Associate Medical Director – Oncologist

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

📋 Description

• **In this position, your primary responsibilities will encompass:**

• - Providing independent medical monitor support for assigned clinical studies, including addressing medical inquiries from the study team and/or site, assisting with protocol interpretation, and conducting medical reviews of generated data, such as clinical laboratory results and case report forms, to ensure protocol compliance, data consistency, and scientific validity. When appropriate, and with the necessary backing from senior colleagues, support the Project Manager in discussions with clients regarding any safety issues or concerns that may arise.

• - Developing the Medical Monitoring and other relevant plans for the studies conducted by Allucent prior to their commencement, in line with contractual deliverables.

• - Reviewing Serious Adverse Events, SUSARs, and safety narratives, along with performing analyses of similar events.

• - Assisting clinical data management with MedDRA and WHO coding for the assigned trials.

• - Reviewing clinical study documents for medical consistency and relevance, with support from senior medical team members as necessary, including but not limited to the clinical trial protocol (CTP), the Informed Consent (ICF), and clinical study report (CSR) as well as other safety reports (e.g., DSUR, PSUR).

• - Aiding in the establishment and conduct of Data Safety Boards (DSMB, DMB, or similar) and Dose Escalation Meetings (DEC).

• - Attending, participating in, and presenting at Kick-Off, Investigator meetings, and other relevant meetings for assigned projects, as requested.

• - Providing 24/7 urgent medical support for medical and safety advice as needed.

• - Training project teams on the medical aspects of the trial and providing therapeutic training as required.

• - Reviewing Protocol Deviations.

• - Identifying study risks and contributing input to the Risk plan.

• - Reviewing and understanding study medical deliverables outlined in the assigned study’s contract with support from senior colleagues and helping track budget expenditures throughout their assigned study(ies).

• - Attending and potentially presenting at major therapeutic conferences and drug development conferences.

• - Ensuring effective communication and relationships with (future) clients.

• - Contributing to and participating in client evaluations, visits, and bid defenses with support from senior colleagues as needed.

⛳️ Requirements

• **To thrive in this role, you will need to have:**

• - An MD degree.

• - Experience as an Oncologist.

• - A minimum of 3 years of relevant work experience with solid Oncology expertise.

• - A strong understanding of GxP.

• - Good standing with local, state (in the US), and national licensing and regulatory authorities, as well as certifying bodies.

• - An understanding of GDPR/HIPAA, CFR/CTR/CTD, and applicable (local) regulatory requirements.

• - Excellent written and verbal communication skills, including a strong command of the English language.

• - A representative, outgoing, and client-focused demeanor.

• - The ability to thrive in a fast-paced and challenging environment within a growing company.

• - Administrative excellence.

• - Proficiency in various computer applications, including Word, Excel, and PowerPoint.

🏝️ Benefits

• **Working at Allucent offers the following benefits:**

• - A comprehensive benefits package tailored to each location.

• - Competitive salaries based on location.

• - A departmental Study/Training Budget to enhance professional development.

• - Flexible working hours (within reason).

• - Opportunities for remote/hybrid working, depending on location.

• - Leadership and mentoring opportunities.

• - Participation in our Buddy Program for new or existing employees.

• - Internal growth opportunities and career progression.

• - A financially rewarding internal employee referral program.

• - Access to online soft-skills and technical training through ADP and internal platforms.

• - Eligibility for our Spot Bonus Award Program, recognizing outstanding contributions to projects.

• - Eligibility for our Loyalty Award Program, honoring long-term employee commitment and loyalty.