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.

YOUR EXPERIENCE

• At least two years independent on-site clinical monitoring experience
• Demonstrable experience of handling multiple protocols across a range of therapeutic indications
• Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree)
• Ability to meet the travel requirements of the job
  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 www.worldwide.com/careers! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
  

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WHAT YOU WILL DO

• Conduct all types of monitoring visits – site qualifications, initiation, interim monitoring, site management and study close-out visits
• Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
• Actively participate in study team and investigator meetings
• Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)

WHAT YOU WILL BRING TO THE ROLE

• Excellent interpersonal, oral, and written communication skills in English and local language
• Superior organizational skills with attention to details, and the ability to work independently
• Broad understanding of clinical research principles and process
• Proficiency in Microsoft Office, CTMS and EDC Systems