Senior Clinical Research Associate

March 4

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Logo of Worldwide Clinical Trials

Worldwide Clinical Trials

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

Neuroscience/Central Nervous System Clinical Research • Rare Disease Clinical Research • Oncology Clinical Research • IMID Clinical Research • Cardiovascular and Metabolic Clinical Research

📋 Description

• Conduct all types of 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).

🎯 Requirements

• At least two years independent 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.

🏖️ Benefits

• Equal employment opportunities for 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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February 25

Oversee clinical site monitoring services for projects at Alimentiv. Act as primary liaison for CRAs and project team.

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