Senior Clinical Research Associate - CNS / Oncology - Spain - Remote

Worldwide Clinical Trials; Málaga; A distancia; EUR 50.000 - 70.000; Jornada completa

Descripción de la vacante

A global CRO is seeking a Senior Clinical Research Associate to join their dynamic team in Málaga. The role focuses on diverse therapeutic areas, requiring excellent communication and organizational skills, with a strong emphasis on independent monitoring. Ideal candidates will possess a life sciences background and considerable clinical trial experience, contributing significantly to impactful research initiatives. Join a company that values innovation and inclusiveness, and take your career further in clinical operations.

Formación

• At least two years independent clinical monitoring experience.
• Ability to handle multiple protocols across a range of therapeutic indications.
• Comprehensive understanding of clinical research principles and processes.

Responsabilidades

• Conduct site qualifications, initiation, interim monitoring, and close-out visits.
• Ensure regulatory documents and ethical submissions are complete.
• Review study subject safety information and informed consent compliance.

Conocimientos

Interpersonal Skills

Communication Skills

Organizational Skills

Attention to Detail

Educación

Four-year college curriculum in life sciences

Two-year college curriculum or equivalent

Herramientas

Microsoft Office

CTMS

EDC Systems

Descripción del empleo

Senior Clinical Research Associate - CNS / Oncology - Spain - Remote Senior Clinical Research Associate - CNS / Oncology - Spain - Remote

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.

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.

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 Does At Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.

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.

We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!

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 and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)

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, 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 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.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law . Seniority level

• Seniority level Mid-Senior level

Employment type

• Employment type Full-time

Job function

• Job function Research, Analyst, and Information Technology
• Industries Research Services

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