Overview
Physician, Medical Specialist Jobs in Montréal – Quebec at Syneos Health
Title: Physician, Medical Specialist
Company: Syneos Health
Location: Montréal – Quebec
Category: Healthcare
Description
Physician – Contractor – Canada
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 realities.
Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.
Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.
Discover what our 29,000 employees, across 110 countries already know:
WORK HERE MATTERS EVERYWHERE
Why Syneos Health
We are passionate about developing our people, through
career development
and progression; supportive and engaged line management; technical and therapeutic area training; peer
recognition
and total rewards program.
We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together
diversity
of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
Job responsibilities
Primary Function
The physician works closely with the qualified investigator to manage and oversee subject safety during screening, during the conduct of clinical studies and for the post-study follow up of Bioequivalence and Phase 1 clinical trials in compliance with
clinical research
regulations.
Major
Responsibilities
Ensure subject safety at all times during the clinical study and after the study has been completed as required by the protocol and GCP and GLP regulations.
Review study protocols to acquire in-depth knowledge of the protocol.
Assist the Qualified Investigator in all duties regarding the safe conduct of
clinical research
.
Carry out the full spectrum of medical activities related to subject eligibility for studies (medical exam, laboratory results, electrocardiogram assessment…) so that
inclusion
and exclusion criteria are respected (pre-study).
Perform follow-up and ensure the quality of information related to subject eligibility.
Responsible for on-study supervision and works closely with
clinical research
staff.
Perform all required clinical exams as per the study protocol.
Assess adverse events and carry out the appropriate medical judgement and follows-up to determine the resolution of adverse events.
Interact with clients for onsite visits to address any safety concerns/questions.
Participate in on-call coverage requirements.
May be called upon to perform other duties as required.
May be assigned other clinical tasks.
Responsible for performing activities that are in compliance with applicable Corp…
