Trial Capabilities Associate (계약직) at Lilly

Kyiv, , Ukraine -

Full Time

Start Date

Immediate

Expiry Date

24 Jan, 26

Salary

0.0

Posted On

26 Oct, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Documents, Informed Consent, Budget Negotiation, Contract Management, Site Compliance, Clinical Trial Management, Financial Transactions, Issue Resolution, Clinical Trial Material, Translation Process, Trial Master Files, Inspection Readiness

Industry

Pharmaceutical Manufacturing

Description

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. Initiate investigator site activities, including collection and submission of regulatory documents, customization and negotiation of informed consent documents, serve as the point of contact for a site’s ERB and Competent Authority (CA)(where applicable), communicate and negotiate budgets with site personnel and internal teams, negotiate and obtain fully-executed contract, track and ensure site compliance to required training, and effectively drive timelines aligned with company priorities Communicate with sites to enable start-up and maintain an active collaboration with sites during maintenance and close-out Communicate with various internal and external party / clinical research organization to enable active collaboration during site activation, maintenance and close-out Site budget/contract development and management Manage investigator payments and any other financial transactions Identify, communicate, and resolve issues Coordinate the management and delivery of clinical trial material Coordinate translation process for clinical trial documents and oversight of translation quality Populate internal systems to ensure accuracy of trial / site performance Populate Trial Master Files and libraries for future reference Inspection readiness of regulatory documents and processes 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. #WeAreLilly

Responsibilities

The Trial Capabilities Associate will initiate investigator site activities and maintain collaboration with sites during the trial process. Responsibilities include managing budgets, contracts, and compliance, as well as coordinating clinical trial materials and translations.