...PKS is a global organization of about 300 associates, situated within Translational Medicine (... ..., pharmacodynamics, metabolism and clinical pharmacology in advancing the drug candidates... ...clinical trials for biologics . Coordinate and monitor PK, PD, anti-drug (ADA) and neutralizing...
...Department – Clinical Medical Regulatory (CMR)
Do you want to be a part of a high... ...The position
The Clinical Research Associate (CRA) is the primary point of contact between... ...accordance with the protocol to perform monitoring activities required.
Proactive use of...
...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...
...is our firm belief that these qualities are non-negotiable, cannot be taught but the rest can be.
The Due Diligence/ Transaction Monitoring/ Screening Analyst is responsible for conducting end to end DD/TM/Screening for different entities or individuals, all levels. You will...
...Clinical Research Associate Template
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...
...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...
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical... ...ensures what we do, we do well.
Key responsibilities:
Site Monitoring
SIV ~ COV
PI Management
audit & inspection
NDCT...
Remote job
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up... ...Develop and maintain study manuals and documentation.
Monitoring:
Conduct regular visits to trial sites to monitor progress...
...We have many new ground-breaking global clinical trial projects in various phases and therapeutic... ...role:
The Senior Clinical Research Associate (SCRA) is a member of the Clinical... ...group is responsible for site management, monitoring tasks and support of clinical trials....
...Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience.... ...role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong...
...Job Description
Department – Clinical Reporting GBS
Are you detail-oriented and experienced in compiling and publishing clinical... ...and compliance of regulatory submissions? We are looking for an Associate Clinical Safety Publisher to join our team at Novo Nordisk. If you...
...MIT World Peace University invites profiles for -
Job Description and Person Specifications:
Job Title - Associate Dean (Academic Monitoring)
Area - Administration
Location - Pune
Reporting Authority - Dean - Academics
Key Responsibilities
- Conduct...
...Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but... ...responsible for integrity, reliability, completeness and quality of clinical trial data and provides end to end clinical data management...
...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...
...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 pharmaceutical biotechnology and medical device customers a wide range of clinical development patient...
...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...
Rs 4 - 7 lakhs p.a.
...Call Monitoring FTE is responsible for assessing the performance of the customer service reps who deal with our client’s existing and potential... ...Mortgage Servicing ,Loan Origination
Designation: Process Associate- call monitoring
Vacancies: 1
Experience: 3.0 Year(s) - 5....
...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...
...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,... ...cranial nerve assessments, and motor/sensory evaluations, to monitor patient status and response to treatment.
Administer medications...
Rs 3 - 4 lakhs p.a.
...record
Generate the chart note
Job location New Mumbai
BAMS,MBBS,BDS,BUMS,BPT,ANY DOCTOR DEGREE
Designation: Vacancy for Doctors - Clinical Associate
Vacancies: 50
Experience: 0 - 4.0 Year(s)
Telephonic Interview scheduled. Apply now and attend interview....
...Job Description
Job Title: Clinical Information Science Associate Director Career Level - E
Introduction to Role:
Are you passionate about implementing technical solutions in the healthcare setting? Do you have a knack for leading and developing innovative solutions...
...includes the set up and execution of Central Monitoring and Data Analytics tool
Drive discussions with Global Clinical Operations, Data Strategy and Management, Stats... ...operational staff, such as the Clinical Research Associates (CRAs) / Senior CRAs (SCRAs), Local Study...
...Job Description
ROLE SUMMARY
As part of the Data Monitoring and Management group, an integral delivery unit within the Global Biometrics... ...timely and high quality data review and query management of clinical data supporting the Pfizer portfolio. The Data Manager executes...
...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...
...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....
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely... ....
2. Trial Execution : Conduct site initiation, monitoring, and close-out visits to ensure adherence to protocol, regulatory...
...Lead the development of the study specific eTMF plans for assigned clinical studies.
Perform quality control of documents submitted to... ...Essential Document Lists (EDLs) are maintained on an ongoing basis.
Monitor and identify study-specific eTMF trends and communicate to...
...years working experience in the Central Monitoring (RBM)
~ Experience in Oracle, PL/SQL, SAS... ...skills.
~ Working knowledge of clinical development process, understanding concepts... ...understanding key processes and principles associated with role including CRF design, database...
..."" Greetings From AGS Team"'
We are hiring for Process Associate / Sr. Associate (AML /KYC) - CHENNAI Location
If you are... ...experience is Mandatory in AML and KYC, CDD, EDD, Transaction Monitoring
Shift Timing 6 PM to 3 AM/Cab Facilities for both the way....
...Description
OBJECTIVES :
~ Perform monitoring and site management work to ensure that... ...to monitoring and study plan
Support clinical quality in managing CAPAs and other... ...clinical trials industry as Clinical Research Associate
Good working knowledge of GCP and...