MEDICAL MONITOR / SENIOR MEDICAL MONITOR
- Hiring from
- Australia
- Work type
- Remote
- Posted
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Medical Monitor / Senior Medical Monitor
Location: Remote - Australia,
Category: Clinical Development and Operations
Salary: Apply for details
Country: Australia
Employment: Direct Hire/Perm
Worksite: Remote
Apply For This Position
Job Description
Senior Medical Monitor
Australia | Remote
The Opportunity
Our client is a growing clinical research organisation seeking an experienced physician to provide medical monitoring and safety oversight across a portfolio of clinical studies.
Working closely with investigators, sponsors, and cross-functional study teams, you will provide medical leadership throughout the lifecycle of clinical trials, ensuring participant safety, protocol compliance, and high-quality study delivery. This is an excellent opportunity for a medically qualified professional who enjoys operating in a collaborative, fast-paced clinical development environment.
Key Responsibilities
Location: Remote - Australia,
Category: Clinical Development and Operations
Salary: Apply for details
Country: Australia
Employment: Direct Hire/Perm
Worksite: Remote
Apply For This Position
Job Description
Senior Medical Monitor
Australia | Remote
The Opportunity
Our client is a growing clinical research organisation seeking an experienced physician to provide medical monitoring and safety oversight across a portfolio of clinical studies.
Working closely with investigators, sponsors, and cross-functional study teams, you will provide medical leadership throughout the lifecycle of clinical trials, ensuring participant safety, protocol compliance, and high-quality study delivery. This is an excellent opportunity for a medically qualified professional who enjoys operating in a collaborative, fast-paced clinical development environment.
Key Responsibilities
- Provide medical and safety oversight for assigned clinical trials.
- Review and contribute to study documentation, including protocols, amendments, investigator brochures, informed consent forms, and clinical study reports.
- Support investigators and study teams with participant eligibility assessments and protocol-related medical queries.
- Review clinical data, medical coding outputs, safety data, and protocol deviations.
- Provide therapeutic area and protocol training to internal teams and investigator sites.
- Participate in investigator meetings, study kick-offs, data review meetings, and sponsor discussions.
- Contribute to medical monitoring plans and ongoing medical monitoring activities throughout study conduct.
- Support regulatory and ethics committee responses where medical expertise is required.
- Provide input into proposals, bid defences, and client-facing activities as required.
Experience & Qualifications
We are interested in physicians who combine strong clinical judgement with an understanding of clinical development and patient safety. Candidates should be comfortable operating in a matrix environment, collaborating across clinical operations, pharmacovigilance, project management, data management, biostatistics, and sponsor stakeholder groups.
Location
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us(opens in new tab) directly so that we can explore the appropriate arrangements.
Fraud Alert
Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
- Medical degree from a recognised institution.
- Approximately 8+ years of relevant medical experience.
- Experience supporting clinical trials within a CRO, biotechnology, pharmaceutical, or clinical research environment.
- Strong understanding of ICH-GCP and clinical trial conduct.
- Experience reviewing safety data, protocols, informed consent documents, and clinical study reports.
- Ability to work effectively with investigators, sponsors, and multidisciplinary study teams.
- Strong written and verbal communication skills.
- Fluent English required. Additional languages would be advantageous.
We are interested in physicians who combine strong clinical judgement with an understanding of clinical development and patient safety. Candidates should be comfortable operating in a matrix environment, collaborating across clinical operations, pharmacovigilance, project management, data management, biostatistics, and sponsor stakeholder groups.
Location
- Australia-based role
- Remote working environment
- Melbourne or Sydney preferred
- Competitive salary and bonus package
- Flexible working environment
- Opportunity to work on a diverse portfolio of clinical studies
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us(opens in new tab) directly so that we can explore the appropriate arrangements.
Fraud Alert
Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it’s from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.
The Planet Group of Companies is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
