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Clinical Research Medical Monitor Jobs (NOW HIRING)

ICON Clinical Research

Medical Monitor

Lenexa, KS · On-site

As a Medical Director, Clinical Research & Development at ICON, you will provide medical leadership and strategic direction to clinical development programs. We are looking for a board certified ...

ICON

Medical Monitor

Medical Monitor ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

410 ICR United States USA

Medical Monitor

United, PA · On-site

Medical Monitor ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Massgeneralbrigham

Clinical Research Monitor

Boston, MA

$50K - $82K/yr

We believe that high-performing teams drive groundbreaking medical discoveries and invite all ... At least 1-2 years of clinical research experience required * Previous experience with monitoring ...

Taiho Oncology

... medical monitor for various clinical phase 1 - 3 trials, and assisting the Clinical Research ... Scientist Manager to contribute to CRS process improvement, as needed. Performance Objectives: Uses ...

Praxis Precision Medicines, Inc.

Clinical Medical Monitor

$18.50 - $23.50/hr

Clinical trial experience with responsibility for medical monitoring, clinical safety, or related medical oversight. The position may be hired at the Director or Senior Director level based on the ...

Confluence Health

ARNP - RESEARCH

Wenatchee, WA · On-site

$65.87 - $79.81/hr

... Clinical Research Medical Director and provides direction and oversight to peers during their ... monitoring of potential adverse events, assigning and dispensing research medications ...

Praxis Precision Medicines, Inc.

Clinical Medical Monitor

OR · On-site +1

$18 - $23/hr

Clinical trial experience with responsibility for medical monitoring, clinical safety, or related medical oversight. The position may be hired at the Director or Senior Director level based on the ...

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Senior Director, Clinical Research-Medical Director (Oncology)

San Francisco, CA • On-site

Vir Biotechnology
Biotechnology Research and Development • 51 - 200 employees
Learn more about Vir Biotechnologyexternal

$235K - $329K/yr

Full-time

Medical, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN® dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.
Vir Biotechnology has exclusive rights to the universal PRO-XTEN® masking platform for oncology and infectious disease. PRO-XTEN® is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.
We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.
THE OPPORTUNITY
The Senior Director, Clinical Research (Oncology) will serve as a Medical Director/Medical Monitor within Oncology Clinical Development, providing medical leadership for ongoing clinical trials and ensuring the safety of patients enrolled across Vir Bio's oncology studies.
This role will be responsible for medical monitoring activities, clinical decision making, safety oversight, protocol execution, investigator engagement, and cross-functional collaboration throughout the lifecycle of clinical trials. The successful candidate will be an experienced Oncology MD with deep expertise in clinical research, medical monitoring, and oncology drug development across early and late-stage studies.
The role requires a physician leader with a strong track record of serving as a Medical Monitor and Clinical Research Physician, partnering closely with Clinical Operations, Clinical Scientists, Pharmacovigilance, Biometrics, and Regulatory teams to ensure safe, high-quality study execution.
This role is located in our San Francisco headquarters with an expectation of at least 3 days per week in office.
WHAT YOU'LL DO
  • Serve as the lead Medical Monitor and Clinical Research Physician for one or more oncology clinical trials, providing ongoing medical oversight and patient-level clinical decision-making
  • Review and interpret emerging safety and efficacy data, assess adverse events and safety signals, and partner with Pharmacovigilance to support benefit-risk assessments and patient safety
  • Act as the primary medical contact for investigators and study sites, providing guidance on patient eligibility, safety management, protocol implementation, and complex clinical questions
  • Lead medical monitoring activities across Phase 1-3 studies, ensuring high-quality study conduct, data integrity, protocol compliance, and regulatory readiness
  • Contribute to the development of study protocols, amendments, informed consent forms, safety management plans, clinical study reports, and clinical sections of regulatory submissions
  • Partner closely with Clinical Operations, Clinical Scientists, Biometrics, Regulatory, Translational Medicine, and Safety to support study execution, data review, and key development decisions
  • Present clinical findings, safety updates, and study recommendations to internal governance committees, executive leadership, and external stakeholders, including regulatory agencies as needed
  • Participate in investigator meetings, safety review committees, advisory boards, and regulatory interactions, serving as a medical expert and representative for assigned programs
  • Mentor junior team members and contribute to the continued growth of medical monitoring and clinical development capabilities across the organization

WHO YOU ARE AND WHAT YOU BRING
  • MD required; board certification in Oncology, Hematology/Oncology, or a related specialty strongly preferred
  • 12+ years of clinical research and drug development experience within biotechnology, pharmaceutical, academic, or CRO environments
  • Deep experience serving as a Medical Monitor and Clinical Research Physician within oncology drug development
  • Strong experience managing patient safety oversight and medical monitoring activities across oncology clinical trials
  • Demonstrated expertise supporting Phase 1, Phase 2, and Phase 3 oncology studies
  • Experience reviewing and interpreting patient-level safety and efficacy data
  • Strong understanding of oncology clinical trial design, GCP/ICH guidelines, regulatory requirements, and safety reporting obligations
  • Experience collaborating with Pharmacovigilance teams on safety signal detection, safety review committees, and benefit-risk assessments
  • Experience supporting regulatory submissions and health authority interactions preferred.
  • Excellent communication skills and ability to engage investigators, key opinion leaders, and cross-functional teams

#LI-AS1
#LI-Onsite
WHO WE ARE AND WHAT WE OFFER
The expected salary range for this position is $235,500 to $329,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.
Vir Biotechnology's compensation and benefits are aligned with the current market and commensurate with the person's experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.
Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.
This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.
Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.
For hires based in the United States, Vir Biotechnology, participates in E-Verify.
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