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4.0 - 8.0 years
0 Lacs
rajasthan
On-site
As a Site Activation Specialist II at Syneos Health, you will be responsible for ensuring quality deliverables at the country level while following project requirements and applicable country rules under moderate oversight from the SSU Country Manager. You will work within forecasted submission/approval timelines, track milestone progress in the SSU tracking system, and investigate any delays with clear rationale and contingency plans as needed. Additionally, you will monitor basic financial aspects of the project, review and comply with Standard Operating Procedures (SOPs) and Work Instructions (WI), and support the continuous improvement of quality in all Site Start-Up (SSU) components. Yo...
Posted 3 months ago
3.0 - 7.0 years
0 Lacs
karnataka
On-site
About ProcDNA: ProcDNA is a global rocket ship in life sciences consulting. We fuse design thinking with cutting-edge tech to create game-changing Commercial Analytics and Technology solutions for our clients. We're a passionate team of 300+ across 6 offices, all growing and learning together since our launch during the pandemic. Here, you won't be stuck in a cubicle - you'll be out in the open water, shaping the future with brilliant minds. Ready to join our epic growth journey We are currently seeking a Programmer Analyst with a strong hands-on experience in EDC platforms such as Medidata RAVE, InForm, Central Designer, or Veeva Studio. The ideal candidate will possess a solid understandin...
Posted 4 months ago
3.0 - 7.0 years
0 Lacs
haryana
On-site
As a Safety & Pharmacovigilance Specialist I at Syneos Health, you will play a crucial role in ensuring the safety and well-being of patients involved in clinical trials and post-marketing programs. Your responsibilities will include entering information into PVG quality and tracking systems, processing ICSRs according to SOPs, and evaluating ICSR data for completeness and accuracy. You will be responsible for triaging ICSRs, entering data into safety databases, coding events, medical history, and concomitant medications, as well as compiling complete narrative summaries. Additionally, you will be involved in identifying information to be queried, following up until resolution, and generatin...
Posted 4 months ago
2.0 - 6.0 years
0 Lacs
pune, maharashtra
On-site
As a Clinical Research Associate (CRA), you will play a key role in conducting Phase I-IV clinical BA/BE studies. Your primary responsibilities will involve monitoring and managing activities at clinical sites to ensure that project timelines and deliverables are achieved. Building strong relationships with clinical sites and investigators will be essential, along with assessing protocol and regulatory compliance based on local and federal requirements, ICH GCP guidelines, and PSI SOPs. Your focus will be on safeguarding subjects" rights, safety, and well-being, as well as maintaining data quality. Your tasks will include preparing, conducting, and reporting on various activities such as sit...
Posted 4 months ago
1.0 - 5.0 years
0 Lacs
karnataka
On-site
Excelya is a leading independent Contract Research Organization (CRO) in Europe, dedicated to providing a people-centered approach since its inception in 2014. As a part of the ambitious health company, with a team of 900 Excelyates, our unique service model offers a diverse array of projects, enabling professional growth and personal development. In collaboration with experts, Excelya aims to advance scientific knowledge and enhance the patient journey, striving to become the clinical research leader in Europe. As a Clinical Data Manager at Excelya, you will be responsible for executing Data Management tasks in compliance with regulatory standards and Client SOPs. Working under the supervis...
Posted 5 months ago
10.0 - 12.0 years
1 - 6 Lacs
Bengaluru
Work from Office
Data Management Manager Location: Bangalore Experience: 10+ years Education: Science Graduate Notice Period: Immediate Joiners preferred Skills: Data management, Line management, ICH GCP, data management FSP, clinical study, QC,
Posted 6 months ago
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