Sr. Associate / Manager - Clinical Information Systems (IRT) at Eli Lilly and Company

Cork, County Cork, Ireland

Eli Lilly and Company Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, HealthcareIndustries

Requirements

  • Strong collaboration skills with clinical study teams and key functions
  • Deep understanding of system functionalities, capabilities, and limitations for Lilly’s internal IRT/IWRS
  • Expertise in the Study Development Process to review protocol requirements and establish timelines
  • Ability to provide validated study-specific IRT/IWRS builds meeting approved customer requirements
  • Proficiency in maintaining confidentiality and blinding
  • Strong knowledge of the System Development Cycle, including study-specific system requirements
  • Experience executing study set-up from requirements approval through implementation
  • Capability to create study-specific documents, including clinical-trial site IRT/IWRS user tools
  • Ability to ensure timelines are met according to agreed-upon system-need dates
  • Commitment to sustaining a culture of quality and compliance
  • Proactive mindset for improving day-to-day activities and communicating opportunities
  • Willingness to participate in/support local/divisional projects and process improvement initiatives

Responsibilities

  • Build and maintain effective business partnerships with clinical study teams and key functions
  • Participate in Study Development Process to review study-specific protocol requirements and establish implementation timelines
  • Provide a validated study-specific IRT/IWRS build that meets approved customer requirements
  • Ensure confidentiality and blinding is appropriately maintained at all times
  • Participate in all aspects of the System Development Cycle, including executing the study set-up process from requirements approval through implementation
  • Create study-specific documents including clinical-trial site IRT/IWRS user tools
  • Ensure timelines are met according to agreed-upon system-need dates
  • Sustain a culture of quality and compliance
  • Proactively identify ways to improve day-to-day activities and practices, and actively communicate opportunities to peers and leadership team
  • Participate in and/or support the implementation of local/divisional projects and other process improvement initiatives

Skills

Key technologies and capabilities for this role

Clinical Information SystemsIRTClinical TrialsHealthcare ITInformation Technology

Questions & Answers

Common questions about this position

What benefits does Eli Lilly Cork offer?

Eli Lilly Cork offers flexible hybrid working options, healthcare, pension and life assurance benefits, subsidised canteen, onsite gym, travel subsidies, on-site parking, inhouse People Development services, Educational Assistance, and ‘Live Your BEST Life’ wellbeing initiatives.

Is this a remote or hybrid role?

The role offers flexible hybrid working options from the campus in Little Island, Cork.

What key responsibilities are involved in this role?

Key responsibilities include consultation, study set-up and execution, building effective business partnerships with clinical study teams, understanding system functionalities for Lilly’s internal IRT/IWRS, and participating in Study Development.

What is the company culture like at Eli Lilly Cork?

Eli Lilly Cork features a talented diverse team of over 2000 employees across 60 nationalities, emphasizes putting people first, and is committed to diversity, equity, and inclusion with pillars like EnAble, embRACE, LGBTQ+ & Ally, and GIN-Gender Inclusion Network.

What qualities make a strong candidate for this position?

A strong candidate is customer-focused, quality-centric, consistently exceeds expectations, thrives in a challenging and dynamic environment, and excels at building partnerships with clinical study teams.

Eli Lilly and Company

Develops and delivers prescription medicines globally

About Eli Lilly and Company

Eli Lilly and Company is a global pharmaceutical company that focuses on discovering, developing, and delivering medicines to improve health. The company has a long history of scientific achievements, including the creation of insulin, the first life-saving treatment for diabetes. Lilly's operations involve extensive research and development to create new medications and enhance existing ones, ensuring they are safe and effective. Their products are primarily prescription medicines sold to healthcare providers for various medical conditions, including diabetes, cancer, and pain management. What sets Lilly apart from its competitors is its strong commitment to ethical practices and the protection of its products from counterfeiting. The company's goal is to enhance lives through innovative medical solutions while maintaining high standards of quality and ethics.

Indianapolis, IndianaHeadquarters
1876Year Founded
$1,180.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Competition from Novo Nordisk's Ozempic may impact tirzepatide's market share.
Potential construction delays in Indiana could affect GLP-1 drug production timelines.
Regulatory challenges may hinder Kisunla's expansion in new Alzheimer's markets.

Differentiation

Eli Lilly's rich history includes the first life-saving insulin treatment.
Lilly's strategic partnerships enhance its position in neurodegenerative disease treatments.
FDA approval of Zepbound opens new therapeutic markets for sleep disorder treatments.

Upsides

Lilly's $9 billion complex in Indiana boosts GLP-1 drug production capacity.
Kisunla's approval in China expands Lilly's Alzheimer's treatment market in Asia.
Collaboration with EVA Pharma enhances Lilly's reputation as socially responsible.

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