CRA II (Location: Sao Paulo) Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them
CRA II - SR CRA Brazil Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market
Company Description PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials
Clinical Trial Manager I with some experience in project management as a CTM or PM - Sao Paulo, Brazil Client Based (50% of the time in clients office) Syneos Health® is a leading fully-integrated life sciences
Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions • Assist Clinical Research Associates (CRAs) and
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,
In line with the Marketing department strategy, the Senior Marketing Analyst provides support to all Social Media activities in Brazil such as content, images and video production with the support of a digital marketing agency, community
Clinical Trials Assistant I Hybrid Role - Location: São Paulo, Brazil Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial
Job Title : TMF Associate Employment Type :Full time, Permanent Job Reports To : Manager, TMF Operations Department/Unit Name : TMF Operations Job Summary : Responsible for the management of the Trial Master File (TMF) content and
Work Schedule Standard (Mon-Fri) Environmental Conditions Office At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our
Remarks : The salary range stated is the basic salary. After three rounds of interviews, the specific salary will be determined based on your interview performance and previous salary level. Core Requirements : Chinese in Brazil,
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Clinical Team Manager PPD’s (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life saved.
Clinical Research & Technical Associate (CRA / CTA) Lea el resumen de esta oportunidad para comprender qué habilidades, incluidas las habilidades interpersonales relevantes y el dominio de paquetes de software, se requieren. Position Overview We are
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Join Us as a Sr Clinical Trial Manager - Make an Impact at the Forefront of Innovation The Clinical Trial Manager is accountable for achieving the final clinical deliverable
The Regulatory Affairs Associate will support the preparation, tracking, and coordination of Ethics Committee (EC) and Regulatory Authority (RA) submissions. Under supervision, the Associate will assist the Regulatory Affairs team in ensuring that clinical trial submissions
Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate
We’re expanding our capabilities across Latin America , and we’re hiring a Senior Clinical Research Associate to support critical studies across Brazil ! Responsibilities Independently oversees all aspects of study site management to ensure patient safety
Sr. CRA I (Sponsor dedicated) - Sao Paulo, Brazil Home Based Senior Clinical Research Associate dedicated to sponsor activities; responsible for site qualifications, monitoring, and close‑out visits in both on‑site and remote settings. Job Responsibilities Perform
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description PPD’s (a part of Thermo Fisher Scientific) mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it’s
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Trial Manager - Make an Impact at the Forefront of Innovation The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually