Average salary: Rs382,777 /yearly
More stats ...TMF Specialist Responsibilities:
Receive and process clinical trial documents, ensuring proper filing and indexing.
Perform quality checks on documents to ensure they meet regulatory requirements and study protocols.
Maintain and update the TMF according to established...
...Join our international team and be the key support to clinical research projects, streamlining communication... ...information.
Office Based in Bangalore
You will:
Assist clinical project teams with selective aspects of trial management from start-up to close-out on a country...
...the study specific eTMF plans for assigned clinical studies.
Perform quality control of... ...established acceptable criteria
Ensure clinical trial documentation is consistent with eTMF... .../ or other functional teams as needed
Assist with inspection/audit related activities (...
...Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and... ...and you’ll be helping shape an industry. The role: The Clinical Trial Manager is responsible for the delivery of all clinical aspects...
Remote job
...Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and... ...other activity or lack thereof which may jeopardise the clinical trial delivery or patient safety .
• *Ensure all necessary trainings...
About the job
Job Description Senior Business Analyst
Required Skills:
5+ years of experience with minimal 4-year experience in Client Management and Business/System Analysis Role.
At least 3 year of experience in HealthCare or Pharmaceutical (CRO) industry.
...
...to ensure that people living with a chronic disease can live a full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to join our Global Regulatory Affairs team.
If you are passionate about driving change and navigating complex agendas, apply today...
Job Description
Job Description
CTC II
...Clinical Trial Foundations (CTF), as part of Clinical Design, Delivery and Analytics (CDDA), delivers innovative and reliable systems, processes, and information to enable clinical development and speed medicines to patients. The Clinical Systems Management role will support...
...comprehensive PO creation, invoice management and PO reconciliation and PO closure across a variety of vendor categories including CROs, clinical trial sites, contract labs, IRB/EC and other key assignments. Collaborate cross-functionally to develop strong internal and external...
Rs 5 - 6 lakhs p.a.
...Regulatory requirements, In-house SOPs and SSPs.
· Conduct audit of Clinical Data Management, Biostat and Programming, Consumer Research, and... ...).
· Maintain, Track and Distribute SOPs and forms
Clinical trial,Data Management
Designation: QA Auditor - Clinical Trials...
...comprehensive PO creation, invoice management and PO reconciliation and PO closure across a variety of vendor categories including CROs, clinical trial sites, contract labs, IRB/EC and other key assignments. Collaborate cross-functionally to strengthen strong internal and external...
...Job Description
~ Dental assistant and recptionist job for a 8 year old clinic in Mumbai
Job Requirement
Experience
Fresher
Internship
No
Skills
none
Comfortable with
Specialized Course(s)
none
Fire Arm License
Fire Arm
Height...
Medical graduate degree
2 years+ experience in investigation/audit or clinical practice
Rs 2.4 - 3.5 lakhs p.a.
...Job Description
We have an opening for the position of Assistant Clinic -In-Charge for (Health Care Industry ) for the Guwahati location.
Responsibilities :
~ Daily Reports and Monthly Reports to the Board of Directors.
~Share the M.O.M of clinic meetings...
...Post : Clinical Research Associate/Clinical Trial
Location : Ahmedabad-(Science City Road, Sola)
Exp : 3Yrs to 8Yrs
Roles & Responsibilities:
- Perform on-site in-process and retrospective monitoring visit of clinical phase of the clinical trials, PK and BA/BE studies...
...individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of...
...and the UK, our 700+ people support 245+ active projects and clinical trials across 50+ countries, with 400+ more staff across our social enterprises... ...and improving health outcomes worldwide. A Clinical Trial Assistant will work on trials testing new and existing drugs and will...
...Australia, and India servicing clients in over 60 countries, we are seeking talented individuals to join our company.
Editorial Assistant , Clinical Medicine
The Role
We are currently looking for a bright, self-motivated, hard-working individual for an entry-level...
...We are looking for Clinical Assistant to join our dynamic team and embark on a rewarding career journey
Take vital signs and record medical histories of patients, and update electronic medical records as needed
Assist physicians or other medical professionals in clinical...
...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...
...Job Description
Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo Nordisk... ...inspiring working environment, you may be our new Project Manager (CDC Trial Manager) for the Clinical Medical Regulatory team based at Mumbai...
...Clinical Team Leader will be responsible for overseeing the monitoring and site management activities... ...of issues.
Demonstrates ability to assist CPM and team with projecting timelines and... ...for all study and coordination with trial site related activities to the assigned CPM...
...• Works closely with other departments and project lead to oversee financial aspects of functional area's portion of projects.
• Assists project team to identify risks, define reasons for unsupported hours, and attends risk meetings as needed.
• Prepares estimates for...
...and the UK, our 700+ people support 245+ active projects and clinical trials across 50+ countries, with 400+ more staff across our social enterprises... ...:
- Provide mentoring and guidance to early career staff, assisting them in their professional development and career progression....
...As a Clinical Research Associate, you'll play a pivotal role in ensuring the successful execution of clinical trials. From monitoring trial progress to ensuring regulatory compliance and participant... ...investigators and site staff.
Assist in regulatory submissions and ensure...
...seeking a highly motivated and detail-oriented Clinical Research Associate Intern to join our team... ...within the dynamic field of clinical trials. You will gain exposure to the essential processes... ...patient safety.
Key Responsibilitie
Assist with the preparation and submission of...
...Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high performing team in Novo Nordisk that plays a critical... ...to them progress and critical issues that may impair trial progress. In some cases, the CRA may have direct contact with the...
...generation of accurate, complete, and consistent clinical databases.
To fulfil his/her job... ...timesheet management system.
Assist Data Management Study Lead in development... ...and Data Validation Plan (DVP) for assigned trials which include taking an active part in any...
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up and equip trial sites... ...and regulatory authorities.
Post-Trial:
Assist with data analysis and study close-out activities....