Associate Medical Director – Oncologist

Allucent

Associate Medical Director at Allucent ensuring medical integrity of oncology clinical trials. Offering remote work support in managing safety and quality for studies conducted in Brazil.

Posted 7/31/2026full-timeRemote • 🇧🇷 BrazilLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive Oncology expertise and medical monitoring capabilities, ensuring adherence to protocols and scientific validity of clinical data. Proficient in regulatory compliance and effective communication with clients and project teams.

Highest-signal resume keywords

MD DegreeOncology ExpertiseGxP KnowledgeRegulatory Compliance (GDPR/HIPAA, CFR/CTR/CTD)Strong Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Soft Skills

Client FocusedOutgoingAdministrative Excellence

Tools & Technologies

WordExcelPowerPoint

Industry Keywords

Medical Monitor SupportClinical StudiesSerious Adverse Events ReviewData Safety BoardsProtocol Deviations

About the role

Key responsibilities & impact

**In this role your key tasks will include:**
- Independently provide medical monitor support to assigned clinical studies, for example answering medical questions from study team and/or site, assist with protocol interpretation and medical review of generated data including but not limited to clinical laboratory data and case report forms as necessary to ensure adherence to the protocol, consistency and scientific validity of the data. When appropriate, and with the necessary support from senior colleagues, assist the Project Manager in discussions with clients on safety issues or concerns that may have arisen
- Prepare the Medical Monitoring and other relevant plans for assigned studies conducted by Allucent prior to the start of the study and in accordance to deliverables contracted.
- Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events
- Assist clinical data management with MedDRA and WHO coding in assigned trials
- Assist by reviewing clinical study documents for medical consistency and relevance, with support of senior medical team members if needed, including but not limited to the clinical trial protocol (CTP), the Informed Consent (ICF) and clinical study report (CSR) other safety reports (e.g., DSUR, PSUR)
- Assist in the set up and conduct of Data Safety Boards (DSMB, DMB or similar) and Dose escalation meetings (DEC)
- Attend, participate and present in Kick-Off, Investigators’ meeting, and other relevant meetings in assigned projects, as requested.
- Provide 24/7 urgent medical support for medical and safety advice if required
- Training of project teams on medical aspects of the trial and therapeutic training as required
- Review of Protocol Deviations
- Identify study risks and provide input to the Risk plan
- Review and understand study medical deliverables laid down in the assigned study’s contract with support of senior colleagues and help track budget spent throughout their assigned study(ies)
- Attends and may need to present at major therapeutic conferences and drug development conferences
- Assure good communication and relationships with (future) clients
- Contribute and take part with support from senior colleagues as needed in client evaluations, visits and bid defenses

Requirements

What you’ll need

**To be successful you will possess:**
- MD degree
- Experience as Oncologist
- Minimum 3 years of relevant work experience with solid Oncology expertise
- Good knowledge of GxP
- Good standing with local, state (in the US), and national licensing and regulatory authorities and certifying bodies
- GDPR/HIPAA, CFR/CTR/CTD and applicable (local) regulatory requirements understanding
- Strong written and verbal communication skills including good command of English language
- Representative, outgoing and client focused
- Ability to work in a fast-paced challenging environment of a growing company
- Administrative excellence
- Proficiency with various computer applications such as Word, Excel, and PowerPoint required

Benefits

Comp & perks

**Benefits of working at Allucent include:**
- Comprehensive benefits package per location
- Competitive salaries per location
- Departmental Study/Training Budget for furthering professional development
- Flexible Working hours (within reason)
- Opportunity for remote/hybrid* working depending on location
- Leadership and mentoring opportunities
- Participation in our Buddy Program as a new or existing employee
- Internal growth opportunities and career progression
- Financially rewarding internal employee referral program
- Access to online soft-skills and technical training via ADP and internal platforms
- Eligibility for our Spot Bonus Award Program in recognition of going above and beyond on projects
- Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees