About the Company
Global BioSolutions Inc. is a leading Contract Research Organization (CRO) dedicated to accelerating drug development and improving global health. With a presence across continents, we partner with pharmaceutical, biotechnology, and medical device companies to deliver high-quality clinical research services. Our commitment to innovation, integrity, and patient safety drives our mission, and we are proud to offer a dynamic work environment where professionals can thrive and make a tangible impact. We embrace diversity and foster a collaborative culture that encourages growth and continuous learning.
Job Description
We are seeking a dedicated and experienced Clinical Research Associate (CRA) to join our growing team in Wallaceburg, Ontario. This exciting opportunity comes with a comprehensive global relocation package, underscoring our commitment to attracting top talent worldwide. As a CRA, you will be instrumental in the successful execution of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements. You will monitor various phases of clinical studies, manage site relationships, and contribute significantly to the integrity and quality of our research data. This role requires a keen eye for detail, strong communication skills, and a passion for advancing medical science. Join Global BioSolutions Inc. and be part of a team that is making a difference in patients’ lives globally.
Key Responsibilities
- Conduct comprehensive site monitoring visits (pre-study, initiation, routine, and close-out) to ensure compliance with study protocols, GCP, and regulatory guidelines.
- Verify the accuracy and completeness of case report forms (CRFs) against source documents and ensure timely resolution of data queries.
- Manage and maintain essential trial documents, ensuring they are audit-ready at all times.
- Provide ongoing training and support to investigative site staff on study procedures, regulatory requirements, and data collection.
- Collaborate effectively with cross-functional teams, including project managers, data managers, and regulatory affairs.
- Participate in investigator meetings and prepare detailed monitoring reports.
- Identify and escalate potential issues or risks related to study conduct to the project team.
- Ensure the safety and well-being of study participants are prioritized throughout the trial.
Required Skills
- Minimum of 2 years of experience as a Clinical Research Associate or equivalent in a CRO or pharmaceutical setting.
- Bachelor's degree in a life science, nursing, or related health field.
- Thorough understanding of ICH-GCP guidelines and applicable regulatory requirements.
- Excellent written and verbal communication skills in English.
- Strong organizational skills and attention to detail.
- Ability to work independently and manage multiple priorities effectively.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Valid driver's license and ability to travel as required.
Preferred Qualifications
- Master's degree or higher in a relevant scientific discipline.
- Clinical research certification (e.g., ACRP, SoCRA).
- Experience across various therapeutic areas, particularly oncology, cardiology, or rare diseases.
- Familiarity with electronic data capture (EDC) systems.
- Proficiency in additional languages.
Perks & Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive global relocation package, including visa support, travel assistance, and temporary housing.
- Generous health, dental, and vision insurance plans.
- Retirement savings plan with company matching contributions.
- Paid time off and holidays.
- Opportunities for professional development and continuous learning.
- Career advancement pathways within a global organization.
- Employee wellness programs and mental health support.
- Collaborative and inclusive work environment.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
⚠️ Important Disclaimer
Welcome to Courierser Jobs. We publish job opportunities aggregated from public sources, employers, and job portals. We never charge any fees to access or use our website; all information is provided entirely for free.
Courierser Jobs does not directly offer or manage these positions, nor are we directly involved in the hiring process for the vacancies published on https://job.courierser.com.
If you suspect a fraudulent listing or have any questions, please contact us at techturna@gmail.com.