Division Quality Department Formulation Sub Department 1 Formulation – Quality Control Job Purpose Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift. Key Accountabilities (1/6) Operate the equipment efficiently without error ...
Clinical Research Jobs Latest Articles
Clinical Research Assoc III
ClinicalresearchinfoHow you’ll spend your day Apply : https://careers.teva/job/Bangalore-Clinical-Research-Assoc-III-Indi-560064/1106363500/
Regulatory Affairs Associate I
ClinicalresearchinfoThe opportunity Regulatory Affairs associate I – RA publishing will participate in the publishing of different regulatory activities. The focus will be to ensure 100% quality and timeline of the submission. This role will be the primary interface with the ...
R&D Programmer I
ClinicalresearchinfoHow you’ll spend your day Apply : https://careers.teva/job/Navi-Mumbai-R&D-Programmer-I-Indi-400706/1093950200/
CANADA CRA Openings
ClinicalresearchinfoClinical Research Associate: https://careers.calian.com/careers/col-clinical-research-associate-3/ IQVIA CRA : https://jobs.iqvia.com/job/-/-/24443/57214210576?source=LinkedIn_Slots Clinical Research Associate II : https://jobs.smartrecruiters.com/PSICRO/743999948514253-clinical-research-associate-ii?trid=2d92f286-613b-4daf-9dfa-6340ffbecf73 Clinical Research Associate I/II Oncology – Toronto area : https://careers.iconplc.com/job/clinical-research-associate-i-ii-oncology-toronto-area-in-canada-jid-32731?_atxsrc=LinkedInSS&utm_source=LinkedInSS&apply%3Fsource=linkedin Sr CRA II : https://www.syneoshealth.com/clinical-corporate-careers/jobs/13686484-sr-cra-ii?src=JB-10120
US CRA Openings
ClinicalresearchinfoClinical Research Associate – Sponsor Dedicated : https://jobs.iqvia.com/job/-/-/24443/59833983264?source=LinkedIn_Slots Clinical Research Associate – CRA : https://careers.pipercompanies.com/details/113800/clinical_research_associate_cra AstraZeneca CRA : https://astrazeneca.wd3.myworkdayjobs.com/Careers/login?redirect=%2FCareers%2Fjob%2FUS%2FClinical-Research-Associate_R-188315-1%2Fapply%3Fsource%3DLinkedin Clinical Research Associate III : https://beigene.wd5.myworkdayjobs.com/BeiGene/job/Remote-US/Clinical-Research-Associate-III_R21869?source=Linkedin Medpace : https://careers.medpace.com/jobs/9313?mode=apply&iis=LinkedIn&lang=en-us
Junior Executive
ClinicalresearchinfoJob Purpose: Junior Executive (10-I) is to work as team member in SCP team. Key Responsibilities: • Sample preparation for NMR analysis• CMDD vial drop off• Sample submission for various analysis.• Weighing and recording the data.• Distribution of sample for registration.• Preparation ...
PRM Associate I
ClinicalresearchinfoJOB-DESCRIPTION • Recognize, exemplify and adhere to ICON’s values which center around our commitment to People, Clients and Performance.• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a ...
Lab Data Analyst I
ClinicalresearchinfoJOB-DESCRIPTION • Recognize, exemplify and adhere to ICON’s values which center around our commitment to People, Clients and Performance.• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a ...
Project Associate
ClinicalresearchinfoApply : https://careers.iconplc.com/job/project-associate-in-india-chennai-jid-32906
Site Initiation & Kit Inventory Coordinator Trainee
ClinicalresearchinfoPerforms main functions of Kit Inventory Center as needed, which includes but not limited to: ♦ Define and maintain the Kit Material Supply (KMS) system at project level according to Statement of Work (SOW) and/or at site level as necessary; ♦ Enter the ...
Clin Ops Specialist
ClinicalresearchinfoJob responsibilities• Responsible for performing activities in compliance with applicable Corporate and Clinical Operations Policies, Standard Operating Procedures and Work Instructions • Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, ...
Medical Writing Associate I
ClinicalresearchinfoLiterature search, preparation of Clinical study protocols and PSP according to required day to day Guidelines and Regulatory Requirements by using Product Monographs/Prescribing Information/Summary of Product Characteristics etc., as applicable.Preparation of Informed Consent Form/s (ICF) in line with Clinical study ...
Associate Medical Writer
ClinicalresearchinfoResponsible for preparing the narratives associated with the client’s/sponsor’s products from clinical trials for Clinical Study Reports (CSRs) or in order to support any health authority requests in accordance with regulatory and client’s/sponsor’s requirementsUnder departmental supervision, responsible for management of ...
Regulatory Affairs Associate
ClinicalresearchinfoBiologic/Small Molecules CMC 2 to 3 years of experience Supported the CMC activities related to Vaccine/Biologic/Small Molecules manufacturing and control including authoring of submission dossiers related to: – new application, post approval variations – Understanding of EU/CA/WHO/US regulations & guidance allowing appropriate review and compilation ...