Senior Clinical Research Associate - Spain - Remote

Senior Clinical Research Associate - Spain - Remote 1 day ago Be among the first 25 applicants

Overview We’re Worldwide Clinical Trials, a global midsize CRO with a team of over 3,500+ experts. Our mission is to work with passion and purpose every day to improve lives. We value pioneering, creative approaches and high-quality execution across diverse therapeutic areas.

We are committed to a diverse and inclusive environment that enables professionals from all backgrounds to succeed. We strive to enable collaboration, transparency, and opportunities for professional growth within a supportive team.

What Clinical Operations Does At Worldwide At Worldwide Clinical Trials, you will embark on a rewarding journey within Clinical Operations. In a CRA role, you will work with colleagues across therapeutic areas such as Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. You will receive support through regulatory submissions, TMF management, and collaboration with in-house CRAs for projects with heavy site management needs. Regular coaching and development discussions are in place to support a clear career path toward roles such as Clinical Trial Manager.

We offer an environment that values impactful scientific work and the chance to contribute to successful clinical trials globally.

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; conduct source document verification for compliance, patient safety, and data veracity

Actively participate in study team and investigator meetings

Compile and ensure completeness of regulatory documents and ethical submission documentation; review study subject safety information and informed consent and study materials (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 detail, and the ability to work independently

Broad understanding of clinical research principles and processes

Proficiency in Microsoft Office, CTMS, and EDC Systems

Your Experience At least two years of independent clinical monitoring experience

Demonstrable experience in 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.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, 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.

Employment and Seniority Seniority level : Mid-Senior level

Employment type : Full-time

Job function : Research, Analyst, and Information Technology

Industries : Research Services

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