We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate you will play a pivotal role in designing and analyzing clinical trials interpreting complex medical data and contributing to the advancement of innovative treatments and therapies.
What you will be doing - Conducting site qualification initiation monitoring and close-out visits for clinical trials.
- Ensuring protocol compliance data integrity and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high-quality clinical data.
- Contributing to the preparation and review of study documentation including protocols and clinical study reports
Your profile - Bachelors degree in a scientific or healthcare-related field.
- Minimum of 3 years of experience as a Clinical Research Associate & On-Site Monitoring
- In-depth knowledge of clinical trial processes regulations and ICH-GCP guidelines.
- Oncology/Immunology TA is mandatory
- Strong organizational and communication skills with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate you will play a pivotal role in designing and analyzing clinical trials interpreting complex medical data and contributing to the advancement of innovative treatments and ...
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate you will play a pivotal role in designing and analyzing clinical trials interpreting complex medical data and contributing to the advancement of innovative treatments and therapies.
What you will be doing - Conducting site qualification initiation monitoring and close-out visits for clinical trials.
- Ensuring protocol compliance data integrity and patient safety throughout the trial process.
- Collaborating with investigators and site staff to facilitate smooth study conduct.
- Performing data review and resolution of queries to maintain high-quality clinical data.
- Contributing to the preparation and review of study documentation including protocols and clinical study reports
Your profile - Bachelors degree in a scientific or healthcare-related field.
- Minimum of 3 years of experience as a Clinical Research Associate & On-Site Monitoring
- In-depth knowledge of clinical trial processes regulations and ICH-GCP guidelines.
- Oncology/Immunology TA is mandatory
- Strong organizational and communication skills with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid drivers license
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