Senior Clinical Research Associate – Oncology

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

📋 Description

• Oversee research operations at locations engaged in Worldwide’s clinical research initiatives

• Engage in every phase of clinical trials, encompassing site selection, study initiation, site upkeep, and study conclusion

• Gather necessary regulatory documents from participating sites

• Aid in the negotiation of contracts and budget agreements

• Educate sites on accurate data collection and the reporting of potential safety-related incidents

• Execute study initiation visits (SIVs)

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

• Conduct most site management activities remotely

⛳️ Requirements

• Exceptional interpersonal, verbal, and written communication abilities in English

• Outstanding organizational capabilities with a keen attention to detail

• Capacity to operate with minimal or no supervision

• Proficient in Microsoft Office, CTMS, and EDC Systems

• Over 5 years of experience as a Clinical Research Associate

• Bachelor’s degree or Nursing degree required

• Experience in Oncology is mandatory

• Candidates must be located in the Midwest or Central Regions

• Willingness to travel regionally is essential

🏝️ Benefits

• Competitive benefits package based on location

• Opportunities for professional growth through regular check-ins and coaching discussions with the Line Manager

• Defined career progression that can lead to Clinical Trial Manager positions

• Collaborative and supportive work environment

• Involvement in regulatory submissions, TMF management, and internal CRA support