Real-World Evidence
Hybrid/Home based from different countries in EMEA.
Join us on our exciting journey!
IQVIA Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients.
Our approach is unique in the industry and is defining the way companies develop and apply real-world evidence for healthcare decision making.
We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of real-world evidence in an evolving industry.
Due to continued growth, we are seeking new brave minds to join our award winning and innovative department.
Essential Functions
- Contracts negotiation with Sites based in France (good knowledge of the "convention unique" is needed).
- Ensure adherence to good clinical practice (GCP), standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables, and to project timelines.
- Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
- Prepare site regulatory documents, reviewing for completeness and accuracy.
- Review, prepare and negotiate site contracts and budgets with sites, where applicable.
- Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
- Review and provide feedback to management on site performance metrics.
- Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
- Inform team members of completion of regulatory and contractual documents for individual sites.
- Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory /ethics submissions and ICF adaptation and negotiation, in line with project timelines.
- Provide local expertise to Clinical Operations Lead and Project team during initial and on-going project timelines planning.
- Perform quality control of documents provided by sites.
- May have direct contact with sponsors on specific initiatives.
- May perform Site Selection Visits if a trained monitor.
- May participate in feasibility and/or site identification activities.
- Degree in scientific discipline or health care preferred.
- Minimum of 3 years clinical experience required.
- Equivalent combination of education, training and experience may be acceptable.
- Knowledge of clinical research process and medical terminology.
- Good written and verbal communication skills including good command of English and French language.
- Good organizational and problem-solving skills.
- Ability to manage multiple priorities within various clinical trials.
- Ability to reason independently to assess and recommend specific solutions in clinical settings.
- Ability to establish and maintain effective working relationships with coworkers, managers and clients.
- Ability to understand electronic data capture including basic data processing functions.
- Familiarity with current International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines and applicable regulations to the conduct of clinical research.
- Ability to mentor other employees.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
