Clinical Research Co-ordinator

Kickstart your career inClinical Researchwith us We atS3 Clinical Researchare looking for02 passionate internsinAhmedabadfor aGlobal Clinical Trialproject. What's in it for you? 6-month (180 days) structured internship Internship Certificate to boost your profile Incentive for top performers Best performers will behired as CRCat S3 Clinical ResearchThis is...

S3 Clinical Research is expanding, and we are looking for adedicated Phlebotomistto join our team. Position:Phlebotomist Organization:S3 Clinical Research - Clinical Lab Vertical Location:Ahmedabad Joining:ImmediateKey Responsibilities:Collecting and handling blood samples with precision and care.Maintaining proper labeling, documentation, and storage of...

PRINCIPAL DUTIES AND RESPONSIBILITIES:Note: These statements reflect the general description of the position and are not intended to be an all-inclusive list of task to which the employee may be assigned.A. Co-ordinate with CDCs, database programmers and other study team members on study progress.B. Identify resource for the project and to manage resource...

About the Role:Key role as a project manager would be Single Point of Contact (SPOC) for the Sponsor from Sterling Accuris Wellness Pvt. Ltd. for laboratory testing and the associate services for clinical trials.The role will require the ability to support the clinical trial study pipeline which could include various projects covering various therapeutic...

Company DescriptionHREE Research Pvt. Ltd. is a full-service Clinical Research Organization (CRO) offering comprehensive, end-to-end clinical research solutions. We specialize in supporting pharmaceutical, biotechnology, and medical device companies across all phases of clinical trials. Our services include study design and protocol development, regulatory...

Coordinate day-to-day activities of clinical trials from initiation to close-out. Recruit, screen, and enroll eligible participants as per study protocol. Schedule and conduct study visits, ensuring adherence to study timelines. Maintain accurate and timely documentation including case report forms (CRFs), informed consent forms (ICFs), and other...

Overseeing the trouble-free running of clinical trialsCollecting data obtained from research, coding and analyzing itManaging budgets set aside for researchCommunicating with participants regarding study objectivesAdministering questionnaires and monitoring participants to ensure they adhere to the studys rulesLiaising with laboratories regarding research...

Dear Candidate,Below are the Job Details for Clinical SAS Programmer role at CBCC Global Research LLP.Candidate should have the exposure of SDTM, ADAM and TLF.Job Location : Ahmedabad At OfficePosition : 2Experience: 2-5 years in CRO preferred / Pharma industryQualification : M. Sc. Statistics/Any Science GraduateMandatory experience in Clinical...

Role & responsibilitiesEC Submission• To get the documents from Central Drive, print, prepare files accordingly, and dispatch them to the respective sites prior to the Ethics Committee meeting conducted at site.SIV (Site Initiation Visit) Kits Preparation• To co-ordinate with CRD and prepare the SIV kits, study related material (NS Bottle, Syringe &...

Role & responsibilitiesPrepare clinical study report of BABE studies and patient based clinical trial studies (PK end point/PD end point/clinical end point studies) on the basis of data received from clinic after completion of study as per regulatory requirement/SOPs/client standards/client approved templates.Final compilation of the project report with...