Senior Clinical Research Associate - Madrid, España - Worldwide Clinical Trials

Worldwide Clinical Trials

Empresa verificada

Madrid, España

hace 2 semanas

Publicado por:

Isabel García

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Descripción

Requisition Number

7313

Employment Type:

Regular

Who we are

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality.

Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers.

From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed.

We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.

We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Join us

What Clinical Operations Site Management does at Worldwide

Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial.

All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience - one you can't get anywhere else, with a team unlike anyone else.

What you will do

Conduct all types of visits site qualifications, initiation, interim monitoring, site management and study closeout visits
Actively participate in study team and investigator meetings

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 details
Broad understanding of clinical research principles and process
Proficiency in Microsoft Office, CTMS and EDC Systems

Your background

Fouryear college curriculum in life sciences, OR
Twoyear college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and one year experience with clinical research (e.g. study coordinator, CTA, etc.)
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.