...Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high... ...now!
The position
The Clinical Research Associate (CRA) is the primary point of contact between... ...and critical issues that may impair trial progress. In some cases, the CRA may have...
...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 safety, you'll be at the forefront of cutting-edge medical research.
Key...
...We are seeking a highly motivated and detail-oriented Clinical Research Associate Intern to join our team. This internship provides a hands-on learning experience within the dynamic field of clinical trials. You will gain exposure to the essential processes involved in conducting...
...the study specific eTMF plans for assigned clinical studies.
Perform quality control of... ...established acceptable criteria
Ensure clinical trial documentation is consistent with eTMF... ...~3+ years of relevant clinical research and TMF experience at a biotechnology, pharmaceutical...
...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...
...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...
...Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience.... ...successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical...
...TMF Specialist Responsibilities:
Receive and process clinical trial documents, ensuring proper filing and indexing.
Perform quality... ...Collaborate with cross-functional teams, including clinical research associates, data managers, and regulatory affairs specialists.
Stay...
..., Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients... ...you’ll be helping shape an industry. The role: The Clinical Trial Manager is responsible for the delivery of all clinical...
Remote job
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines... ...Biology Nursing Public Health
Strong interest in clinical research and drug development.
Excellent organizational and time...
...scholar rock to protein structures, the clinical-stage company is focused on advancing innovative... ...of Position:
The Senior Clinical Trial Manager is responsible for all... ...other clinical team members (e.g. Clinical Research Associates, Data Managers), as well as several external...
...About the role:
The Clinical Operations group is responsible for site management, monitoring tasks and support of clinical trials. The group allocates resources to projects as appropriate to assist with the implementation of project plans and to ensure compliance with regulatory...
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....
Remote job
Clinical CTC-1
Remote job
...full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to join our Global Regulatory Affairs team.
If you are... ...apply today for a life-changing career.
The position
As Associate Regulatory Professional II, you will play a crucial role in driving...
...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....
...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 with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements...
...documents are available for filing in the Trial Master File (TMF) and verify that... ...to monitoring and study plan
Support clinical quality in managing CAPAs and other study... ...in clinical trials industry as Clinical Research Associate
Good working knowledge of GCP and local...
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.
...
...Head - Clinical Research Department
Qualification:
An MBBS graduate with professional experience... ...and assess organizational processes associated with clinical research, create a... ...Responsibilities:
Planning and overseeing the trial and ensure timely and budgetary...
...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...
Company Name: Empower Research and Training Institute.
Empower Research and Training Institute... ...in Bangalore that offers comprehensive clinical research education with hands-on... ...includes a minimum of 2+ years of clinical trials coordination and/or management experience...
Empower Research and Training Institute
Bangalore
2 days ago
...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...
...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...
...Clinical Trial Foundations (CTF), as part of Clinical Design, Delivery and Analytics (CDDA), delivers innovative and reliable systems, processes... ...of new releases and patches by providing technical expertise, associated training, and business process development.
• Resolve system...
...About the job
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience Fortrea provides... ...write update/review and approve all required trial data management documentation; including but...
Rs 5 - 6 lakhs p.a.
...requirements, In-house SOPs and SSPs.
· Conduct audit of Clinical Data Management, Biostat and Programming, Consumer Research, and Software Development activities and... ..., Track and Distribute SOPs and forms
Clinical trial,Data Management
Designation: QA Auditor - Clinical...
Job Description: Clinical Research Scientist
NIRAMAI Health Analytix is looking for a Strong Leader... ...international and national clinical trials
Develop a global network of Key-... ...efficacy.
Be a spokesperson at trade association meetings, public hearings and scientific...
...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...