Biometric Program Lead

When our values align, there's no limit to what we can achieve.This role can be flexibly based in select EMEA locations.Picture Yourself At Parexel :The Associate Global Biometrics Delivery Lead (ADL), reporting into the Global Biometrics Account lead (GBAL) or Global Biometrics Group Lead (GBGL), works under the guidance of an experienced Biometrics...

Parexel is seeking an experienced Global Biometrics Delivery Director to lead our biometric program team. The successful candidate will have several years of experience in clinical research within a CRO, Pharma, or Biotech environment.As a key member of the leadership team, you will provide overall leadership and management for database programming, data...

About the JobWe are seeking an experienced Global Biometrics Delivery Specialist to join our team. The successful candidate will provide overall leadership and management for database programming, data integration, data management, and statistical services on a project or program.Key Responsibilities:Effectively communicate with internal and external...

Are you passionate about advancing the field of clinical trial statistical analysis? Do you want to work on global projects across therapeutic areas?We are looking for a skilled Clinical Study Report Developer to join our team at IQVIA.As a Clinical Study Report Developer, you will be responsible for developing high-quality clinical study reports using...

Job DescriptionThis Associate Director Data Operations position is an excellent opportunity for a skilled professional to lead our global biometrics delivery team. As a key member of the team, you will be responsible for providing overall leadership and management for database programming, data integration, data management, and statistical services on a...

About the RoleThis exciting opportunity is for a skilled Clinical Research Project Manager to join our team. As a key member of the global biometrics delivery team, you will be responsible for providing overall leadership and management for database programming, data integration, data management, and statistical services on a project or program.Key...

About the OpportunityThis Senior Clinical Trial Coordinator role offers an exciting opportunity to work on innovative projects at the forefront of the industry. As a key member of the global biometrics delivery team, you will be responsible for providing overall leadership and management for database programming, data integration, data management, and...

Requirements:Degree in Engineering: A degree in Engineering is required for this role.Factory Experience: The successful candidate must have at least 2 years of experience in a factory setting.Continuous Improvement Experience: Strong practical experience in leading and coaching Continuous Improvement programs, preferably experienced in several...

MMS Holdings Inc. is an award-winning, data-focused clinical research organization (CRO) that supports the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges.We are seeking a highly skilled Senior Statistical Programmer to join our team. The ideal candidate...

Do you want to make a meaningful difference in the lives of patients and populations worldwide?We are seeking a talented Statistical Programming Lead to join our team at IQVIA.As a Statistical Programming Lead, you will be responsible for leading a team of statistical programmers in developing high-quality clinical study reports using advanced statistical...

ResponsibilitiesServe as primary point of contact for customer on data management deliverablesManage multiple large studies or program of studies (possibly global)Provide leadership and senior support to DTLs on multiple large global programs of global studiesProvide project management expertise working with customer data managers, key decision makers, and...

IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home...

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.We are seeking an experienced Statistical Programmer to join our team in developing clinical study report materials using SAS programming language.The successful candidate will utilize their...

MMS Holdings Inc. is committed to delivering exceptional results in clinical research. Our team of experts supports the pharmaceutical, biotech, and medical device industries with our cutting-edge approach to complex trial data and regulatory submission challenges.We are seeking a highly skilled Senior Statistical Programmer to lead our data science efforts....

When our values align, there's no limit to what we can achieve.Parexel is currently seeking a Senior Statistical Programmer to join us in South Africa, dedicated to a single sponsor.Picture Yourself At Parexel :The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in...

About the Role:We are seeking a highly motivated and experienced Wellness Centre Manager to lead our student services team. The successful candidate will have a strong background in clinical psychology and experience in managing student wellbeing programs.Key Responsibilities:Develop and implement policies and procedures to ensure that student wellbeing...

Job title : Assistant Director: Residence Life and College CommunitiesJob Location : Free State, BloemfonteinDeadline : April 28, 2025Quick Recommended LinksJobs by Location Job by industries Duties and responsibilities Residence operational management:Ensure effective management of residence life operations at the campus's residence of UFS Lead the...

Parexel is a leading clinical research organization that supports studies across various therapeutic areas. As a Clinical Programmer, you will be part of our team dedicated to delivering high-quality data review and trial management services.This role requires the provision of data review and trial management deliverables for multiple compounds and trials....

The suitable candidates main responsibilities and duties include, but are not limited to the following: Key Controller Duties & ResponsibilitiesAccurate input into the ICrypto vetting system.Preparing documentation as required for ON Boarding and Offboarding of individuals on ICrypto.Submit ICrypto application documents to the vetting team for uploading...

Eduvos invites applications for a Part-Time Lecturer position in Information Technology.This role involves delivering lectures, leading tutorials, and assessing student performance.The ideal candidate will possess strong teaching skills, excellent communication abilities, and a passion for education.Design and implement engaging lesson plans.Provide...