Empleos de Fortrea en Colombia

· Perform the role of the Lead Statistical Programmer. · Plan, execute and oversee all programming activities on a study. · Develop and maintain SAS programs to create SDTM and ADaM datasets · ...

Develops, reviews and finalizes clinical trial documents such as informed consent forms. Applies knowledge of GCP Guidelines to review and develop Informed Consent Forms (ICF). Ensures that research participants can easily understand the content of the consent form. · ...

Perform and coordinate a variety of tasks to support the company as part of the leadership of the office service team. · ...

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. · ...

AsaSenaororPrincipalStatisticalProgrammerinoursponsor-dedicatedFlexibleSolutionsbusinessunit,youwillbecentraltothesuccessfuldeliveryofcomplexglobaloncologyclinicaltrials(PhasesI–III)for some of the world's most renowned and innovative pharmaceutical companies. · ...

Job Description · The role involves developing, reviewing, finalizing, and maintaining clinical trial documents such as informed consent forms. · Develop ICFs by applying knowledge of GCP Guidelines, regulatory requirements, privacy standards, biological samples standards, therap ...

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex global oncology clinical trials (Phases I–III) for some of the world's most renowned and innovative pharmaceutical ...

Perform the role of the Lead Statistical Programmer. · Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other departments and the client etc. ...

Perform and coordinate a variety of tasks to support the company. · ...

Tasks: · Responsible for developing, reviewing, finalizing, and maintaining clinical trial documents such as informed consent forms. · Applies knowledge of GCP Guidelines, regulatory requirements, regulatory framework of privacy standards and biological samples standards, therape ...

Summary Of Responsibilities · Perform the role of the Lead Statistical Programmer. · Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing quality, · interaction wit ...

Perform and coordinate a variety of tasks to support the company as part of the leadership of the office service team. · ...