Senior Clinical Research Associate - CNS/Oncology - West Coast
Worldwide Clinical Trials · Arizona, United States
- Hybrid
- Full-time
- $100,000 / year
- Arizona, United States
Job highlights
- Manage clinical research site activities and regulatory compliance.
- Engage in all study phases from site identification to close-out.
- Conduct study initiation visits and ensure data integrity.
- Require strong communication, organization, and self-supervision skills.
- Must have 5+ years CRA experience in CNS/Oncology.
About the role
About Worldwide Clinical Trials
We are 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. 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!
Clinical Operations 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
- 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, and closing down research activities at the sites once the study has concluded.
- Conduct study initiation visits (SIVs).
- While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements.
What You Will Bring To The Role
- 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.
Your Experience
- 5+ years of experience as a Clinical Research Associate.
- 4-year university degree OR Nursing Degree.
- Experience in CNS and Oncology are required.
- Candidates must reside on the West Coast.
- Willingness to travel regionally required.
Key skills/competency
- Clinical Research Associate
- CNS Oncology
- Clinical Operations
- Regulatory Submissions
- TMF Management
- Site Management
- Data Collection
- Safety Reporting
- Informed Consent
- Clinical Trials
Skills & topics
- Clinical Research Associate
- CRA
- CNS Oncology
- Clinical Operations
- Clinical Trials
- CRO
- Regulatory Submissions
- TMF Management
- Site Management
- Data Collection
- Safety Reporting
- Informed Consent
- Biotechnology
- Pharmaceutical
- Healthcare
- Life Sciences
How to get hired
- Tailor your resume: Highlight your 5+ years of CRA experience, specifically mentioning CNS and Oncology work. Quantify achievements where possible to demonstrate impact.
- Showcase relevant skills: Emphasize your expertise in regulatory submissions, TMF management, CTMS, and EDC systems, as well as your excellent interpersonal and organizational abilities.
- Address the location requirement: Clearly state that you reside on the West Coast to meet the geographic prerequisite for this Senior Clinical Research Associate role.
- Prepare for interviews: Be ready to discuss your experience in managing research sites remotely and in-person, your approach to data integrity, and your understanding of regulatory requirements in CNS and Oncology trials.
- Express passion for purpose: Align your application with Worldwide Clinical Trials' mission of improving lives and making a difference in patient care.
Technical preparation
Behavioral questions
Frequently asked questions
- What is the primary therapeutic focus for this Senior Clinical Research Associate role at Worldwide Clinical Trials?
- The primary therapeutic focus for this Senior Clinical Research Associate position is CNS (Central Nervous System) and Oncology. Candidates with specific experience in these areas are highly preferred.
- Does this Senior Clinical Research Associate job require travel?
- Yes, this Senior Clinical Research Associate role requires a willingness to travel regionally. While most site management is remote, on-site visits for activities like initiation visits are necessary.
- What are the key systems proficiency requirements for a Clinical Research Associate at Worldwide Clinical Trials?
- Proficiency in Microsoft Office Suite, Clinical Trial Management Systems (CTMS), and Electronic Data Capture (EDC) systems is required for this Clinical Research Associate role.
- What is the required experience level for the Senior Clinical Research Associate position?
- The Senior Clinical Research Associate role requires a minimum of 5 years of experience as a Clinical Research Associate. A 4-year university degree or a Nursing Degree is also necessary.
- Can I apply for the Senior Clinical Research Associate role if I do not live on the West Coast?
- No, candidates for this specific Senior Clinical Research Associate position must reside on the West Coast. This is a key requirement for the role.
- What kind of support does Worldwide Clinical Trials offer its CRAs?
- Worldwide Clinical Trials offers extensive support to its CRAs, including assistance with regulatory submissions, TMF management, and access to in-house CRAs for sites with heavy management needs. Regular coaching and clear career paths are also provided.
- What is the career progression for a Clinical Research Associate at Worldwide?
- Worldwide Clinical Trials offers a clear career path for CRAs, with opportunities for development that can lead to roles such as Clinical Trial Manager.
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