to ensuring equal opportunities in the workplace and is committed to accommodating individuals with disabilities. If you need assistance with submitting your resume for this position, please complete the accommodation request form here.

Lilly does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, disability, or any other legally protected status.

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