Instagram
youtube
Facebook

Physician - Clinical Research (Quebec City)

0-2 year years
Not Disclosed
10 Feb. 7, 2025
Job Description
Job Type: Remote Education: Certification in Advanced Cardiac Life Support (ACLS) or equivalent; must be certified or recertified to oversee study monitoring or have documented equivalent experience Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About Syneos Health

Over the past five years, we have collaborated with 94% of all newly FDA-approved drugs and 95% of EMA-authorized products. We have participated in over 200 studies across 73,000 sites, involving more than 675,000 trial patients.

At Syneos Health, you will take the initiative and challenge the status quo in a highly competitive and ever-evolving environment. Syneos Health is the only fully integrated biopharmaceutical solutions organization specifically designed to accelerate customer success. Our approach seamlessly integrates capabilities to provide valuable insights that help therapies reach patients faster and assist clients in achieving their goals.

Our success is driven by collaboration, with every team member excelling in their respective fields. We bring together a diverse pool of talented experts who provide critical services to support our organization. Every role is essential in advancing our vision of shortening the distance from science to life (Shortening the Distance from Lab to Life®).

Why Choose Syneos Health?

  • We prioritize the growth and development of our employees through career advancement, professional training, technical and therapeutic area education, peer recognition programs, and rewards.

  • We are committed to fostering a Total Self Culture, where employees can be their authentic selves. Our culture unites us globally, and we prioritize the well-being of our employees.

  • We strive to build an organization where people are eager to work, and our clients want to partner with us. By bringing together diverse perspectives, backgrounds, and experiences, we create an environment where everyone feels valued.


Position Overview

The Physician works closely with the Qualified Investigator to manage and monitor subject safety during screening, clinical trial execution, and post-study follow-up for bioequivalence and Phase 1 clinical trials. The role ensures compliance with clinical research regulations.

Key Responsibilities

  • Ensure the safety of study subjects at all times during and post-study, as outlined in the protocol, Good Clinical Practices (GCP), and Good Laboratory Practices (GLP) regulations.

  • Review study protocols for a comprehensive understanding of study procedures.

  • Assist the Qualified Investigator in all tasks related to the proper execution of clinical research.

  • Conduct medical activities related to subject eligibility, including medical exams, laboratory results assessment, and ECG evaluations, ensuring inclusion/exclusion criteria are met (pre-study phase).

  • Perform follow-ups and ensure the accuracy of eligibility-related information.

  • Oversee clinical trial activities and work closely with clinical research personnel.

  • Conduct all medical examinations as outlined in the study protocol.

  • Evaluate adverse events, make appropriate medical decisions, and ensure proper follow-up to determine resolution.

  • Interact with clients during on-site visits to address safety concerns.

  • Participate in on-call duties as required.

  • Perform additional clinical tasks as needed.

  • Ensure all activities comply with corporate policies, standard operating procedures (SOPs), and operational guidelines.

  • Carry out other assigned responsibilities as determined by management.

Note: This job description serves as a guide to the primary responsibilities and tasks associated with this role. It is not an exhaustive or permanent list of duties.


Qualifications

  • Ability to work effectively in a multidisciplinary clinical team.

  • Strong documentation skills with attention to detail.

  • Proficiency in computer applications, particularly Microsoft Word and Excel.

  • Excellent communication, presentation, and interpersonal skills, with the ability to inform, influence, and persuade effectively.

  • Certification in Advanced Cardiac Life Support (ACLS) or equivalent; must be certified or recertified to oversee study monitoring or have documented equivalent experience (internal training available).

  • Knowledge of ICH Good Clinical Practice (GCP) guidelines and other regulatory requirements.

  • Experience in a customer service-driven environment.

  • Strong understanding of the pharmaceutical industry and Contract Research Organizations (CROs), with an in-depth knowledge of clinical operations.

Position Requirements for Canada:

  • English Proficiency: Ability to communicate fluently on specialized and technical topics, with strong written skills for preparing complex technical reports.

  • Active Membership: Must be an active member of the Collège des Médecins du Québec (CMQ).