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Senior Clinical Research Associate - CNS/Psychiatry - Midwest U.S. Remote

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 Do• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional / observational studies• 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, will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirementsWhat You Will Bring To The Role• Excellent interpersonal, oral, and written communication skills in English• Superior organizational skills with attention to details• Ability to work with little or no supervision• Proficiency in Microsoft Office, CTMS and EDC SystemsYour Experience• 5+ years of experience as a Clinical Research Associate• 4-year university degree or RN/BSN in Nursing• Experience in CNS is required, Psychiatry is strongly preferred• Willingness to travel requiredWe 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 www.Worldwide.com 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.
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CEO of Worldwide Clinical Trials
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Neal R. Cutler, M.D.
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What You Should Know About Senior Clinical Research Associate - CNS/Psychiatry - Midwest U.S. Remote, Worldwide Clinical Trials

Are you an experienced Senior Clinical Research Associate specializing in CNS and Psychiatry, seeking a fresh opportunity? At Worldwide Clinical Trials, a global midsize CRO based in Burnsville, NC, we pride ourselves on innovation and a commitment to revolutionizing how research is done. Join a team of dynamic professionals, where you'll have the chance to impact lives through the management of clinical research activities at various sites. You'll oversee every stage of the clinical study, from the exciting beginning phases of site identification and regulatory document collection to offering your expertise during study maintenance. Your role will predominantly focus on registries and non-interventional observational studies, providing a unique and engaging experience. Here at Worldwide, we offer extensive support with regulatory submissions, thoughtful team collaboration, and an emphasis on your professional growth. Our mission is simple - to improve patient lives through passion and purpose. You’ll find a supportive environment where ideas are welcomed and creativity is encouraged. Plus, with a clear career path leading toward Clinical Trial Manager roles, you’ll be empowered to advance your career while working remotely across the Midwest U.S. It's all about making a difference and being part of an inclusive culture that values every team member's unique contributions. If this sounds like the role for you, we’d love to hear from you! Together, we can make a world of difference in CROs and patient care.

Frequently Asked Questions (FAQs) for Senior Clinical Research Associate - CNS/Psychiatry - Midwest U.S. Remote Role at Worldwide Clinical Trials
What are the responsibilities of a Senior Clinical Research Associate at Worldwide Clinical Trials?

As a Senior Clinical Research Associate at Worldwide Clinical Trials, your responsibilities will encompass managing research activities at sites involved in clinical projects, primarily focused on registries and non-interventional studies. You will conduct study initiation visits, oversee study start-up activities, and ensure compliance with regulatory requirements while managing site performance throughout the research process.

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What qualifications are required to apply for the Senior Clinical Research Associate position at Worldwide Clinical Trials?

To qualify for the Senior Clinical Research Associate position at Worldwide Clinical Trials, candidates need a minimum of 5 years of experience in a CRA role along with a 4-year university degree or an RN/BSN in Nursing. Specific experience in CNS is required, with a preference for those with a background in Psychiatry.

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Is remote work an option for the Senior Clinical Research Associate position at Worldwide Clinical Trials?

Yes, the Senior Clinical Research Associate role at Worldwide Clinical Trials allows for remote work across the Midwest U.S. While most site management efforts can be conducted remotely, occasional site visits may be required to ensure compliance and proper data collection.

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How does Worldwide Clinical Trials support the professional development of Senior Clinical Research Associates?

Worldwide Clinical Trials places a strong emphasis on professional development for their Senior Clinical Research Associates by offering continuous coaching conversations with line managers and a clear career advancement path leading to Clinical Trial Manager roles, ensuring you are well-prepared for the next step in your career.

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What is the company culture like at Worldwide Clinical Trials for Senior Clinical Research Associates?

The company culture at Worldwide Clinical Trials is inclusive, supportive, and collaborative. We prioritize a diverse work environment where every individual is encouraged to thrive and express their ideas while contributing to the mission of improving patient lives.

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Common Interview Questions for Senior Clinical Research Associate - CNS/Psychiatry - Midwest U.S. Remote
What motivates you to pursue a career as a Senior Clinical Research Associate?

When answering this question, emphasize your passion for contributing to patient outcomes and the research process. Discuss specific experiences that ignited your interest in clinical trials and how they align with Worldwide Clinical Trials' mission.

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Can you describe your experience with managing multiple clinical trial sites?

In your response, detail your organizational abilities and previous experiences managing various sites simultaneously. Include specific examples of strategies you used to keep each study on track, demonstrating your impact on overall project efficiency.

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How do you handle regulatory compliance when managing clinical sites?

Discuss your thorough knowledge of regulatory frameworks and detail how you ensure compliance, including examples where you successfully navigated challenges at sites. Highlight your communication skills and ability to foster cooperation among stakeholders.

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What strategies do you use to ensure accurate and timely data collection from sites?

Explain your systematic approach to data collection, including training site staff, following-up for data submission, and utilizing technology effectively. Use specific examples that reflect your attention to detail and commitment to quality data.

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How would you approach building relationships with site staff?

Highlight your interpersonal skills and provide examples of how you build rapport with site staff. Emphasize the importance of trust and open communication, which contribute to a successful working relationship and research outcomes.

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What challenges have you faced as a Clinical Research Associate and how did you overcome them?

Reflect on a specific challenge you faced, detailing what made it difficult and the steps you took to overcome it. Focus on your problem-solving skills and resilience, and how these experiences have better prepared you for future challenges.

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How do you stay updated with industry changes and advancements in clinical research?

Discuss your commitment to continuous learning through attending conferences, participating in webinars, or following industry publications. Mention specific resources or networks you engage with that keep you informed about the latest trends in clinical research.

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What experience do you have with non-interventional or observational studies?

Share your prior experiences working specifically with non-interventional studies. Discuss roles you’ve held and key learnings from these studies that highlight your expertise in this area and how it aligns with the needs of Worldwide Clinical Trials.

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Describe a time you had to train site staff. What approach did you take?

Provide a detailed response on your training experience, including your preparation, presentation style, and how you ensured comprehension. Use a specific example to showcase your effective training techniques and their impact on data collection.

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What are your long-term career goals as a Senior Clinical Research Associate?

In your answer, express your aspirations of advancing within the clinical research field and how the opportunities at Worldwide Clinical Trials will help you achieve these goals. Reflect on a desire to lead projects, mentor junior associates, or specialize further.

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Our mission is to work with passion and purpose every day to improve lives.

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Full-time, remote
DATE POSTED
December 13, 2024

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