Senior Project Manager

Kapadi; Madrid; Presencial; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A clinical research organization is seeking a highly-motivated Senior Project Manager to oversee interdisciplinary clinical research studies in oncology. You'll manage project performance, act as the liaison with clients, and lead a project team to ensure quality and compliance with regulatory standards. Ideal candidates will have extensive experience in clinical R&D, particularly in oncology. This role offers an opportunity to contribute to life-changing therapies for cancer patients.

Formación

• Minimum of 5 years of experience in clinical R&D.
• At least 2 years of experience in a CRO providing clinical research services.
• 5 years of oncology clinical or research experience preferred.

Responsabilidades

• Manage project overseeing clinical research studies.
• Act as liaison between the company and the customer.
• Lead project team, ensuring quality and performance.

Conocimientos

Clinical research knowledge

Oncology knowledge

Team leadership

Good Clinical Practice knowledge

Educación

Bachelor’s Degree in Life Sciences, Medicine, Pharmacy, 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.
• Act as a primary liaison between the company and the customer to ensure timely study initiation, conduct, and closeout according to the customer’s and the company’s contractual agreement, ensuring satisfaction levels are met and statuses of deliverables are communicated effectively.
• 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.
• Coordinate activities and deliverables of all study conduct partners and proactively identify and manage issues.
• 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.
• Routinely review clinical systems, dashboards, and documentation (e.g., Site Assessment Reports) to oversee site and study team conduct and identify any risks to delivery or quality.
• Possibly participate in customer proposal development and bid defenses.

Knowledge, skills and abilities :

• Demonstrated knowledge of the clinical research and development process in pharmaceutical and / or biotechnology industries.
• Demonstrated knowledge of oncology therapeutic area.
• Demonstrated ability to lead multidisciplinary teams of professionals, including vendor management.
• Strong knowledge of Good Clinical Practice / ICH guidelines and other applicable regulatory requirements.

Requirements :

• 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., oversight of CRAs).
• 5 years of oncology clinical or research experience preferred. Immuno-oncology and cell therapy experience also required.