Clinical Research Associate II – Cardio

This is a fully remote position, open to applicants in Tennessee, +1 more state.

📋 Description

• Oversee research activities at sites involved in Worldwide’s clinical research initiatives.

• Identify and evaluate potential sites for participation in studies.

• Execute study start-up tasks, which include gathering regulatory documents and facilitating contract and budget negotiations.

• Provide training to sites on accurate data collection and reporting of potential safety-related incidents.

• Manage site operations throughout the duration of the study.

• Conclude research activities at sites after the study has ended.

• Conduct study initiation visits (SIVs).

• Ensure adherence to informed consent processes, safety-event reporting, and relevant regulatory standards.

• Carry out the majority of site management tasks remotely.

⛳️ Requirements

• Exceptional interpersonal, oral, and written communication skills in English.

• Outstanding organizational abilities with a keen eye for detail.

• Capability to work independently with minimal supervision.

• Proficiency in Microsoft Office, CTMS, and EDC Systems.

• A minimum of 2 years of experience as a Clinical Research Associate.

• Bachelor’s degree or Nursing degree is required.

• Experience in Cardiology or Hypertension is mandatory.

• Candidates must be located in the East Coast or Central United States.

• Willingness to travel regionally is essential.

🏝️ Benefits

• Comprehensive support for regulatory submissions, TMF management, and in-house CRAs for projects with significant site management requirements.

• Regular check-ins and coaching discussions with the Line Manager.

• Clearly defined career progression and professional development opportunities leading to Clinical Trial Manager positions.

• Access to the Executive Leadership team.

• Competitive benefits package based on location.