Associate Medical Director – Oncologist

This is a fully remote position, open to applicants in Canada.

📋 Description

• Take full responsibility for maintaining the integrity and quality of the medical, clinical, and safety components of trials conducted by Allucent.

• Act as the medical monitor liaison for investigators and study site teams regarding protocol-related and participant safety inquiries.

• Offer medical monitoring assistance for assigned clinical studies by addressing medical queries, aiding in protocol interpretation, and reviewing clinical data.

• Support the project manager in discussions with clients concerning safety issues or concerns.

• Develop medical monitoring plans and other pertinent plans before study initiation.

• Evaluate serious adverse events (SAEs), SUSARs, and safety reports, while analyzing similar occurrences.

• Collaborate with the clinical data management team on MedDRA and WHO coding.

• Examine clinical study documents, such as protocols, informed consent forms, clinical study reports, and safety reports.

• Contribute to the establishment and execution of data safety monitoring boards and dose-escalation meetings.

• Engage in study start-up meetings, investigator meetings, and other relevant gatherings, delivering presentations as necessary.

• Provide immediate medical support on a 24/7 basis.

• Educate project teams on the medical aspects of trials and offer therapeutic area training.

• Review protocol deviations.

• Identify study-related risks and assist in developing risk management plans.

• Assess medical deliverables, help with budget tracking, and attend therapeutic and drug development conferences.

• Maintain client relationships and take part in client assessments, visits, and proposal presentations.

⛳️ Requirements

• Medical degree (MD) required.

• Experience as an oncologist is essential.

• A minimum of three years of relevant professional experience with substantial expertise in oncology.

• Strong understanding of GxP standards.

• Must be in good standing with local, provincial, and national regulatory and licensing authorities, as well as certification bodies.

• Familiarity with applicable regulatory requirements, including GDPR/HIPAA, CFR/CTR/CTD.

• Exceptional written and verbal communication skills.

• Proficient in English.

• Capacity to thrive in the dynamic environment of a growing company.

• Excellent administrative skills.

• Proficient in Microsoft Word, Excel, and PowerPoint.

🏝️ Benefits

• Comprehensive benefits package tailored to the workplace location.

• Competitive salary based on location.

• Departmental training and education budget dedicated to professional development.

• Flexible working hours (where feasible).

• Options for remote or hybrid work based on location.

• Opportunities for leadership roles and access to mentorship.

• Participation in our buddy program, available for both new hires and existing employees.

• Opportunities for internal mobility and career advancement.

• Employee referral program with financial rewards.

• Access to online training for both soft and technical skills through ADP and our internal platforms.

• Eligibility for our spot bonus program, which rewards outstanding project contributions.

• Eligibility for our loyalty rewards program, recognizing long-term service and commitment.