Sr Project Manager - Medical Devices

Avania; España; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A medical devices company is seeking a Senior Project Manager to oversee clinical trial activities from start to close. The ideal candidate will have over 7 years of experience in clinical trials, project management skills, and a relevant degree. This role offers a competitive compensation package and the possibility of hybrid or fully remote work opportunities.

Servicios

Competitive compensation and benefits package

Training and development opportunities

Flexible working arrangements

Formación

• GCP-ICH-E6, FDA regulations and ISO knowledge.
• 7+ years’ experience in clinical trials, including 1 year as a Sr. CRA.
• Fluent in spoken and written English.

Responsabilidades

• Supervise the Project Team to ensure trial deliverables are on time.
• Manage project planning and tracking of trial progress.
• Maintain budget reviews for allocated studies.

Conocimientos

Project management

Budget management

Communication

Regulatory knowledge

Educación

Relevant degree in (para)medical life science or nursing

Herramientas

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Descripción del empleo

Overview

Avania are hiring - Senior Project Manager - Medical Devices

As the Sr Project Manager, you will have the opportunity to provide leadership through planning, organizing and overseeing all clinical trial activities and deliverables from study start-up to close out.

The Senior Project Manager is responsible for the scope, schedule, budget and quality of multi site, multi service complex clinical trials involving; implementing and managing the project planning; tracking of the clinical monitoring process; administration and overview of clinical trials. The position requires a proactive approach in developing the project planning and monitoring of both resources and clinical trial so that all aspects of the plan can progress effectively.

Responsibilities

• Supervise the Project Team to ensure trial deliverables are on time, within budget and in appropriate quality, in compliance with applicable SOPs, ISO14155 / ICH-GCP and all applicable (local) regulations
• Manage the project planning and tracking of trial progress of various international clinical trials from start-up to close out
• Maintain and perform regular budget reviews for your allocated studies
• Assist the Management Team in preparing budgets and forecasts as required and possibly have involvement in bid defense meetings
• Keep our quality standards high for our clients

Qualifications

• Relevant degree in (para)medical life science or nursing preferred
• GCP-ICH-E6, FDA regulations and ISO 14155,13485 and 9001 knowledge where applicable
• Knowledge of regulatory regulations and guidelines on medical devices
• Prior PM experience of multi site, multi service complex clinical trials with a strong finance / budget management skill set
• Experience within Medical Device / MedTech with a focus on cardiovascular therapeutics
• 7+ years’ experience in clinical trials with at least 1 year as a Sr. CRA preferred
• Ability to travel domestically and internationally
• Proficient in the use of computer and software systems (Microsoft Word, Excel, PowerPoint, email)
• Fluent in spoken and written English, with excellent communications and interpersonal skills

We offer

• The opportunity to work in an innovative, fast-growing and rewarding industry
• A dynamic and enthusiastic global team that fosters collaboration and the opportunity to work with experts across many specialties
• Exchange of knowledge and ideas to help employees grow and advance their careers, backed with training and other development opportunities
• Competitive compensation and benefits package (details shared during the interview process)
• Some roles offer the opportunities for travel
• Ask us about our hybrid and fully remote work opportunities

We look forward to receiving your application!

When you need to advance your career, it takes Avania!