[Hiring] Clinical Research Associate II @Worldwide Clinical Trials

Role Description

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including:

• Cardiovascular
• Metabolic
• Neuroscience
• Oncology
• Rare Diseases

Your contributions will leave a profound impact on the lives of patients. Responsibilities include:

• Managing the research activities at sites participating in Worldwide’s clinical research projects.
• Involvement in all stages of the clinical study, including:
• Identifying potential sites to participate in the research effort.
• Performing various study start-up activities such as working with sites to collect appropriate regulatory documents.
• Supporting the negotiation of contracts and budgets.
• Training the sites to collect data properly and report any potential safety-related events.
• Managing the site's activities during study maintenance.
• Closing down research activities at the sites once the study has concluded.
• Conducting study initiation visits (SIVs).
• Ensuring compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements.

Qualifications

• Excellent interpersonal, oral, and written communication skills in English.
• Superior organizational skills with attention to detail.
• Ability to work with little or no supervision.
• Proficiency in Microsoft Office, CTMS, and EDC Systems.

Requirements

• 2+ years of experience as a Clinical Research Associate.
• 4-year university degree OR Nursing Degree.
• Experience in Cardiology or Hypertension required.
• Candidates must reside in the East Coast or Central United States.
• Willingness to travel regionally required.

Benefits

• Competitive salary range: $79,500.00 - $158,500.00 annually.
• Transparent compensation practices.
• Competitive benefits package depending on location.
• Pay equity and transparency.