6 дней назад
Associate Decentralized Clinical Trial Study Lead (aDCTL) / Decentralized Clinical Trial Lead (DCTL) (Clinical Trials)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Decentralized Clinical Trial Study Lead / Decentralized Clinical Trial Lead (Clinical Trials): Leading the strategic delivery of decentralized and hybrid clinical trials with an accent on project governance, customer engagement, cross-functional collaboration, and financial control. Focus on managing study risks and quality, coordinating technology and site-support stakeholders, and accelerating milestones while protecting scope and profitability.
Location: Sofia, Bulgaria
Company
IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Lead the strategic development and operational delivery of fully decentralized and hybrid clinical trial studies.
- Own customer relationships, provide project oversight, and communicate progress, risks, issues, and milestones to internal and external stakeholders.
- Set objectives for DCT project teams, assess performance, provide feedback, and support staff development.
- Collaborate with technology and IT, mobile nursing, site support services, regulatory, site start-up, and core study teams.
- Manage study quality, risks, contingencies, corrective and preventive actions, scope changes, and customer approvals.
- Control project budgets, resources, forecasts, profitability, and financial performance through study closeout.
Requirements
- Bachelor's degree in life sciences or a related field.
- At least 4 years of relevant clinical research experience and approximately 3 years of project management experience.
- Previous experience with electronic data capture, clinical trial CRFs, and/or data management.
- Advanced knowledge of project management methodologies, preferably in clinical research.
- Knowledge of clinical trial conduct, ICH GCP, and applicable local laws, regulations, and guidelines.
- Good command of English, with strong written, verbal, presentation, negotiation, and customer management skills.
Nice to have
- Experience setting up or implementing new platforms and systems.
- Experience preparing or leading bid defense presentations for virtual or hybrid DCT studies.
- Experience mentoring project team members and educating teams or partners on DCT processes and capabilities.
Culture & Benefits
- Work across multiple clinical trial delivery and healthcare functions.
- Follow established SOPs, policies, study tools, training materials, and quality processes.
- Contribute to continuous improvement by sharing lessons learned and best practices.
- Participate in corporate initiatives, change advocacy, and program-level executive committees when applicable.
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