Senior Clinical Research Associate job offers

CORE PURPOSE OF JOB The Department of Human Movement Science (HMS) invites applications for the position of Associate Professor or Senior lecturer. Situated in a modern, well-equipped facility, the department is home to three qualifications (i.e., BHSc in Biokinetics, Bachelor of Human Movement Science and Diploma in Sport Management) and two service units (i.e., Biokinetics and Sport Science Uni...

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 conducting operations in more than 90 cou...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

Associate Event/Project Manager page is loaded Associate Event/Project Manager Apply locations Athens, Greece Porto Salvo, Portugal Warsaw, Poland Cape Town, South Africa time type Full time posted on Posted Yesterday job requisition id R1400890 Job Title: Project Manager- Strategic Meetings and Events, EMEAContract: Fixed TermLocation: Greece, Portugal, Poland or South AfricaIQVIA is a leading g...

Associate Event/Project Manager page is loaded Associate Event/Project Manager Apply locations Athens, Greece Porto Salvo, Portugal Warsaw, Poland Cape Town, South Africa time type Full time posted on Posted Yesterday job requisition id R1400890 Job Title: Project Manager- Strategic Meetings and Events, EMEA Contract: Fixed Term Location: Greece, Portugal, Poland or South Africa IQVIA is a leadin...

Job Title: Project Manager- Strategic Meetings and Events, EMEAContract: Fixed TermLocation: Greece, Portugal, Poland or South AfricaIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries.IQVIA creates intelligent connecti...

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of $18 billion and approximately 55,000 employees in 50 countries. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics and increase laboratory pro...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Prepa...

These jobs were popular with other job seekers University of Pretoria Lecturer / Senior Lecturer / Associate Professor: Small Stock Flock Health (One Post) - Department of Production Animal Studies Permanent Full Time Published: 2 days ago Market Related EE/AA, Non EE/AA INTRODUCTIONFACULTY OF VETERINARY SCIENCEDEPARTMENT OF PRODUCTION ANIMAL STUDIESLECTURER/SENIOR LECTURER/ASSOCIATE PROFESSOR: S...

Senior Site Manager (Senior Clinical Research Associate) Location: Johannesburg, South Africa Johnson & Johnson Innovative Medicine is recruiting for a Senior Site Manager (Senior Clinical Research Associate) located within commutable distance of Johannesburg and with flexibility to travel. At Johnson & Johnson Innovative Medicine, what matters most is helping people live full and healthy lives. ...

Job Overview:This position is for an Associate Quality Assurance Director in the Risk Analytics team who will serve as the strategic quality engagement leader focusing on risk analysis projects and tracking for each business function with primary focus on Clinical Operations. The role includes the following activities:Responsibilities: Predominantly supports Clinical Operations globally. Provides...

Job Description The Associate Client Services Lead, under the supervision of senior members of Client Services team, serves as the main point of contact for their respective region's portfolio studies, manages the client / IQVIA PL relationship (as appropriate), oversee payment management projects and ensure sponsor satisfaction is achieved. Manage and oversee the initiation and study management ...

Main purpose of the job: Core responsibilities of the role will include database management, Extract, Transform, Load (ETL) operations, system design using tools like Power Automate and robotic process automation (RPA), supporting the senior management team, and utilizing strong data/statistical programming languages, Microsoft products, and REDCap Additionally, the role involves exploring cuttin...

Main purpose of the job:Core responsibilities of the role will include database management, Extract, Transform, Load (ETL) operations, system design using tools like Power Automate and robotic process automation (RPA), supporting the senior management team, and utilizing strong data/statistical programming languages, Microsoft products, and REDCapAdditionally, the role involves exploring cutting-...

CORE PURPOSE OF JOB The Department of Human Movement Science (HMS) invites applications for the position of Associate Professor or Senior lecturer. Situated in a modern, well-equipped facility, the department is home to three qualifications (i.e., BHSc in Biokinetics, Bachelor of Human Movement Science and Diploma in Sport Management) and two service units (i.e., Biokinetics and Sport Science Uni...

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 conducting operations in more than 90 cou...

Clinical Research Associate - Single Sponsor Dedicated page is loaded Clinical Research Associate - Single Sponsor Dedicated Apply locations Centurion, South Africa time type Full time posted on Posted 2 Days Ago job requisition id R1412219 Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study p...

Clinical Research Associate - Single Sponsor Dedicated page is loaded Clinical Research Associate - Single Sponsor Dedicated Apply locations Centurion, South Africa time type Full time posted on Posted 2 Days Ago job requisition id R1412219 Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study ...

When our values align, there's no limit to what we can achieve. Parexel is currently seeking Clinical Research Associates.Home-based in South Africa.Working as a Clinical Research Associate at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeli...

Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory r...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory...