Specialist, Site Contracts - Taiwan - Remote

WhattheSite Contractdepartmentdoes at Worldwide

Site Contracting is an essential function within any CRO, and our seasoned team spans decades of experience within the industry andpossessesrobust legal experience as well. The departmentis responsible forreviewing, analyzing, and drafting clinical research site contracts, investigatorcontractsand other project-related contracts. Our global team is familiar with the specific laws for the countries and sites we occupy. We negotiate andfinalizeclinical trial contracts and services contracts with the Worldwide Legal Department, study teams, Sponsors, investigators, and/or clinical sites.

What you will do

• Prepare country contract templates;

• Draft and send Site Agreements or any contracts associated to sites to begin negotiations;

• Negotiate contract(s) language and budget(s) with each assigned site to finalization / execution;

• Reviewstudy budgets and costspertaining tocontract negotiation;

• Perform quality check of Site Agreements or any documents associated before signature process starts;

• Liaisewith Worldwide Legal Department, Data Privacy team, study teams, Sponsor, sites, investigators etc.

• Send Fully Executed Site Agreements or any document associatedto:site, eTMF, payment team, Sponsor, post to internalSharepoint, as applicable;

• Negotiate Site Agreements Amendment language and budget with sites;

• Create termination letter or any other type of documents related, and send to sites for signature, as applicable;

• Maintain tracking tool with live/real-time/regular updates for functional activities;

What you will bring to the role

• Proficient in negotiating contract terms with clinical sites and vendors.

• Ability toidentifyand address contract issues and disputes efficiently.

• Good understanding of international and local regulatory requirements for clinical trials (e.g., FDA, EMA, ICH-GCP).

• Excellent verbal and written communication skills for effective interaction with internal stakeholders and clinical sites.

• Solid analytical skills to review and interpret contract terms andfinancialdata.

• Ability toidentifyrisks and develop mitigation strategies.

Your experience

• Bachelor's Degree or equivalent in business administration, finance,scienceor related field.

• 1 to 3 years of experience in Clinical Research Pharmaceutical or CRO industry working with investigator/site contracts or related legal field.

• Excellent verbal and written Englishand locallanguageskills.

• Proficiencywith MS Word,Exceland Outlook.