ich jobs in Calgary

MMS is a data-focused CRO delivering regulatory and clinical writing support across pharmaceutical, biotech, and medical device sectors. The Medical Writer will critically evaluate literature, write and edit pivotal regulatory documents, and mentor junior writers to ensure high-quality submissions. Responsibilities include managing timelines, coordinating...

MMS is a data-focused CRO delivering regulatory and clinical writing support across pharmaceutical, biotech, and medical device sectors. The Medical Writer will critically evaluate literature, write and edit pivotal regulatory documents, and mentor junior writers to ensure high-quality submissions. Responsibilities include managing timelines, coordinating...

Principal Medical WriterThe Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with...

MMS is a data-focused CRO delivering regulatory and clinical writing support across pharmaceutical, biotech, and medical device sectors. The Medical Writer will critically evaluate literature, write and edit pivotal regulatory documents, and mentor junior writers to ensure high-quality submissions. Responsibilities include managing timelines, coordinating...

Manage Canadian clinical trial start-up submissions using Health Canada knowledge and precise regulatory documentation from a remote position. Coordinate approvals and timelines for Premier Research projects. As a Site Start-up Associate II, you support Premier Research's Clinical Monitoring, Site Management and SSU team. You prepare Central and Local EC...

Surveillez des essais cliniques en oncologie pour IQVIA depuis votre domicile dans l'est du Canada, en français et en anglais. Comme attaché de recherche clinique II expérimenté, vous assurez la conformité des essais de phase I à IV aux protocoles, aux BPC/ICH et aux exigences réglementaires. Vous gérez les activités des sites du démarrage à la...

Lead clinical medical writing remotely from Ontario, applying regulatory expertise and scientific communication skills to complex study deliverables. Collaborate across Syneos Health teams.As a Senior Medical Writer, you will manage writing activities for individual studies with minimal supervision. You will prepare clinical documents, review statistical...

Surveillez des essais cliniques en oncologie pour IQVIA depuis votre domicile dans l’est du Canada, en français et en anglais.Comme attaché de recherche clinique II expérimenté, vous assurez la conformité des essais de phase I à IV aux protocoles, aux BPC/ICH et aux exigences réglementaires. Vous gérez les activités des sites du démarrage à la...

Manage Canadian clinical trial start-up submissions using Health Canada knowledge and precise regulatory documentation from a remote position. Coordinate approvals and timelines for Premier Research projects.As a Site Start-up Associate II, you support Premier Research’s Clinical Monitoring, Site Management and SSU team. You prepare Central and Local EC or...

Attaché de recherche clinique II IQVIA est à la recherche d'un ARC II expérimenté en surveillance d'essais cliniques en oncologie. Ce poste, basé à domicile dans l'est du Canada, nécessite la maîtrise du français et de l'anglais. Aperçu du poste L'ARC II est responsable de la surveillance des essais cliniques de phase I à IV afin d'assurer la...

## Senior Clinical Research Associate (Canada)Apply: Remote: Canada: Part time: Posted 18 Days Ago: R6995Premier Research is looking for a Senior Clinical Research Associate (Canada) to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into...

Attaché de recherche clinique II IQVIA est à la recherche d'un ARC II expérimenté en surveillance d'essais cliniques en oncologie. Ce poste, basé à domicile dans l'est du Canada, nécessite la maîtrise du français et de l'anglais. Aperçu du poste L'ARC II est responsable de la surveillance des essais cliniques de phase I à IV afin d'assurer la...

## Drug Safety AssociateApply: Remote, ON: Full time: Posted Today: R2617957Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our...

## Drug Safety AssociateApply: Remote, ON: Full time: Posted Today: R2617957Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with...

## Site Start up Associate II (Canada Regulatory Affairs)Apply: Remote: Canada: Full time: Posted 11 Days Ago: R6981Premier Research is looking for a Site Start up Associate II (Canada Regulatory Affairs) to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing...

About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating. About MMS MMS is an innovative,...

Principal Medical Writer The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of the position are organizing, analyzing, interpreting, and presenting scientific and statistical information in accordance with...

# Drug Safety AssociatePostuler: Remote, ON: Temps Plein: Publié aujourd'hui: R2617957**À propos de Cencora**Cherchez-vous à faire une différence dans la vie d’un patient? Chez AmerisourceBergen, vous trouverez une culture innovante et collaborative, axée sur le patient et soucieuse de faire la différence. En tant qu’organisation nous sommes unis...

# Drug Safety AssociatePostuler: Remote, ON: Temps Plein: Publié aujourd'hui: R2617957**À propos de Cencora**Cherchez-vous à faire une différence dans la vie d’un patient? Chez AmerisourceBergen, vous trouverez une culture innovante et collaborative, axée sur le patient et soucieuse de faire la différence. En tant qu’organisation nous sommes unis...