Lilly
 

Career Opportunities

 
Job Posting Number
Job Description
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1

CLINICAL RESEARCH NURSE – (CRN)

JOB DESCRIPTION:

  • Participates in the review of draft protocols.
  • Participates in recruitment activities via approved media, flyers and brochures. Identify and source for appropriate sites or avenues for subject recruitment.
  • Conducts and coordinates all general screening activities such as screening laboratory tests, clinical procedures and data documentation.
  • Ensures that recruitment/screening activities are in compliance with ICH-GCP (Good Clinical Practice), global and local SOP and guidelines, Singapore GCP and regulatory requirements.
  • Responsible for organising and managing the protocol set-up activities which involves the development of appropriate forms, labels, set-up medical equipment and arranging pre-study meetings.
  • Participates in clinical trial procedure/tasks as delegated by the Principal Investigator or designee.
  • Collects and verifies clinical trial data.
  • Demonstrates understanding and adheres to Good Clinical Practice, global and local policies and procedures and relevant regulatory requirements.

REQUIREMENTS:

  • Registered with Singapore Nursing Board.
  • Strong communication and customer relation skills.
  • Pleasant disposition, meticulous and systematic.
  • Able to multi-task and perform under pressure of strict timelines.
  • Computer literate.

We regret that only shortlisted candidates will be notified.

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2

LABORATORY SYSTEMS ASSOCIATE

JOB DESCRIPTION:

  • Establishes, develops, executes and completes installation records, qualification protocols and validation documentation.
  • Performs direct installation activities, such as creation, execution and completion of installation records.
  • Performs direct qualification activities, such as creation, execution and completion of qualification protocol (QMP, DQ/UR, IO, OQ, PQ and QSR).
  • Performs direct validation activities, such as creation, execution and completion of validation documentation (Validation plan, System Overview, Design Specifications, requirements, traceability matrix, Test Plan, Test cases, validation report, etc.) and supporting documents (i.e. Data Flow Diagrams).
  • Conducts validation or qualification tests of new or existing processes, equipment, or software, in accordance with internal protocols and where applicable, external standards.
  • Conducts routine review of validation or qualification documentation and processes to ensure compliance with internal or regulatory requirements.
  • Liaises with external parties on equipment and consumables.
  • Utilises various software applications, such as spreadsheet, relational databases, and electronic mail, to assemble or format data or test reports.
  • Performs entry and verification of data in laboratory systems and equipment.
  • Familiar with CSQ policies, procedures, SOPs and regulatory requirements for laboratory systems and equipment.
  • Tracks equipment issues/problems via an appropriate change control and problem management system.
  • Tracks equipment/system changes including but not limited to configuration change, access review or documentation update via an appropriate change and problem management system.

REQUIREMENTS:

  • Diploma or Degree in Life Sciences, Engineering, Information Systems or Computer Systems.
  • Preferable with biomedical and/or clinical research experience.
  • Good communication, time management and interpersonal skills.
  • Flexibility in work outlook.

We regret that only shortlisted candidates will be notified.

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3

PHARMACIST

JOB DESCRIPTION:

  • Ensures proper investigational product (IP) management which includes sourcing, receipt, storage, preparation, dispensing, labelling, inventory accountability, reconciliation, retention, destruction and documentation according to the study protocol.
  • Ensures proper management of non-study medications, e-kit drugs and other general pharmacy inventory.
  • Ensures proper management of Special Security Substances (SSS), Controlled Drugs and Psychotropic drugs.
  • Performs extemporaneous preparation (EP), aseptic compounding and other dispensing activities in accordance to operational procedures, manuals, preparation instructions and various quality agreements.
  • Ensures proper management of randomization and unblinding procedures for blinded clinical trials.
  • Assists Clinical Research Technologists (CRT) in maintaining proper functioning of all pharmacy equipment.
  • Reviews and provides feedback during protocol development where applicable.
  • Reviews and updates Pharmacy local standard operation procedures as appropriate.
  • Participates in applicable audit and inspection visits by Lilly and external agencies and ensures follow-up to issues takes place.
  • May require to hold relevant licenses (e.g. Form A license for poisons and psychotropic import license).
  • Provides coaching to Locum Pharmacists and Pharmacy Technicians/Assistants as needed on IP management and aseptic compounding.

REQUIREMENTS:

  • Singapore Registered Pharmacist.
  • Previous Hospital Pharmacy Experience (preferred).
  • Able to work in cleanroom environment which requires special gowning procedure.
  • Experience in working in cleanroom or manufacturing setting (preferred).
  • General GMP and GDP knowledge (preferred).
  • Must be flexible with work hours to participate in study activities which occur predominantly in the early morning.

We regret that only shortlisted candidates will be notified.

Apply Online