Clinical Trial Manager-Reputed Medical

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. - With our patients at the centre of all that we do, we help to accelerate the...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

Associate/Content Editor in the Clinical Trials team We are looking for an Associate Content Analyst/Content Analyst to join our Clinical Trails team in Hyderabad/Chennai/Bangalore. This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. We have a great skill set in Clinical and we would...

Associate/Content Editor in the Clinical Trials team We are looking for an Associate Content Analyst/Content Analyst to join our Clinical Trails team in Hyderabad/Chennai/Bangalore. This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. We have a great skill set in Clinical and we would...

JOB DETAILS 1.writing drug trial methodologies (procedures)2.identifying and briefing appropriate trial investigators (clinicians)3.setting up and disbanding trial study centres4.designing trial materials and supplying study centres with sufficient quantities5.providing clinicians with instructions on how to conduct the trials6.collecting and...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Integrity, Collaboration, Agility...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Integrity, Collaboration, Agility...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Integrity, Collaboration, Agility...

JOB DETAILS 1.writing drug trial methodologies (procedures)2.identifying and briefing appropriate trial investigators (clinicians)3.setting up and disbanding trial study centres4.designing trial materials and supplying study centres with sufficient quantities5.providing clinicians with instructions on how to conduct the trials6.collecting and...

JOB DETAILS 1.writing drug trial methodologies (procedures)2.identifying and briefing appropriate trial investigators (clinicians)3.setting up and disbanding trial study centres4.designing trial materials and supplying study centres with sufficient quantities5.providing clinicians with instructions on how to conduct the trials6.collecting and...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.Review...

**Knowledge and Skills** Knowledge of medical terminology. Understanding of clinical trials methodology and terminology. Understanding and experience in using data standards. Competent in clinical study management that includes clinical data management. Generate specifications for EDC build components (e.g., Rights and Roles). Experience in forms...

Role Summary: - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide statistical...

Role Summary: - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide...

JOB DETAILS1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.3. Review...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP...

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP...

ROLE SUMMARY - Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards and best practices. - Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. - Provide...

Job Location : ChennaiWork Mode : OnsiteAs a Medical Writer at ACL Digital, the role in the development and review of clinical and regulatory documents essential for the advancement of medical research and product development. Your responsibilities will include writing and reviewing a variety of documents such as clinical trial protocols, clinical study...