Summary
To lead a community of ~ 20 Clinical Data Acquisition Specialists, Clinical Data Scientists and Coding Specialists as assigned... ...across their community of Clinical Data Acquisition and Management associates/roles (Clinical Data Scientists, Clinical Data Acquisition...
...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...
...Clinical Data Management We are looking for a detail-oriented and organized Clinical Data Manager (CDM) to join our expanding clinical research team. The ideal candidate will be a passionate advocate for data accuracy and integrity, ensuring the smooth and efficient flow...
...Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience.... ...Perform routine monitoring visits to assess site performance, data integrity, and regulatory compliance. Ensure timely...
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up and... ...and equipment.
Train site staff on study procedures and data collection methods.
Develop and maintain study manuals and...
...Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget,... ...standards (SOPs) and best practices for clinical operations/clinical data review activities within assigned clinical trial(s) and within clinical...
...Report Form (eCRF) development with a thorough understanding of data to be collected and in alignment with the protocol.
Support the... ...new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data Standards...
...We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe... ...activities and other fun events!
About the role:
The Clinical Data Manager-II is responsible for assisting in the set-up,...
...Summary:
In accordance with project specific timelines and data review plans, perform data management
activities to ensure the generation of accurate, complete, and consistent clinical databases.
To fulfil his/her job responsibilities in accordance with Good Clinical...
...Clinical Data Programmer (CDM)
Database Design and Development:
Collaborate with clinical research teams to understand study protocols and data collection methods.
~ Design and build clinical databases to efficiently store and manage collected data.
~ Develop data...
Rs 3 - 4 lakhs p.a.
...physician as a reference document.
Populate the summarized data in the electronic health record
Generate the chart note... ...BUMS,BPT,ANY DOCTOR DEGREE
Designation: Vacancy for Doctors - Clinical Associate
Vacancies: 50
Experience: 0 - 4.0 Year(s)
Telephonic Interview...
...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 documentation...
...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....
...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... ...records.
Participate in clinical research projects, data collection, and quality improvement initiatives related to neurosurgical...
...Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and... ...balancing across assigned teams in coordination with Clinical Data Management Team Leaders.
• Provide resource projection on an...
...with other IT employees.
Successfully collaborates with vendor partners throughout testing and deployment.
Follows all GCP (Good Clinical Practice) regulations and the Software Development Life Cycle (SDLC) SOPs for the development and validation of the database...
...Execute trial TMF QC activities in accordance with TCO portfolio and Clinical Operations Transition Decision Point (TDP) and Clinical Study... ..., work streams and governances. May perform Clinical Project Associate (CPA) tasks as assigned
Commitment to Diversity & Inclusion...
...About the job
Summary
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...
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely... ...regulatory requirements, and GCP guidelines. Perform source data verification and data review to ensure accuracy and completeness...
About the department
Data Systems & Automation, Bangalore Global Development is one of the most competent and diverse team of professionals... ...for providing functional and system support to execute clinical trials across Product Development Plan portfolio. The team has strong...
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research... ....
Job Description
•Develops and implements ICON end-to-end data standards libraries from data collection to analysis
•Provides...
Remote job
...Description
Were looking for a proactive and highly communicative clinical research professional pivotal in critically analyzing and... ...Research Analysis
Open Positions
2
Skills Required
Data Validation
Role
Conduct systematic literature reviews (SLR...
...conducting the study(ies) and reporting study data as required by the study protocol,... ...to monitoring and study plan
Support clinical quality in managing CAPAs and other study... ...clinical trials industry as Clinical Research Associate
Good working knowledge of GCP and...
Position : Clinical Data Analyst EPIC ClarityLocation : Pune/Hyderabad/GurgaonExperience : 3+Job Description :We are seeking a skilled and experienced Clinical Data Analyst to join our team and support our Epic Systems implementation. The ideal candidate will have a strong...
...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...
...About the role
Clinical Data Scientist
Location – Hyderabad/ Mumbai
About the Role:
Provide timely and professional ongoing management... ...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...
...Overview ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive... ...Responsibilities:
What you will be doing:
Review CRF/eCRF data for completeness, accuracy and consistency via computerized edits...
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.
With...
Remote job
...of a project, from regulatory affairs and clinical operations to quality assurance and... ...Full Service Pro vider Senior Clinical Data Manager (Sr CDM) role, based in Bangalore... ...Understanding of recommended CDM best practices and associated documentation.
Experience in clinical...
...Position: Clinical Data Manager
Requirement: Immediate Joiner
Location: Hyderabad
Experience: 3 to 10 Years
Key Roles & Responsibilities:
Provide leadership and vision to the team.
Manage and deliver largescale highcomplexity studies across a range of sponsors...