IT Management & Business Others Marketing and PR Medical and Healthcare Other Science and Tech
1 - 3 Years
October 18, 2019
Clinical Trial Coordinator
Clinical Trial Coordinator
In this role, you have the opportunity to
join a fast-growing Philips venture, with the ability to disrupt a billion dollar industry and touch millions of lives by developing a unique medical device solution. Your challenge will be to support the European sales organization with a focus on the Netherlands, in a challenging phase of aggressive growth. This role offers the unique opportunity to be an entrepreneur and be part of this journey.
You are responsible for
Assisting with operational execution of clinical research involving human subjects from inception to close out
Assisting with ensuring all internal and external collaborating staff are appropriately organized, trained and managed to execute the research project
Preparing work abiding by applicable Regulatory statuses and withstanding scrutiny in the event of an audit
Overseeing preparation, shipping, accounting and archiving of all study-related materials
Interpreting assignments and performs appropriate analysis on own
Identifying key issues and patters from partial conflicting data
You are a part of
Philips EPD Solutions, a recently acquired venture with ambitious plans for growth, developing a disruptive technology, which will improve the efficiency and efficacy of life-saving cardiac ablation procedures treating among others atrial fibrillation. EPDs technology has the potential to address the key unmet need of real-time therapy assessment, which is one of the more significant limitations of the current standard of care. We aim to help to improve outcomes for millions of people and help maintain the rapidly rising cost of managing the disease. Having obtained CE mark and 510k approval in 2018, we are launching our product in Europe and US and are seeking regulatory approvals around the world.
To succeed in this role, you should have the following skills and experience
At least 2 years experience in the preparation and execution of clinical trials (e.g. as a Clinical Research Associate)
Preferably Bachelors degree, in biological sciences or healthcare
Good command of written and spoken English language
Excellent verbal and written communications skills
Excellent interpersonal and organizational skills
A pro-active, committed and motivated attitude
Preferably demonstrated working knowledge of GCP, ICH guidelines, FDA/EU regulations
Ability to work very accurate and thorough
Excellent record-keeping skills; good documentation practice
Ability to maintain excellent working relationships with a broad range of trial staff.
Ability to work well in a team environment but also independently without significant oversight
Ability to efficiently organize and prioritize work within a multifaceted framework and set deadlines.
Flexibility in work hours and readiness to travel.
In return, we offer you
A path towards your most rewarding career. Philips is growing its marketing capability enterprise wide. Succeeding in this market-based role in a complex environment will open many doors for your long term career, in other areas in Philips or otherwise. We also believe that we are at our best as a company when you are at yours as a person. Thus, we offer competitive health benefits, a flexible work schedule and access to local well-being focused activities.
Why should you join Philips?
Working at Philips is more than a job. Its a calling to create a healthier society through meaningful work, focused on improving 3 billion lives a year by delivering innovative solutions across the health continuum. Our people experience a variety of unexpected moments when their lives and careers come together in meaningful ways. Learn more by watching this video.
To find out more about what its like working for Philips at a personal level, visit the Working at Philips page on our career website, where you can read stories from our employee blog. Once there,you can also learn about our recruitment process, or find answers to some of the frequently asked questions.
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