[Hiring] In-House Clinical Research Associate I @Worldwide Clinical Trials

Role Description

Embark on a fulfilling Clinical Operations career as you leave a lasting impact on patients’ lives. Join Worldwide Clinical Trials for an unparalleled CRO experience, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial.

• Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel.
• Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.).
• Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
• Perform feasibility studies/site identification activities for potential sites, as requested.

Qualifications

• Excellent interpersonal, oral, and written communication skills.
• Ability to contribute to a team remotely.
• Strong customer focus, ability to interact professionally with a sponsor contact.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

Requirements

• Four-year college curriculum with a major concentration in life science preferred but not required, OR
• Two-year college curriculum or equivalent education/training and one year experience with clinical research (e.g. study coordinator, CTA, etc.) or other experience deemed relevant.
• Proficiency in English and Polish and one other language (German, French, Italian, Spanish).

Benefits

• Commitment to enabling professionals from all backgrounds and experiences to succeed.
• Prioritization of cultivating a diverse and inclusive environment that promotes collaboration and creativity.
• Exceptional employee experiences where everyone is respected and has access to equal opportunity.