Senior Project Manager Data

Kapadi; Madrid; Presencial; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A full service CRO in Madrid is seeking a highly motivated Senior Project Manager to oversee interdisciplinary clinical research studies. The ideal candidate will have over 5 years of experience in clinical R&D and proven leadership skills. This role requires managing project timelines, financial performance, and ensuring compliance with risk management strategies.

Formación

• Minimum of 5 years experience in clinical R&D.
• At least 2 years experience in a CRO.
• Strong understanding of risk management strategies.

Responsabilidades

• Manage interdisciplinary clinical research studies.
• Lead project team and oversee quality of deliverables.
• Account for financial performance of assigned projects.

Conocimientos

Project management

Clinical research

Risk management

Team leadership

Educación

Bachelor’s Degree in Life Sciences, Medicine, Pharmacy, or Nursing

Descripción del empleo

Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated technology to provide higher quality and faster access to results. We are looking for a highly-motivated

Senior Project Manager

to help us continue to grow our business and deliver new, life-changing therapies for the cancer patients who need them.

As a Senior Project Manager, you will :

• Manage a project overseeing interdisciplinary clinical research studies.
• Lead a project team and oversee quality of clinical monitoring, timeline and site management deliverables.
• Be accountable for the financial performance of each assigned project.
• Review study and site data listings and visualizations via analytical dashboards and / or reports to identify trends, risks, and suspected scientific misconduct on other systematic errors that could impact data integrity and subject safety.
• Drive risk identification and risk monitoring strategy cross-functionally, ensuring that appropriate risk monitoring tactics are written into the CMP, and be accountable for the clinical team’s understanding, ongoing compliance and delivery according to the stated monitoring strategy, CMP, and risk plans.
• Create and maintain relevant project plans.
• Site Assessment Reports) to oversee site and study team conduct and identify any risks to delivery or quality.
• Demonstrated ability to lead multidisciplinary teams of professionals, including vendor management.
• Bachelor’s Degree (or equivalent) level of qualification in Life Sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience.
• Minimum of 5 years of experience in clinical R&D in pharmaceutical, biotechnology and / or clinical research organization (CRO) businesses, including at least 2 years of experience in a CRO providing clinical research services to pharmaceutical, biotechnology or medical device companies, and including at least 2 years of clinical management experience (i.e.,