Senior Clinical Research Associate - Spain - Home-basedJoin to apply for the Senior Clinical Research Associate - Spain - Home-based role at Worldwide Clinical TrialsContinue with Google Continue with GoogleSenior Clinical Research Associate - Spain - Home-based2 days ago Be among the first 25 applicantsJoin to apply for the Senior Clinical Research Associate - Spain - Home-based role at Worldwide Clinical TrialsWho We AreWe’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 AreWe’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 WorldwideWe 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 WorldwideAt 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 DoConduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visitsReview study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of dataActively participate in study team and investigator meetingsCompile 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 RoleExcellent interpersonal, oral, and written communication skills in English and local languageSuperior organizational skills with attention to details, and the ability to work independentlyBroad understanding of clinical research principles and processProficiency in Microsoft Office, CTMS and EDC SystemsYour ExperienceAt least two years independent clinical monitoring experienceDemonstrable experience of handling multiple protocols across a range of therapeutic indicationsFour-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 jobWe 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 levelSeniority levelMid-Senior levelEmployment typeEmployment typeFull-timeJob functionJob functionResearch, Analyst, and Information TechnologyResearch ServicesReferrals increase your chances of interviewing at Worldwide Clinical Trials by 2xGet notified about new Senior Clinical Research Associate jobs in Madrid, Community of Madrid, Spain .Tres Cantos, Community of Madrid, Spain 2 weeks agoClinical Trial Manager - Spain - Neuroscience / Ophthalmology / Infectious DiseaseMadrid, Community of Madrid, Spain 2 weeks agoMadrid, Community of Madrid, Spain 6 days agoClinical Trial Strategy and Operations ManagerGreater Madrid Metropolitan Area 1 day agoClinical Project Manager / Senior Clinical Project ManagerClinical Project Manager / Senior Clinical Project ManagerMadrid, Community of Madrid, Spain 4 weeks agoMadrid, Community of Madrid, Spain 6 days agoMadrid, Community of Madrid, Spain 6 days agoAssociate Clinical Trial Manager (PhD) - Neuroscience / OphthalmologyMadrid, Community of Madrid, Spain 2 weeks agoAssociate Clinical Trial Manager (PhD) - Infectious Disease / ImmunologyMadrid, Community of Madrid, Spain 1 day agoResearch Manager, Third-Party Due DiligenceMadrid, Community of Madrid, Spain 1 week agoMadrid, Community of Madrid, Spain 12 hours agoSenior Manager Regional Site Engagement Management (RSEM) (m / f / x) SpainLead, Trial Delivery Manager, Oncology (5 Openings)Madrid, Community of Madrid, Spain 2 days agoMadrid, Community of Madrid, Spain 2 weeks agoLead, Trial Delivery Manager, Oncology (5 Openings)Madrid, Community of Madrid, Spain 2 days agoManager, Clinical Monitoring (English and French speaking)Manager, Clinical Monitoring (English and French speaking)Manager I - Study Startup and MaintenanceGlobal Senior Trial Delivery Manager - Sponsor DedicatedMadrid, Community of Madrid, Spain 1 week agoMadrid, Community of Madrid, Spain 20 hours agoMadrid, Community of Madrid, Spain 16 hours agoMadrid, Community of Madrid, Spain 6 days agoMadrid, Community of Madrid, Spain 3 weeks agoClinical Research Associate II / Sr. CRA, SpainWe’re unlocking community knowledge in a new way. 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