The Upper Shelf - Toronto, Ontario

Join our warehouse team in sorting donations coming from the community, which are distributed on our MJRH outreach van. · ...

We are seeking a highly skilled Lead Clinical Programmer to join our sponsor dedicated team at Fortrea, a leading global contract research organization (CRO). · The successful candidate will have extensive experience in data management and/or database programming activities inclu ...

We are seeking a Senior Data Manager to take leadership in client-facing activities along with on studies. · Lead studies including (but not limited to) a combination of healthy volunteer and patient populations, multi-site, complex protocol design, strong client management requi ...

This job is with Thermo Fisher Scientific and involves providing medical oversight of clinical trials to ensure company SOPs are followed. The associate medical director will attend and present at investigator and sponsor meetings, provide medical consultation to clients and proj ...

We are seeking Experienced Clinical Research Associates (CRAs) to lead and support our Full Service Outsourcing team. · Oncology or Ophthalmology desired. · ...

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. · CAR-T experienced Sr. CRAs located anywhere in Canada strongly desired**What You Will DoYou will utilize your skills, knowledge, and clinical judgement t ...

Joining Fortrea's SAS Programming team of data management sponsor dedicated team will offer a rewarding career, a chance to work in an energetic & team-oriented workplace and exposure within a world-leading team. · ...

As an experienced Principal Biostatistician in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials for renowned, innovative and global top pharmaceutical and biotech companies. · ...

We are seeking a Senior Clinical Data Manager to take leadership in client-facing activities along with on studies.This individual will take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes ass ...

The Associate Medical Director will provide medical oversight of clinical trials to ensure company SOPs are followed. · Maintains adherence to applicable regulations and ICH guidelines regarding clinical trials. · Ensures tasks delegated to pharmacovigilance are properly executed ...

This job provides medical oversight of clinical trials to ensure company SOPs and regulatory requirements are followed. · ...

Provides medical oversight of clinical trials to ensure company SOPs. Attends and presents at investigator and sponsor meetings. · Suitable clinical trial experience in a Contract Research Organization or pharmaceutical company. · ...

We help bring life-changing treatments to patients faster. We are seeking an experienced Senior Regulatory Medical Writer to lead the development of high-complexity clinical regulatory documents in partnership with a leading global pharmaceutical company. · You can shape your car ...

Lead authoring and development of high- complexity clinical regulatory documents for a Top 10 global pharmaceutical company as an embedded member of their team. · ...