Clinical Research Coordinator 2
2 months ago
Who we are
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.
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 Research Coordinator does at Worldwide
The Clinical Research Coordinator 1 (CRC 1), under the guidance of the Clinical Research Coordinator Supervisor or designee, and each clinical trial’s Principal Investigator, is responsible for assisting with assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice guidelines and ICH guidelines as applicable.
What you will do
- Reviews study protocol.
- Performs quality checks on source documents specific to the study, per SOP review must occur in a defined timeframe.
- Attends in-house protocol meeting to review study-related procedures, staffing and visit flow.
- Responsible for giving subject instructions at check-in and serves as the primary contact for subjects by being available to handle study-specific questions, concerns, or events.
- Responsible giving subjects’ safety orientation upon checking into the Clinic.
- Obtains and documents adverse event data on appropriate forms.
- Payment to subjects.
- Responsibilities for dorm assignments, t-shirt allocation, answering queries and laundry schedule.
What you will bring to the role
- Excellent written and oral communication skills.
- Ability to understand complex written and oral instructions.
- Basic computer knowledge and applications required for generation of business correspondence and preparation of regulatory and other study documents.
- Strong interpersonal skills.
- Excellent attention to detail.
- Exceptional organizational skills.
- Ability to set and meet deadlines with high quality work.
- Knowledge of the clinical research process, including Good Clinical Practices, informed consent process, drug accountability procedures, and IRB submission and reporting.
Your experience
- Required: Bachelor’s Degree (preferably in the field of Life Sciences or Health) or 1-2 years of clinical research experience.
- Preferred: 2 to 5 years of clinical research experience.
Why Worldwide
We love knowing that someone is going to have a better life because of the work we do.
For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
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