Senior Clinical Research Associate

hace 4 semanas


Barcelona, España Worldwide Clinical Trials A tiempo completo

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

What Clinical Operations does at Worldwide

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.

Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.

What you will do

Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits

Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data

Actively participate in study team and investigator meetings

Compile and ensure completeness of regulatory documents and ethical submission documentation

What you will bring to the role

Excellent interpersonal, oral, and written communication skills in English and local language

Superior organizational skills with attention to detail, and the ability to work independently

Broad understanding of clinical research principles and process

Proficiency in Microsoft Office, CTMS, and EDC Systems

Your experience

At least two years of independent clinical monitoring experience

Demonstrable experience of handling multiple protocols across a range of therapeutic indications

Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree)

Ability to meet the travel requirements of the job

We love knowing that someone is going to have a better life because of the work we do.

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