Clinical Research Associate (CRA)
Clinical Research Associate (CRA)
Posted on :
21-08-2025
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1 Vacancy
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Job Description
Position Overview:
We are looking for a motivated and detail-oriented Clinical Research Associate (CRA) to join our dynamic this role you will manage and monitor clinical research projects ensuring compliance with regulatory requirements and contributing to the successful implementation of data-driven solutions in healthcare. You will work closely with our clients and internal teams to oversee the planning execution and reporting of clinical studies.
Key Responsibilities:
Coordinate and monitor clinical research studies to ensure they meet timelines budgets and regulatory requirements.
Assist in the design and development of study protocols case report forms (CRFs) and other clinical documentation.
Monitor study sites including performing routine visits ensuring data accuracy and maintaining study quality standards.
Collaborate with clients and internal teams to ensure proper implementation and utilization of Sqillines data analytics platforms and clinical research solutions.
Analyze and report study data providing actionable insights to improve study outcomes.
Ensure compliance with Good Clinical Practice (GCP) applicable regulations and ethical guidelines.
Support the training and mentoring of site staff and other team members on clinical processes and tools.
Stay informed about industry trends regulatory updates and advancements in healthcare technology.
Qualifications:
Bachelors or Masters degree in Life Sciences Healthcare or a related field.
At least 2 years of experience as a Clinical Research Associate or in a related role.
Knowledge of clinical trial processes GCP and regulatory requirements.
Familiarity with data analytics platforms machine learning and AI applications in healthcare is a plus.
Strong organizational and time-management skills with attention to detail.
Excellent written and verbal communication skills.
Ability to travel as required for site monitoring and meetings.
We are looking for a motivated and detail-oriented Clinical Research Associate (CRA) to join our dynamic this role you will manage and monitor clinical research projects ensuring compliance with regulatory requirements and contributing to the successful implementation of data-driven solutions in healthcare. You will work closely with our clients and internal teams to oversee the planning execution and reporting of clinical studies.
Key Responsibilities:
Coordinate and monitor clinical research studies to ensure they meet timelines budgets and regulatory requirements.
Assist in the design and development of study protocols case report forms (CRFs) and other clinical documentation.
Monitor study sites including performing routine visits ensuring data accuracy and maintaining study quality standards.
Collaborate with clients and internal teams to ensure proper implementation and utilization of Sqillines data analytics platforms and clinical research solutions.
Analyze and report study data providing actionable insights to improve study outcomes.
Ensure compliance with Good Clinical Practice (GCP) applicable regulations and ethical guidelines.
Support the training and mentoring of site staff and other team members on clinical processes and tools.
Stay informed about industry trends regulatory updates and advancements in healthcare technology.
Qualifications:
Bachelors or Masters degree in Life Sciences Healthcare or a related field.
At least 2 years of experience as a Clinical Research Associate or in a related role.
Knowledge of clinical trial processes GCP and regulatory requirements.
Familiarity with data analytics platforms machine learning and AI applications in healthcare is a plus.
Strong organizational and time-management skills with attention to detail.
Excellent written and verbal communication skills.
Ability to travel as required for site monitoring and meetings.
Required Experience:
IC
Employment Type
Full Time
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