Clinical Trial Manager

hace 4 semanas


Madrid, Madrid, España Medpace A tiempo completo
Job Summary:

Medpace, a leading CRO for Biotech companies, is seeking a Clinical Trial Manager to join our Clinical Trial Management Group in Spain. The ideal candidate will have expertise in Neuroscience and CNS, with the ability to manage day-to-day operations of clinical trials and provide cross-functional oversight of internal project team members.

As a Clinical Trial Manager, you will be responsible for managing and providing accountability for project operations, serving as the primary Sponsor contact for operational project-specific issues, and maintaining in-depth knowledge of protocol, therapeutic area, and indication.

We offer a competitive salary/bonus program, plus equity grants, and provide remote flexibility for experienced candidates.



Responsibilities:


Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations.

Serve as primary Sponsor contact for operational project-specific issues and study deliverables.

Maintain in-depth knowledge of protocol, therapeutic area, and indication.

Provide cross-functional oversight of internal project team members and deliverables.

Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable.

Develop operational project plans.

Manage risk assessment and execution.

Responsible for management of study vendor.

Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.



Qualifications:
Bachelor's degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred.

Experience in Phases 1-4; Phases 2-3 preferred.

Minimum of 2 years of Clinical Trial Management experience; CRO experience preferred.

5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role.

Management of overall project timeline; Bid defense experience preferred.

Strong leadership skills.



Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.

We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace? People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.

The work we do today will improve the lives of people living with illness and disease in the future.


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