Clinical Research Intern

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Intern – Investigator Engagement Assistant (Clinical Research)

Purpose:

The Intern – Investigator Engagement Assistant supports the Clinical Research Lead (CRL) and the Investigator Engagement organization in administrative and operational tasks related to clinical trials. This role is designed to provide learning opportunities and entry-level experience in the clinical phase of drug development.

Primary Responsibilities: This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

The following are key responsibilities

• Support office Management (logistics associated with office organisations, supplies)
• Administrative support for clinical trials as required
• Assist with document management – (eg: scan, upload, electronic Trial Master File maintenance activities)
• In-house administrative support for CRLs who are travelling (eg: confidentiality agreement creation/follow-up, archival of CV, Contract, Ethics committee decisions, invoices, budget forms, proformas)
• Support Investigator Engagement business systems and process as required
• Support of local printing and shipment of documents where necessary
• Support scanning financial documantation and following process
• Maintenance of collaboration sites
• Gain working knowledge of local regulatory agency and ethical review board processes
• Training and working within the boundaries of Good Clinical Practice requirements
• Working with Good Documentation Practices

SIP Support for Investigator Engagement in Turkey:

• Register site and users by contacting and supporting sites
• Follow up site profile and facility profile completion

Minimum Qualification Requirements:

• Currently enrolled in a relevant university program (e.g., Life Sciences, Pharmacy, Medicine, or related field).
• Knowledge of Good Documentation Practices
• Excellent computer skills with experience in a variety of software packages
• Fluency in English both written and oral.
• High level of attention to detail
• Strong self-management, communication and organizational skills

Other Information/Additional Preferences:

• Flexibility
• Excellent problem solving skills
• Ability to work in a virtual team and across cultures

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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

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