IQVIA Biotech
Biotech
SeniorSiteContractAssociate
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optimal for Senior candidates.
“Senior Site Contract Associate at IQVIA Biotech. Skills: Site contracting, Contract negotiation, Clinical trials. Support delivery of start-up contracting activities. Develop investigator grant estimates”
Industry & Context.
What They're Looking For.
Must Have
Bachelor's Degree in life sciences or health care, 5-7 years relevant experience, Demonstrable experience acting as a contract negotiator, Relevant sponsor or clinical research organization clinical site contracting experience, Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards, Knowledge of Microsoft Office and e-mail applications
Nice to Have
Understanding of regulated clinical trial environment, Knowledge of drug development process, Ability to interpret pricing models, Ability to prepare proposals, bid grids and budgets
What You'll Do.
Support delivery of start-up contracting activities
Develop investigator grant estimates
Develop proposal text
Utilize contract and budget templates
Maintain contracting systems
Ensure collaboration with sponsors and stakeholders
Deliver project scope in compliance with sponsor requirements
Provide operational and financial contracting support
Facilitate business development and initiation of clinical trials
Enable compliance with regulatory requirements
Assist in creation of scientific documentation
Assist in review of technical documentation
Assist in review of administrative documentation
Contribute to collection of contracting intelligence
Contribute to interpretation of contracting intelligence
Contribute to analysis of contracting intelligence
Contribute to dissemination of contracting intelligence
Ensure contracting efficiency
Ensure adherence to project timelines
Report contracting performance metrics
Report out of scope contracting activities
Comply with contract management standards
Comply with quality standards
Provide administrative support to analysts
Provide operational support to analysts
Ensure accurate completion of internal systems
Ensure accurate maintenance of internal systems
Ensure accurate completion of databases
Ensure accurate maintenance of databases
Ensure accurate completion of tracking tools
Ensure accurate maintenance of tracking tools
Ensure accurate completion of project plans
Ensure accurate maintenance of project plans
How You'll Work.
Team & Collaboration
Communication with sponsors; Communication with stakeholders; Communication with RSU regions; Communication with countries; Working relationships with co-workers; Working relationships with managers; Working relationships with sponsors
Communication Scope
Communication skills
Process & Methodology
Project Plan
Full Job Description
**Site Contracts Analyst** **IQVIA Biotech** **Bulgaria, Serbia, Spain, Slovakia - Homebased** IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster. **Job Overview** Support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsor’s requirements, including pre-award activities. **Essential Functions** * Develop simple investigator grant estimates and proposal text to support the proposal development process. * Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy. * Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan. * Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. * Assist in the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required. * Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required. * Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting perfo
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