Associate Study Coordinator

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)...

1. Data Analysis and Reporting : Performs initial review of bioanalytical data and originates noncompartmental analysis (NCA) using Phoenix WinNonlin in support of pharmacokinetic and toxicokinetic studies. Aids in report preparation, including tables and figures. 2. Study Conduct: Serves as the primary contact for communication and interaction with...

1.Data Analysis and Reporting: Performs initial review of bioanalytical data and originates noncompartmental analysis (NCA) using Phoenix WinNonlin in support of pharmacokinetic and toxicokinetic studies. Aids in report preparation, including tables and figures.2.Study Conduct:Serves as the primary contact for communication and interaction with other...

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,...

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...

Site Name: Bengaluru Luxor North TowerPosted Date: Jul Competencies Performance Document management, business communication, quick learning abilities, data entry and review, exposure to pharma domain Trust Communication with Impact, Collaborative working, influencing, stakeholder engagement Culture GSK culture, accountability, teamworkPurpose:VEO Study...

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...

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...

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...

62584BRTitle:System Studies Engineer SeniorJob Description:Quest Global is an organization at the forefront of innovation and one of the world's fastest growing engineering services firms with deep domain knowledge and recognized expertise in the top OEMs across seven industries. We are a twenty-five-year-old company on a journey to becoming a centenary one,...

62584BRTitle:System Studies Engineer SeniorJob Description:Quest Global is an organization at the forefront of innovation and one of the world's fastest growing engineering services firms with deep domain knowledge and recognized expertise in the top OEMs across seven industries. We are a twenty-five-year-old company on a journey to becoming a centenary one,...

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,...

CMR University offers an outstanding and comprehensive array of academic programmes, and at the core of our wide range of academic inquiry is the commitment to attract and engage the best minds in pursuit of greater human understanding, pioneering new discoveries, and service to society. If you are a motivated academic or research professional ready to make...

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....

Company DescriptionWe are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2, 700 driven, dedicated, and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Company DescriptionWe are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2, 700 driven, dedicated, and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

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...

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...

Job Title: Associate Director - Study Data ManagerCareer Level - EIntroduction to the Role:Are you prepared to elevate our leading Oncology pipeline to the next level? As the Associate Director - Study Data Manager, you will be in charge of coordinating the Clinical Data Management (CDM) deliverables on assigned clinical studies. You will play a key role in...