Full Time Level: Mid Travel: Minimal Glassdoor Reviews and Company Rating Success Profile Check out the top traits we?re looking for and see if you have the right mix. Team player TechSavvy Communicator Proactive Detailoriented Analytical Rewards Global Impact We are one truly global team working together to propel each client?s journey ahead faster. Balance We value worklife balance. We try and
]Job Description The main objective of this role is to efficiently lead Project Team activities and actively participate in the planning and implementation of consistent Clinical Trial processes. You will: Coordinate and supervise Project Teams in APAC Monitor, collect and report project timelines, milestones, enrollment and general status for updates Direct communication with Global Project Mana
Ensures quality of the clinical monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and or tracking tools. May include the development of the Clinical Management Plan CMPSite Management Plan SMP.Interacts with the client and other functional departments related to clinical monitoring and site management activiti
EducationExperience: Master?s or bachelor?s degree in pharmacyLife Sciences with minimum 13 years of delivering end user training experience with at least one clinical application CTMS, eTMF or Safety database in a CROPharma company. 58 years of progressive clinical research experience. Responsibilities Ownership Serves as the primary trainer for clinical systems and deliver end user training o
Requirement & Qualification: Post Graduate degree in Pharmacy ChemistryQuality ControlPharmacokinetics or MSc Chemistry 1st Class Academic Record from a reputed college, with a Diploma in Clinical trials. The candidate should have strong quantitative and analytical skills. Heshe should have strong written and oral communication skills, with exposure to or basic understanding of clinical trials. Lo
JOB DESCRIPTION: Requirement & Qualification: Post Graduate degree in Pharmacy ChemistryQuality ControlPharmacokinetics or MSc Chemistry 1st Class Academic Record from a reputed college, with a Diploma in Clinical trials. The candidate should have strong quantitative and analytical skills. Heshe should have strong written and oral communication skills, with exposure to or basic understanding of cl
Job Overview: Global Specimen Solutions GSS is wholly owned company of Covance Inc., providing specialty services in the holistic specimen tracking space. GSS improves translational science through industry best practices and a uniquely powerful pipeline data management analytics solution. GSS reduces the time, cost and risk of specimen based research, while building robust, healthy data pipelines
Job Overview: Job Location: Bangalore; Contract Position for 6 months ? Follow applicable departmental Standard Operating Procedures and Work Instructions. ? Complete required trainings according to required timelines. ? Complete daytoday tasks ensuring quality and productivity. ? Maintain project and technical documentation in an appropriate manner. ? Perform checks to ensure quality of work comp
Qualifications A graduate degree or Post Graduate degreediploma preference in Health Science, Science, or Clinical is required.Good organizational, communication and computer skills required.Ability to exercise excellent attention to detail required.Ability to act independently and with initiative required to resolving problems.Medical terminology exposure preferred.Knowledge of operating procedure
Education : Any Medical Degree Professional Experience : 5 8 years of experience in Business Analyst & Design Job purpose ABK is looking for an individual with a background in Healthcare to join our Healthcare Information System Product Development. Knowledgeable in all aspects of designing and constructing healthcare business processes, functions and organizational structures. Understand business
Provide leadership to ensure the project or program is completed within budget, schedule and according to contract specifications. Ensure the projectprogram is progressing according to quality standards, SOPs, ICH andor other guidelines to fulfill regulations including oversight and maintenance of relevant data operations project documentation. Thorough knowledge of numerous EDC systems DataLabs,
Position: Associate Consultant Marketing and Sales Analytics Experience: 4y 5y Location: Bangalore Currently looking for candidates in Bangalore Joining: Immediate to 30 days if joining >30 days, resume will not be considered Responsibilities: a Provide consulting services to stakeholdersconsumers in the Marketing and Sales analytics space for US BU b Develop a good understanding of Marketi
The role of the Associate Clinical Data Coder ACDC is to perform assigned tasks or activities in clinical data coding. Activities may include coding of clinical data, generation, integration of queries, and running of reports under supervision of senior coding staff. All tasks should be performed in accordance to corporate quality standards, SOPsWork InstructionGuidelines, ICHGCP andor other intern
Job Summary: Assistant Data Manager for Global Specimen Solutions is responsible and accountable to deliver tasks according to procedural requirements and agreed upon service levels of Global Specimen Solutions for Covance Central Laboratory Services. Work with the internal DM leads to coordinate and fulfill requests related to protocolspecific data management requirements. Lead and support Data Ma
Job Description The main objective of this role is to efficiently lead Project Team activities and actively participate in the planning and implementation of consistent Clinical Trial processes. You will: Coordinate and supervise Project Teams in APAC Monitor, collect and report project timelines, milestones, enrollment and general status for updates Direct communication with Global Project Manag
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