Senior Clinical Research Associate - CNS/Oncology - West Coast

Worldwide Clinical Trials•Virtual United States Arizona, AZ

3d•Remote

About The Position

Worldwide Clinical Trials is a global, midsize CRO that is dedicated to changing the way the world experiences CROs by taking pioneering, creative approaches to cure the world's most persistent diseases. Our mission is to work with passion and purpose every day to improve lives. We are looking for individuals who value this pursuit and want to make a difference for patients and their caregivers. We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity, and we are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Within Clinical Operations, the Clinical Research Associate (CRA) role offers a rewarding journey where contributions profoundly impact patients' lives. CRAs work alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues is ingrained in our culture. We offer extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. Professional development is a top priority, with regular touchpoints and coaching conversations with your Line Manager. We offer a clear career path and development that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and overcoming obstacles to improve patients' lives. This role offers an unparalleled experience to drive scientific breakthroughs and be at the core of every successful clinical trial.

Requirements

Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to detail
Ability to work with little or no supervision
Proficiency in Microsoft Office, CTMS, and EDC Systems
5+ years of experience as a Clinical Research Associate
4-year university degree OR Nursing Degree
Experience in CNS/Neurology and Oncology are required
Candidates must reside on the West Coast
Willingness to travel regionally required

Responsibilities

Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects.
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort.
Performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets.
Training the sites to collect data properly and report any potential safety-related events.
Managing the site's activities during study maintenance.
Closing down research activities at the sites once the study has concluded.
Conduct study initiation visits (SIVs).
Ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements, while most site management efforts will be performed remotely.

Benefits

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.
We offer 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.
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.