ICON Strategic Solutions is the world’s largest and most comprehensive clinical research organization (CRO), driven by healthcare intelligence. With a global presence and a commitment to innovation and continuous improvement, ICON offers its employees the opportunity to be a part of a dynamic and supportive environment. The company thrives on collaboration, empowering its team members to reach their full potential and contribute to saving lives.
Responsibilities in the Job
As a Clinical Research Associate (CRA) at ICON Strategic Solutions, you will be responsible for overseeing various aspects of clinical trials, ensuring high-quality data collection and adherence to regulatory standards. Your key duties will include:
- Site Selection & Initiation: You will be involved in selecting and initiating study sites, ensuring all aspects of the study are set up properly.
- Monitoring Visits: Perform routine monitoring visits and manage site activities from initiation through to database lock, ensuring compliance and quality at every stage.
- Study Site Management: You will ensure that study sites maintain high-quality data, resulting in consistently low query levels and high-quality assurance reports.
- Team Support: As a CRA, you will also be responsible for mentoring and supporting team members, helping them perform at their best.
Qualifications
The ideal candidate should have the following qualifications:
- Education: A degree in B.Pharm, M.Pharm, Pharm D, BDS, or MBBS.
- Experience: A minimum of 2 years of onsite monitoring experience (excluding training and induction) specifically in the field of Oncology.
- Skills: Strong communication skills, both verbal and written, are essential for managing site interactions and reporting. You must also be comfortable working independently and within a team.
Skills
To be successful in this role, candidates should possess:
- Oncology Expertise: Experience in oncology clinical trials and familiarity with monitoring protocols specific to cancer treatments.
- Attention to Detail: Ability to review and interpret data, ensuring all aspects of the study meet regulatory standards and quality benchmarks.
- Communication: Strong communication skills to collaborate effectively with the study team, site personnel, and other stakeholders.
- Problem Solving: A proactive approach to identifying issues and finding solutions that maintain the integrity of the clinical trial.
ICON Strategic Solutions is the world’s largest and most comprehensive clinical research organization (CRO), driven by healthcare intelligence. With a global presence and a commitment to innovation and continuous improvement, ICON offers its employees the opportunity to be a part of a dynamic and supportive environment. The company thrives on collaboration, empowering its team members to reach their full potential and contribute to saving lives.
Responsibilities in the Job
As a Clinical Research Associate (CRA) at ICON Strategic Solutions, you will be responsible for overseeing various aspects of clinical trials, ensuring high-quality data collection and adherence to regulatory standards. Your key duties will include:
- Site Selection & Initiation: You will be involved in selecting and initiating study sites, ensuring all aspects of the study are set up properly.
- Monitoring Visits: Perform routine monitoring visits and manage site activities from initiation through to database lock, ensuring compliance and quality at every stage.
- Study Site Management: You will ensure that study sites maintain high-quality data, resulting in consistently low query levels and high-quality assurance reports.
- Team Support: As a CRA, you will also be responsible for mentoring and supporting team members, helping them perform at their best.
Qualifications
The ideal candidate should have the following qualifications:
- Education: A degree in B.Pharm, M.Pharm, Pharm D, BDS, or MBBS.
- Experience: A minimum of 2 years of onsite monitoring experience (excluding training and induction) specifically in the field of Oncology.
- Skills: Strong communication skills, both verbal and written, are essential for managing site interactions and reporting. You must also be comfortable working independently and within a team.
Skills
To be successful in this role, candidates should possess:
Problem Solving: A proactive approach to identifying issues and finding solutions that maintain the integrity of the clinical trial.
Oncology Expertise: Experience in oncology clinical trials and familiarity with monitoring protocols specific to cancer treatments.
Attention to Detail: Ability to review and interpret data, ensuring all aspects of the study meet regulatory standards and quality benchmarks.
Communication: Strong communication skills to collaborate effectively with the study team, site personnel, and other stakeholders.
