Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Summarized Purpose: Provides medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor
Deadline for Applications June 14, 2026 Hardship Level A (least hardship) Family Type Family Residential location (if applicable) Grade GS7 Staff Member / Affiliate Type General Service ReasonRegular Regular Assignment Target Start Date 2026-04-23 Standard Job
Deadline for Applications June 15, 2026 Hardship Level A (least hardship) Family Type Family Residential location (if applicable) Grade GS7 Staff Member / Affiliate Type General Service ReasonRegular Regular Assignment Target Start Date 2026-08-03 Standard Job
JOB DETAILS Type of contract : Consultant Contract Level : Level 2 - Middle Hiring Unit : Social and Human Sciences Sector (SHS) Duty Station : Mexico City Work location : On site Duration of contract : 6 months
Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time
Site Name : Poznan Grunwaldzka, Bengaluru Luxor North Tower, Egypt - Cairo, Mexico City Torre Mitikah, Mississauga Milverton Drive Posted Date : Feb CTA/IND Submission lead-Submission Delivery Excellence-Investigational , position holder(s) will be accountable for Regulatory Submission
Descripción y detalle de las actividades Monitor inventory levels and ensure accuracy through regular audits and cycle counts, cooordinate with the contract manufacturer to optimize inventory processes and resolve discrepancies, implement inventory control procedures to minimize stockouts
Descripción y detalle de las actividades Monitor inventory levels and ensure accuracy through regular audits and cycle counts, cooordinate with the contract manufacturer to optimize inventory processes and resolve discrepancies, implement inventory control procedures to minimize stockouts
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
Job Purpose Its purpose is to plan the contract manufacturing production programs, ensuring that the sites volumes are met; it places purchase orders for raw materials with the subsidiary to meet production demand. It communicates and proposes
Education and Experience : - Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) in the industry; Or - Direct experience in safety/Pharmacovigilance (comparable to 2
Asphalion is growing and we are looking for a Regulatory Affairs Consultant / Senior Consultant to join our CMC unit of consultants for the pharmaceutical industry ! Someone who loves to take on new challenges, to
General Information File N° Date 16/04/24 Department Administracion Area NAPS JRZ Administracion Requested Position Administrative Assistant Vacancies 1 General functions 1. Elaboración de nómina (NAPS Juarez Admón. y Specialized HR) - Altas, bajas y captura de
Job Overview : Summary of Responsibilities : - Maintain awareness of regulatory legislation, guidance, and practice in the assigned countries. - Compile and prepare routine submission filed to IRB/IEC/Third body/Regulatory Authorities (e.g., INDs/CTAs) and liaise with them
Translate deep regulated-pharma expertise into AI that validates biopharma workflows. Aumente sus posibilidades de llegar a la fase de entrevista leyendo la descripción completa del puesto y enviando su solicitud sin demora. ■ Company Overview Cheiron
Translate deep regulated-pharma expertise into AI that validates biopharma workflows. Aumente sus posibilidades de llegar a la fase de entrevista leyendo la descripción completa del puesto y enviando su solicitud sin demora. ■ Company Overview Cheiron
Asphalion is growing and we are looking for a Regulatory Affairs Consultant / Senior Consultant to join our CMC unit of consultants for the pharmaceutical industry ! Someone who loves to take on new challenges, to
In a nutshell Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Asegúrese de enviar su solicitud rápidamente para maximizar sus posibilidades de ser considerado para una entrevista.
About The Role Develops and executes overall Clinical Pharmacology scientific strategies for assigned Therapeutic Area (TA). Oversees all aspects of Clinical Pharmacology activities for assigned clinical development compounds.Serves as a key member of clinical protocol development
Pharmacovigilance Associate - Mexico, Mexico City ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on