Clinical Research Associate Role
As a Clinical Research Associate, you play a vital role in safeguarding the rights and well-being of trial participants, ensuring accurate, complete, and verifiable trial data from source documents.
Key Responsibilities:
* Develop strong relationships with Principal Investigators, study coordinators, pharmacists, and site personnel to efficiently manage clinical trials.
* Foster customer relationships to ensure timely project delivery as per study requirements and timelines.
* Collaborate with internal teams to prepare site essential documents and support ethics and regulatory submission processes.
* Drive site recruitment and engagement initiatives, preparing site-specific plans to meet participant targets.
* Monitor investigational sites according to ICH GCP guidelines, including site selection, initiation, monitoring, and close-out visits.
Essential Skills and Qualifications:
* Bachelor's degree in a clinical or life sciences-related field.
* Relevant experience or qualifications in allied professions may be considered.
* Strong time management skills, attention to detail, team work, and computer literacy.
* Minimum 6 months of independent CRA monitoring experience for CRA II, 2+ years for CRA III, and 4+ years for SCRA.
Benefits and Work Arrangements:
* Hybrid working arrangements and flexible working hours for a healthy work-life balance.
About Our Organization:
* We are committed to offering a great workplace and promoting gender equality.
* An inclusive work environment where everyone is treated fairly and respected.
* We support team members with flexible options, paid parental leave, wellness programs, and ongoing development opportunities.