Average salary: Rs824,360 /yearly
More statsSearch Results: 52,487 vacancies
...data & study-related information related to clinical study sites and clinical trial... ...participation.. Ensures the investigator adheres to research protocols, regulatory requirements and... ...achieve this? With our people. It is our associates that drive us each day to reach our ambitions...
...Responsibilities
Support CRAs with the setup, monitoring, and closeout of clinical trials in accordance with Good Clinical Practice (GCP), ICH... ...Biology, Nursing, Public Health]
Strong interest in clinical research and drug development.
Excellent organizational and time...
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements...
...We are hiring for CRAII and Senior CRAs across India.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to...
Summary
That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical... ...the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of...
We're looking for a proactive and highly communicative clinical research professional, pivotal in critically analyzing and summarizing clinical literature to provide valuable insights. Collaborating with cross-functional teams, you will contribute to the systematic review of...
...JOB DESCRIPTION
Brief Position Description:
The Inhouse Clinical Research Associate (IHCRA) provides in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs
Minimum...
...Job Description
Associate Director - Clinical Research
This role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, Company policies and procedures, quality...
...ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations....
...providing key contributions to the advancement of medical research. Our speciality in the procurement and handling of quality... ...Job Description:
iProcess is searching for a skilled Clinical Research Associate (CRA) to take charge of various aspects of biospecimen collection...
...Ensure 100% adherence to monitoring and study plan
Support clinical quality in managing CAPAs and other study audit observations... ...5 years’ experience in clinical trials industry as Clinical Research Associate
Good working knowledge of GCP and local clinical trial rules...
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up and equip trial sites with necessary materials and equipment.
Train site staff on study procedures and data collection methods...
...Job Description
We're looking for a proactive and highly communicative clinical research professional, pivotal in critically analyzing and summarizing clinical literature to provide valuable insights. Collaborating with cross-functional teams, you will contribute to the...
...We have many new ground-breaking global clinical trial projects in various phases and therapeutic... ...Who are we
~ A leading global clinical research organization founded in Asia-Pacific... ...role:
The Senior Clinical Research Associate (SCRA) is a member of the Clinical Operations...
...direct contact with assigned sites, assess and ensure overall integrity of study
2) Implementation and adherence to study protocol at clinical investigational sites, and resolve site issues. Escalate issues that were unresolved to COL/PL.
3) Build and maintain...
Rs 2 - 5 lakhs p.a.
...commitment is to improve patients' lives through a unique Commit-Collaborate-Carry Model.
Job Overview
Junior level Clinical Research Associate role with 1-3 years of experience in the Pharmaceutical & Life Sciences industry. Full-Time position based in Ahmedabad,...
...outcomes of our case studies with the available/existing published research and highlight important points
Translate the data into charts... ...and figures
Study Design and Planning
Develop and design clinical research protocols for holistic healthcare studies.
Plan and...
As a CRA, you will participate in the preparation and execution of Phase I-IV clinical BA/BE studies with a particular focus on monitoring and site management activities to ensure timelines and deliverables are met at assigned sites. You will build and maintain strong relationships...
...Clinical SAS We are looking for a highly skilled and experienced Clinical SAS Programmer to join our growing team. The ideal candidate will have a strong understanding of SAS programming, clinical trial data, and statistical analysis methods. The Clinical SAS Programmer will...
...Study Design: The Clinical Research Associate would be expected to:
Assist with the identification and selection of investigators to undertake the study
Conduct feasibility assessment
Assist in the preparation of documentation for ethics submission
Create, organise...
