Centralized Study Associate Ii

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...

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...

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,...

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...

ICON is looking for a Central Monitor to be based in Chennai. The Central Monitor is responsible for listing review and central data analysis to support quality and risk reviews of projects, by highlighting/escalating trends.Job ResponsibilitiesAs a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with...

Department – Centralised Monitoring Unit (CMU) Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career objectives? Then we might...

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...

Job OverviewProvide project related assistance to assigned project teams.; Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements.; Meeting quality and timeline metrics.;Essential Functions Complete appropriate rolespecific training to perform job duties.; Under...

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. Manage project and technical documentation in an appropriate manner. Provide administrative and technical support to internal departments and teams as...

Support the payment of assigned studies which could include study set-up, maintenance, timely and accurate payment to the sites, as well as issue resolution and study reconciliation. Provide excellent customer service and site issue resolution Review Electronic Data Capture updates and determine when certain budget items are payable Assist in setting...

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....

We're looking for people who are determined to make life better for people around the world. Purpose: The Clinical Data Management Associate is responsible for trial level clinical data execution including database structure, content and meaning, acquisition, validation, storage, retrieval, interchange, delivery and representation. This requires an in...

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....

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...

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...

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...

We are looking for Certified Employee Central (preferred) and Talent Management (Optional) practitioner in at least 1 implementations.Required Skills: Good knowledge around Process designs and Personas of SuccessFactors Employee Central Module. Strong configuration skills around Core EC functionalities like Business rules, MDF's and FO's, Associations,...

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...

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)...