Job Overview Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Clinical Lead is a member of the
Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site documents
IQVIA Biotech is hiring for Sr. Site Contracts Associate in Brazil with 5 years experience negotiating clinical site contracts and budget templates. IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25
IQVIA Biotech is seeking a Clinical Project Manager with at least 2 years experience in project management in Immuno-oncology and Cell & Gene Therapy. IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support
Internal Job Description Under moderate supervision, the Site Activation Specialist executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages
Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. The Contract Specialist is
IQVIA Biotech is seeking a Clinical Project Manager with at least 2 years experience in project management in Cardiovascular, Renal and/or Metabolic. IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across
Under moderate supervision, the Sr. Site Activation Specialist executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation;
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 navigate
City : Mohali State : Punjab (IN-PB) Country : India (IN) Requisition Number : 44589 Role Purpose Statement The overall responsibility of the Contract Admin Lead will be supervising the team for smooth execution and implementation
Every day, we get opportunities to make a positive impact – on our colleagues, partners, customers and society. Together, we’re pioneering the solutions of the future and unlocking the full potential of precious resources. Trusted to
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports).
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports).
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Clinical Trial Manager with focus on Project Management - Sponsor dedicated - Brazil Home Based Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
The International Trade Analyst supports Vertiv’s Global Supply Chain and Commercial Operations by managing import and export shipments via ocean, air, and ground transportation. Ensures compliance with trade regulations, accurate and timely shipment documentation, and effective
Overview You are expected to work closely with colleagues in research, marketing, technical, and other functions across all company locations. The role includes collaboration with academic and industry partners, close interaction with the sales and technical
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Senior CM Analyst II Join Us as a Senior CM Analyst II – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical
Head of AI Solutions Delivery About Andela Andela is transforming from a talent marketplace into an AI services leader, building a differentiated position at the intersection of elite technical talent and cutting-edge AI solutions. Were growing