Worldwide Clinical TrialsWT

Clinical Trials Associate REMOTE US

Worldwide Clinical Trials is a full-service global Contract Research Organization (CRO) established to support biotechnology and pharmaceutical companies in advancing new medications from discovery to reality.

Worldwide Clinical Trials

Employee count: 1001-5000

United States only

Who we are

We’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 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!

What the Clinical Trial Associate does at Worldwide

As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

What you will do

  • Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)

  • Maintain and quality audit to assure the most recent revisions of documents are on project portals

  • Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File

  • Maintain version and quality control of project documentation and submit to trial master file

  • Assist with the tracking and maintenance of project related information, including site medical question and answer log

What you will bring to the role

  • Excellent written and verbal English as well as fluency of the language of the country of location

  • Ability to handle multiple tasks and exercise independent judgment

  • Strong attention to detail and focus on quality of work

  • Strong organizational and problem-solving skills

  • Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

Your experience

  • Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role

  • Skill sets and proven performance equivalent to the above

We 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.

About the job

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Posted on

Job type

Full Time

Experience level

Entry-level

Location requirements

Hiring timezones

United States +/- 0 hours

About Worldwide Clinical Trials

Learn more about Worldwide Clinical Trials and their company culture.

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Worldwide Clinical Trials is a full-service global Contract Research Organization (CRO) established to support biotechnology and pharmaceutical companies in advancing new medications from discovery to reality. With over 30 years of expertise, we leverage decades of clinical research and therapeutic knowledge to deliver customized solutions tailored to the specific needs of our clients. Our commitment to personalized support is paramount; each study is approached with an understanding that individualized attention is crucial to success.

At Worldwide, we embrace a collaborative philosophy that encourages innovation and direct communication. We prioritize building strong relationships by pairing clients with experienced Therapeutic Leads who are experts in their respective fields. This ensures not only a deep understanding of the disease state but also that the challenges of each clinical trial are met with strategic insight. Our operational model is designed to remain flexible and responsive, adapting to any changes that may arise during the trial process. We are committed to ethical practices and transparency, making certain that every step in the clinical research process is conducted with the highest levels of integrity.

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Worldwide Clinical Trials

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Worldwide Clinical Trials hiring Clinical Trials Associate REMOTE US • Remote (Work from Home) | Himalayas