Average salary: Rs1,603,727 /yearly
More stats ...Monitors patient data & study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator... ...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...
...Responsibilities
Support CRAs with the setup, monitoring, and closeout of clinical trials in accordance with Good Clinical Practice (GCP), ICH guidelines, and company SOPs.
Assist in site qualification, initiation, and monitoring visits.
Review and track clinical trial...
...ready for on-call / stay-in night duties.
Managing outpatient clinics and supervising junior doctors.
Assisting in the Operating... ...Malpractice Insurance coverage.
Additional Note:
Clinical Associate in General Surgery role is purely service, non-training job (non...
...and guidelines, and Takeda requirements
ACCOUNTABILITIES:
Lead the development of the study specific eTMF plans for assigned clinical studies.
Perform quality control of documents submitted to the eTMF using the established acceptable criteria
Ensure clinical...
...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...
...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...
...Job Description:
The Clinical Evaluator identifies specific aspects of the clinical data evaluation for their specific review. During... ....
Perform post-market activities like PMS, PSUR, and PMCFin association with other team members.
Conduct PMCF - the clinical...
...knowledgeable, team-oriented, and proactive leader to supervise the clinical aspects of full-service global projects in India. As a Lead CRA... ...as the main communication line between Monitor, Site Management Associate, Regional Project Lead, and/ Project Manager.
Coordinates...
...Job Purpose:
That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global... ...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 this...
...Job Description
Skill required: Clinical Data Services - SAS Clinical
Designation: Clinical Data Svs Associate
Qualifications: BE/BTech/BSc
Years of Experience: 1 to 3 years
About Accenture
Accenture is a global professional services company with leading...
...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...
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...
...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
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... ...years’ experience in clinical trials industry as Clinical Research Associate
Good working knowledge of GCP and local clinical trial rules...
...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...
...procedures like Central line, IV Channelization, Intubation etc.
To be able to operate instruments like Ventilator.
Following all Clinical safety, hygiene, infection control protocols (e.g. wearing gloves when required, aprons, maintaining hand hygiene, etc).
To be...
...maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development...
Compilation and publishing of clinical and safety documents
Coordinate and ensure quality of CTR appendix material
Perform electronic quality control (eQC) of applicable clinical and safety documents
Ensure quality deliverables of Non-clinical reports
To have...
...Clinical Data Management (CDM)
Clinical Data Managers (CDMs) are responsible for ensuring the accuracy, integrity, and completeness of data collected in clinical trials. They work closely with clinical investigators, statisticians, and other members of the clinical trial...
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 associates may be called upon to perform an EKG or to assist a nurse or doctor with a procedure . They provide patient care needs, including phlebotomy assistance, and collect updated and amended regulatory documents in collaboration with the CRA.
Assist attending...
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,...
...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...
...limited to:
Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal... ...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 this...
...ability to train, mentor, and direct the study team and perform ongoing quality control and data review.
Possessing knowledge of Clinical Protocol, data management plan, edit checks requirements, and data standards management.
Having TA-specific knowledge, SOP management...
...that will propel your career to new heights.
Making animals' lives better makes life better – join our team today!
The Associate Manager – Clinical Data Programmer provides technical expertise for the conduct of clinical trials in farm and pet animals and works...
...surgical device, the da Vinci ® Surgical System, to enhance their surgical precision and greatly improve patient benefits. The Clinical Sales Associate will help maximize the utilization of installed da Vinci ® Surgical Systems.
Essential Job Duties
Work with the...
...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...