...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...
...Responsibilities:
Development and effective implementation of Clinical research strategy of the company inline with the overall business goals and strategies.
Provide leadership and develop the clinical research team inline with the business expansion strategy.
End...
...About the job
Role Overview:
Type of Employment: Full-time
Location: Remote
As a Quantitative Clinical Researcher, you will spearhead our quantitative clinical research initiatives. You will be instrumental in:
Conducting rigorous research on digital health...
About the Role
Monitors patient data & study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation...
...We are seeking a motivated and detail-oriented Clinical Research Coordinator to join our dynamic team. As a Clinical Research Coordinator, you will play a crucial role in the planning, implementation, and coordination of clinical research studies. You will work closely with...
...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 looking for an organized, flexible Clinical Research Associate to oversee clinical trials. The Clinical Research Associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials....
...We're seeking motivated students enrolled in a relevant degree to join our team as a Clinical Research Associate Intern. This course-based internship provides a unique opportunity to gain hands-on experience in the dynamic world of clinical trials. If you're passionate about...
...Role Description
This is a full-time hybrid role for a Clinical Research Coordinator with Learning Lab. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research...
...Company Name: Empower Research and Training Institute. Empower Research and Training Institute is a renowned Edu-Tech Start-up in Bangalore that offers comprehensive clinical research education with hands-on experience, industry connections, and expert faculty guidance....
About the Role
Job Purpose:
That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access...
...Job Description: Clinical Research Trainer (Full Time/Part Time) We are looking for qualified and experienced Clinical Research Trainers to join our team. The ideal candidate will have a strong background in Clinical Research, including expertise in Pharmacovigilance, Regulatory...
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...
...knowledgeable, team-oriented, and proactive leader to supervise the clinical aspects of full-service global projects in India. As a Lead CRA... ...presented by Life Sciences Leader and Clinical Leader based on research conducted by ISR reports. The awards recognize CROs that are...
...new ways to continue making a difference, and new people to make a difference with.
How you'll spend your day
To ensure that the clinical study is conducted according to the approved protocol and applicable regulatory requirements.
To protect rights, safety and...
...Job Description
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...
...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...
...Ensure 100% adherence to monitoring and study plan
Support clinical quality in managing CAPAs and other study audit observations... ...with 5 years’ experience in clinical trials industry as Clinical Research Associate
Good working knowledge of GCP and local clinical trial...
...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...
...Specialisation Details
Graduate Graduate - Any
Job Description Responsibilities -
Design and implement business strategies to help the clinic meet organizational goals
Manage staff by assigning and delegating tasks as needed
Develop protocols and procedures to improve...
...Fortis Healthcare Ltd is looking for Assistant Clinical Research to join our dynamic team and embark on a rewarding career journey As an Assistant Clinical Researcher, your job duties and responsibilities may include:
Assisting in Study Design: Collaborating with principal...
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...
...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...
...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...
Fortis Healthcare Ltd is looking for Clinical Research Coordinator to join our dynamic team and embark on a rewarding career journey
We are seeking a highly organized and detail-oriented Clinical Research Coordinator to join our research team
The successful candidate...
AccuScript Consultancy is looking for Clinical Research Analyst to join our dynamic team and embark on a rewarding career journey
A Clinical Research Analyst plays a crucial role in the planning, implementation, and analysis of clinical research studies
The primary responsibilities...
...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...
Rs 2 - 5 lakhs p.a.
...our 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...
...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...