Study Start Up Associate Ii

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.With our patients at the centre of all that we do, we help to accelerate the development...

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration,...

Centralized Study Associate II To complete Other duties/activities as assigned by study management team, but not limited to: Ø Manage clinical systems & access management Maintain study databases (CTMS, IWRS, EDC etc.) Support study team in eTMF management activities Support study team in data review and support activities. Support in generating the study...

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 access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

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 access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Follow all applicable departmental Standard Operating Procedures and Work Instructions.Complete required trainings according to required timelines.Complete day-to-day tasks ensuring quality and productivity.Maintain project and technical documentation in an appropriate manner.Perform checks to ensure quality of work completed.Ensure timely escalation as...

Centralized Study Associate I Manage study documents such as study level, country level and site level Maintain study databases (CTMS, IWRS, EDC etc.) Support study team in eTMF management activities Support study team in data review and support activities Upload, check, correct and maintain study documents for document review in the study eTMF regionally....

Brief Position Description:Supports the day-to-day operations of the data management projects, providing in-house data entry support to projects and administrative support to CDMs, according to GCDMP guidelines, local regulatory requirements, and Novotech/Client SOPs.Minimum Qualifications & Experience:Graduate in a clinical or life sciences related field....

At Premier Research, we help biotech and specialty pharma companies transform life-changing ideas into reality. What we do is profoundly connected to saving and improving lives, and we recognize our staff members are the most valuable asset in delivering success. Inspiring and nurturing staff to do their best work means a better, healthier future for all....

This is where you save and sustain livesAt Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.Baxter's products and therapies are found in almost...

NFTPL, based in Bangalore, a start-up and manufacturer of starch and derivatives, is setting up an inclusive R&D Lab. The preliminary R&D had been completed in association with a reputed and national level CSIR Institute. The Phase-II of the R&D will be both in-house and in collaboration with a premier research and knowledge institution. The incumbent will...

Job DescriptionTake your career to the next level and be involved in study startup processes in India. You will provide operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Office-based (Bangalore)You willDevelop site-specific startup timelines and meet the site activation targets Provide progress updates on...

Beckman Coulter Life Sciences' mission is to empower those seeking answers to life's most important scientific and healthcare questions. With a legacy spanning 80+ years, we have long been a trusted partner to our customers, who are working to transform science and healthcare with the next groundbreaking discovery. As part of our team of more than 2,900...

Service as Principal Investigator or Contributing Scientist for research studies under the direction of the Associate Director of the Pharmacokinetic group or a senior pharmacokineticist. Has overall responsibility for technical conduct of a study, review, documentation and reporting of results.A. Responsibilities/DutiesDesigns and reviews protocol, prepares...

Department – Finance GBS, MDMAbout the departmentGlobal Finance GBS Bangalore, established in 2007, supports Accounting, Finance & Procurement, Financial Planning & Analytics (FP&A) for Headquarters, Europe, North America, International Operations (IO) & GBS Bangalore, providing superior service and adding value through standardization and efficiency.The...

Position provides process, control, coordination, and approval of clinical trial documents. Position is responsible for ECD, Phase I-IV electronic trial master file (eTMF). Maintains an understanding of applicable regulatory requirements. Managing electronic Trial Master Files (eTMF), (Trial, Country and Site artifacts) for clinical studies in accordance...

When our values align, there's no limit to what we can achieve. Build Grant Estimate Timely preparation of accurate and competitive Clinical Study grants (Phases I – IV for all clinical indications) via proficient usage of any Clinical Study Pricing Tool that PAREXEL is required to use to support our Clients' needs. The default, currently...

Who we are:You Are:Associate II - Cloud Infrastructure ServicesThe Opportunity: Monitoring: Understand Priority and Severity based on ITIL practice. Understand agreed SLA with customer and adhere. Adhere to ITIL best practices Runbook Reference: Follow runbook for troubleshooting record troubleshooting steps and provide inputs for runbook changes. Use KB/SOP...

1. Protocol Familiarization : Learn to read and comprehend study protocols, sample analysis outlines, amendments, and study schedules, ensuring understanding of regulatory requirements and Labcorp SOPs/P&Ps relevant to client deliverables. 2. Data Analysis and Reporting : Performs initial review of bioanalytical data and originates noncompartmental...

1.Protocol Familiarization: Learn to read and comprehend study protocols, sample analysis outlines, amendments, and study schedules, ensuring understanding of regulatory requirements and Labcorp SOPs/P&Ps relevant to client deliverables.2.Data Analysis and Reporting: Performs initial review of bioanalytical data and originates noncompartmental analysis (NCA)...