Clinical Trials Jobs in Bogotá

Job Description#ONEGDMS Under the direction of the applicable management the Clinical Data Management Analyst is responsible for executing end to end data management activities pertaining to clinical trials including but not limited to; data management tool and system development validation and main...

Clinical Trials Regulatory Officer Maintenance AssociateHome-BasedMake an impact on patient health!The Global Site Activation unit within IQVIA has the vision to be the clear market leader in clinical trial site activation driving best in class employee site and customer experiences and industry-le...

We are looking for an experienced Translation Project Manager with expertise in linguistic validation and electronic Clinical Outcome Assessment (eCOA). This role manages the operational aspects of translation projects ensuring compliance with SOPs timelines and quality standards.Key Responsibilitie...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments...

About UsNu is one of the largest digital financial platforms in the world with more than 122 million customers across Brazil Mexico and Colombia. Guided by our mission to fight complexity and empower people we are redefining financial services in Latin America and this is still just the beginning of...

AECOM Enterprise Capabilities is seeking a talented and experienced Design Manager - Data Centers to be based in Bogotá Colombia office. The qualified candidate will oversee a wide variety of colocation and hyper-scale data center projects from site due diligence campus planning conceptual/schematic...

The Regulatory Support Associate plays a key role in supporting the regulatory and technical functions by ensuring accurate and timely management of regulatory data and documentation. This position involves coordinating admistrative functions of the regulatory and technical programs for the Cosmetic...

The Data Solution and Engineering team under Visa Consulting & analytics Data Science is a multidisciplinary group responsible for designing robust data infrastructures developing innovative machine learning solutions enforcing data governance standards and aligning machine learning projects with b...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. Youll lead with purpose breaking down barriers to innovation in a more connected compassionate world.A Day in the LifeThe Associate Regulatory Affairs Specialist p...

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments...

Software DeveloperLocation: Remote (Preference for candidates in or near U.S. Eastern Time)Employment Type: Full-TimeSalary Range: USD $3800 $4000 per monthAbout the RoleWe are seeking an experienced Software Developer with a strong focus on regression testing and validation to ensure the reliabili...

The TeamThe Government Affairs (GA) team shapes policy and regulation to drive business growth and advance Visas mission. As trusted advisors to governments and partners we secure our license to operate and build the innovative reliable and secure payments ecosystem that fuels global digital commerc...

Job DescriptionThe Medical Writing & Disclosure Department of the GCTO organization prepares a variety of regulated documentation in support of the clinical development portfolio and compliance in public disclosure of clinical trials and their results document disclosure and data sharing with extern...

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience we offer agile therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.IQVIA Biotech is seeking an experienced Clinical Project...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and...

Job DescriptionIntroducing Global Clinical Data Integration (GCDI): Transforming clinical data management in Latin America. With a focus on streamlining information our department collects cleans transforms and archives clinical data ensuring high quality and compliance. As a new addition to the reg...

Job DescriptionWith support of and/or CRA-Manager acts as primary site contact and site manager throughout all phases of a clinical research study taking responsibility of allocated sites. Develops strong site relationships and ensures continuity of site relationships through all phases of the tria...

JOB DESCRIPTION:About AbbottAbbott is a global healthcare leader creating breakthrough science to improve peoples health. Were always looking towards the future anticipating changes in medical science and technology.Working at AbbottAt Abbott you can do work that matters grow and learn care for yo...