Remote Jobs
Employer Industry: Clinical Research and Healthcare Intelligence
Why consider this job opportunity
Competitive salary with additional benefits focused on well‑being and work‑life balance
Opportunity for career advancement and growth within a reputable organization
Flexible working environment with various annual leave entitlements
Comprehensive health insurance offerings to suit personal and family needs
Access to a Global Employee Assistance Programme for support and well‑being
Inclusive and diverse workplace culture that values high performance and nurtures talent
What to Expect (Job Responsibilities)
Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolve queries to maintain high‑quality clinical data
Contribute to the preparation and review of study documentation, including protocols and clinical study reports
What is Required (Qualifications)
Bachelor's degree in a scientific or healthcare‑related field
Minimum of 12 months onsite monitoring experience as a Clinical Research Associate (CRA I, CRA II, or Senior CRA)
In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines
Strong organizational and communication skills with attention to detail
Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license
How to Stand Out (Preferred Qualifications)
Experience working in a fast‑paced environment
Proficiency in clinical trial management systems and electronic data capture
Familiarity with regulatory submission processes
Additional certifications related to clinical research
We prioritize candidate privacy and champion equal‑opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top‑tier employer.
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Why consider this job opportunity
Competitive salary with additional benefits focused on well‑being and work‑life balance
Opportunity for career advancement and growth within a reputable organization
Flexible working environment with various annual leave entitlements
Comprehensive health insurance offerings to suit personal and family needs
Access to a Global Employee Assistance Programme for support and well‑being
Inclusive and diverse workplace culture that values high performance and nurtures talent
What to Expect (Job Responsibilities)
Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolve queries to maintain high‑quality clinical data
Contribute to the preparation and review of study documentation, including protocols and clinical study reports
What is Required (Qualifications)
Bachelor's degree in a scientific or healthcare‑related field
Minimum of 12 months onsite monitoring experience as a Clinical Research Associate (CRA I, CRA II, or Senior CRA)
In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines
Strong organizational and communication skills with attention to detail
Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license
How to Stand Out (Preferred Qualifications)
Experience working in a fast‑paced environment
Proficiency in clinical trial management systems and electronic data capture
Familiarity with regulatory submission processes
Additional certifications related to clinical research
We prioritize candidate privacy and champion equal‑opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately.
We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top‑tier employer.
#J-18808-Ljbffr