Senior Clinical Operations Lead Global Oncology Trials

Iqvia Argentina; Viseu; Presencial; EUR 70 000 - 90 000; Tempo integral

Resumo da oferta

IQVIA is seeking a Clinical Operations Lead to support the Clinical Trial Operational team in overseeing trials and coordinating with CROs and vendors. The role focuses on timeline management, site coordination, and strategic development of trial materials and IP plans.

The ideal candidate has at least 3 years in biopharma or clinical research, with 1 year in clinical project management and solid oncology knowledge.

Qualificações

• Minimum of 3 years' experience in the biopharmaceutical industry or other relevant clinical research experience.
• Minimum 1 year or experience in Clinical Project Management.
• Proven work experience and knowledge of Oncology therapeutic area.
• Bachelor's Degree or relevant degree with strong emphasis on Science.
• Prior experience in assisting the conduct and management of multinational/ global clinical trials.
• Strong experience in vendor management.
• Working knowledge of ICH Good Clinical Practices and other relevant regulatory experience.
• Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously.
• Strong communication skills with internal teams, sites, and vendors.

Responsabilidades

• Assist in the review, development and writing of clinical trial documents and manuals, including study manuals, laboratory or biomarker plans.
• Create Master ICF template and review site changes. Update template for new risks and new amendments information.
• Participate in the feasibility and evaluation of investigative sites.
• Assist in the development and management of study timelines and priorities, including recruitment tools/ strategy and patient retentions plan.
• Plan and organize meetings with team support (eg. investigator/ coordinator meetings).
• Assist in the development of the IP and co-medication strategy.
• Monitor study specific timelines and key deliverables; focus on management of vendors (eg. Monitoring, Sample management, IVRS, Laboratory).
• Develop relationships with investigational sites and institutions to enhance conduct of the trial.
• Acts as preliminary liaison for study sites to convey trial information, answer questions and in accordance with the escalation pathway.

Descrição da oferta de emprego

IQVIA is seeking a Clinical Operations Lead to support the Clinical Trial Operational team in overseeing trials and coordinating with CROs and vendors. The role focuses on timeline management, site coordination, and strategic development of trial materials and IP plans.

The ideal candidate has at least 3 years in biopharma or clinical research, with 1 year in clinical project management and solid oncology knowledge.