Job Description Summary
We are seeking a highly motivated and scientifically driven Clinical Research Medical Advisor (CRMA) to provide strategic and tactical leadership for country-level clinical development activities. The CRMA will play a pivotal role in the planning execution and oversight of clinical trials ensuring alignment with global development strategies and adherence to regulatory and ethical standards. This role involves close collaboration with cross-functional teams to optimize trial implementation enhance patient recruitment and uphold data integrity and patient safety.
Job Description
Key Responsibilities:
- Provide clinical strategic and tactical leadership for country clinical development and research programs or trials.
- Gather inform and act on clinical medical or scientific insights to optimize clinical trial implementation.
- Drive the identification and involvement of qualified investigators and overcome clinical recruitment hurdles.
- Ensure adherence to safety standards and clinical data quality in the country.
- Collaborate with country functions to ensure successful trial start-up timely recruitment and mitigation of potential delays.
- Provide clinical or medical expertise during interactions with external experts and regulatory authorities.
- Support planning implementation and follow-up of scientific clinical or medical components of regulatory inspections and internal audits.
Essential Requirements:
- Scientific degree (M.D. Ph.D.) with subspecialty training desirable.
- Minimum 2-5 years of clinical development experience in the pharmaceutical industry or clinical practice.
- Strong understanding of the overall clinical development process and ICH/GCP principles.
- Ability to manage studies from a scientific medical or clinical perspective and solve complex issues.
- Effective leadership and communication skills to motivate cross-functional teams.
- Willingness to travel as when needed.
Skills:
- Clinical Monitoring.
- Clinical Research.
- Clinical Trial Protocol.
- Clinical Trials.
- Decision Making Skills.
- Drug Development.
- Health Sciences.
- Lifesciences.
- Regulatory Compliance.
Languages :
Skills Desired
Clinical Monitoring Clinical Research Clinical Trial Protocol Clinical Trials Decision Making Skills Drug Development Health Sciences Lifesciences Regulatory Compliance
Required Experience:
Unclear Seniority
Job Description SummaryWe are seeking a highly motivated and scientifically driven Clinical Research Medical Advisor (CRMA) to provide strategic and tactical leadership for country-level clinical development activities. The CRMA will play a pivotal role in the planning execution and oversight of cli...
Job Description Summary
We are seeking a highly motivated and scientifically driven Clinical Research Medical Advisor (CRMA) to provide strategic and tactical leadership for country-level clinical development activities. The CRMA will play a pivotal role in the planning execution and oversight of clinical trials ensuring alignment with global development strategies and adherence to regulatory and ethical standards. This role involves close collaboration with cross-functional teams to optimize trial implementation enhance patient recruitment and uphold data integrity and patient safety.
Job Description
Key Responsibilities:
- Provide clinical strategic and tactical leadership for country clinical development and research programs or trials.
- Gather inform and act on clinical medical or scientific insights to optimize clinical trial implementation.
- Drive the identification and involvement of qualified investigators and overcome clinical recruitment hurdles.
- Ensure adherence to safety standards and clinical data quality in the country.
- Collaborate with country functions to ensure successful trial start-up timely recruitment and mitigation of potential delays.
- Provide clinical or medical expertise during interactions with external experts and regulatory authorities.
- Support planning implementation and follow-up of scientific clinical or medical components of regulatory inspections and internal audits.
Essential Requirements:
- Scientific degree (M.D. Ph.D.) with subspecialty training desirable.
- Minimum 2-5 years of clinical development experience in the pharmaceutical industry or clinical practice.
- Strong understanding of the overall clinical development process and ICH/GCP principles.
- Ability to manage studies from a scientific medical or clinical perspective and solve complex issues.
- Effective leadership and communication skills to motivate cross-functional teams.
- Willingness to travel as when needed.
Skills:
- Clinical Monitoring.
- Clinical Research.
- Clinical Trial Protocol.
- Clinical Trials.
- Decision Making Skills.
- Drug Development.
- Health Sciences.
- Lifesciences.
- Regulatory Compliance.
Languages :
Skills Desired
Clinical Monitoring Clinical Research Clinical Trial Protocol Clinical Trials Decision Making Skills Drug Development Health Sciences Lifesciences Regulatory Compliance
Required Experience:
Unclear Seniority
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