Cra jobs in India

Conduct site qualification, initiation, monitoring, and close-out visits, ensuring regulatory and protocol compliance. · Evaluate site performance, escalate serious issues to the project team, and develop action plans. · Verify informed consent process, protect subject/patient co ...

We're proud to foster an inclusive environment driving innovation and excellence, · and we welcome you to join us on our mission to shape the future of clinical development. · ...

This is a full-time role for a Clinical Research Associate I at our Gandhinagar location. · Oversee clinical trials · Ensure compliance with protocols · ...

We're seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities. · Monitoring clinical trial sites. · Conducting site visits. · ...

We're proud to foster an inclusive environment driving innovation and excellence at ICON plc. · We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.As a Senior CRA at ICON Plc, you will play a critical role in overseeing and ma ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, · Monitori ...

Interested Candidates Drop your resume · Designation Trainee CRA · Location Vadodara, Gujarat, India · Work Type Full time · Mode Of Work W. F. O. · Educational Qualification B pharm / M pharm / Bsc / Msc / Life sciences Graduates · Experience needed Freshers to 6 ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advance ...

This role involves overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · Should have min 2yrs of onsite monitoring experience · should have experience in diabetes or obesity therapeutic area. · Immediate ...

Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · Performs site qualification, site initiation, interim monitoring, site management activities ...

We are seeking a motivated Trainee Clinical Research Associate (CRA) to join our team in India. This entry-level position offers an excellent opportunity to gain hands-on experience in clinical research, working alongside experienced professionals in the field. The ideal candidat ...

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · Conducting ...

This Clinical Research Associate II role is responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · ...

We are seeking a Clinical Research Associate I to join our global team and perform various aspects of clinical monitoring and site management. · ...

The Senior Clinical Research Associate will perform site selection initiation monitoring and close-out visits in accordance with contracted scope of work Standard Operating Procedures and all the applicable Good Clinical Practice GCP Guidelines and Regulations. ...

Study Execution and Monitoring: · Conduct site initiation, routine monitoring, and close-out visits according to study protocols, SOPs, ICH-GCP guidelines, and applicable regulatory requirements. · Ensure clinical trials are conducted in adherence to protocol requirements and mon ...

Causality Assessment, Clinical SAS Programming, Communication · Skills, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical ...

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs in clinical trials across 100+ countries. · ...

Monitoring clinical trial sites to ensure adherence to study protocols and regulatory requirements. Conducting site visits and providing training on Good Clinical Practice standards. · ...

We are seeking a Centralized Clinical Trial Manager to oversee centralized monitoring activities of clinical trials and ensure smooth coordination of data-driven insights to enhance trial quality and patient safety. · ...