Allucent

Global drug development services for biotech

Associate Medical Director / Medical Director Oncologist

Biology & BiotechConfirmed live in the last 24 hours

Full-timeSão Paulo, State of São Paulo, BrazilRemote

About the Job

Requirements

An MD degree is required.
Experience as an oncologist is required, with at least 3 years of relevant work experience and solid oncology expertise.
Good knowledge of GxP is required.
Good standing with local, state (in the US), and national licensing and regulatory authorities and certifying bodies is required.
Understanding of GDPR/HIPAA, CFR/CTR/CTD, and applicable local regulatory requirements is required.
A good command of English, including strong written and verbal communication, is required.
The candidate must be representative, outgoing, and client-focused.
The candidate must be able to work in a fast-paced, challenging environment at a growing company.
Administrative excellence is required.
Proficiency with Word, Excel, PowerPoint, and various computer applications is required.

Responsibilities

Independently provide medical-monitor support for assigned clinical studies, answer medical questions from study teams or sites, assist with protocol interpretation and medical review of generated data (including clinical laboratory data and case report forms), and ensure protocol adherence, data consistency, and scientific validity.
When appropriate and with support from senior colleagues, assist the Project Manager in client discussions about safety issues or concerns.
Prepare medical-monitoring and other relevant plans for assigned studies before study start, in accordance with contracted deliverables.
Review Serious Adverse Events, SUSARs, and safety narratives, and perform Analysis of Similar Events.
Assist clinical data management with MedDRA and WHO coding in assigned trials.
Review clinical study documents for medical consistency and relevance, with support from senior medical team members when needed, including clinical trial protocols, informed consent forms, clinical study reports, and other safety reports such as DSURs and PSURs.
Assist with setting up and conducting Data Safety Boards and dose-escalation meetings.
Attend, participate in, and present at kick-off, investigators’ meetings, and other relevant project meetings as requested.
Provide urgent medical and safety advice 24/7 when required.
Train project teams on medical aspects of trials and provide therapeutic training as required.
Review protocol deviations.
Identify study risks and provide input to the risk plan.
Review and understand assigned studies’ medical deliverables in their contracts, with senior-colleague support, and help track study budgets.
Attend and, when needed, present at major therapeutic and drug-development conferences.
Maintain good communication and relationships with current and prospective clients.
Contribute, with support from senior colleagues as needed, to client evaluations, visits, and bid defenses.

Associate Medical Director / Medical Director Oncologist (Brazil)

Allucent · São Paulo, Brazil (Remote) · Full-time · Posted 2026-07-31

Workplace: remote

Department: Medical Affairs

Description

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for an Associate Medical Director/Medical Director to join our A-team (remote). As an Associate Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent, serving as the medical monitor contact in study protocols to investigators and study sites team regarding protocol related questions and safety of the subjects enrolled. Experience in Oncology is a requirement for this position.

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

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

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

Disclaimers:

*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.

“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”

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About the Company

Allucent

Global drug development services for biotech

Allucent provides global drug development services aimed at small and mid-sized biotech firms. Its offerings include therapeutic strategies, clinical trial operations, biometrics, and clinical pharmacology to support regulatory planning and execution. The company works by partnering with biotech teams to design and run clinical studies, extend in-house capabilities, and ensure accurate data collection and analysis across more than 60 countries. It differentiates itself by focusing on smaller biotech clients with end-to-end, globally coordinated development programs, backed by deep regulatory and scientific expertise and long-term collaborations. The goal is to help clients bring new therapies to market safely and efficiently through practical, hands-on development support.

Company size: 1,001-5,000
Company stage: Not listed
Total funding: Not listed
Headquarters: Cary, NC
Founded: 2022

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