215 Medical Instruction jobs in India
Mbbs Doctor(Training Clinical Pharmacist)
Bengaluru, Karnataka
Vedita Ventures
Posted today
Job Viewed
Job Description
**Position/ Title**
Patient Lead - Care Team
**Reports to**
Director
**No. of Reportees**
2
**Purpose of this position**
Establish and sustain a strong clinical foundation and continuous improvement of quality of life for the patients through strong clinical support and relevant patient engagement
Ensure high level of patient engagement and high awareness resulting in referring to their doctors at the right time
**Key Accountabilities/ Responsibilities**
High clinical quality in the Company’s programs and improvement in outcomes
of patients enrolled with the organisation
**Day to Day responsibilities**
Execute ongoing oversight on patient reviews by Clinical Pharmacists to ensure high quality clinical support and patient engagement.
Clinical review of patient engagements done by the Clinical Pharmacists
Training of Clinical Pharmacists on clinical matters and patient engagement which involves patients counseling and reviews, lifestyle and diet recommendations.
Working with Senior management to establish quality standards for patient reviews by Clinical Pharmacist. Update on the same on regular basis
At need, on line consult for the patients wrt their prescriptions, medication, lab reports etc.
Review of status of patient records for quality of information and remaining up to date on regulatory matters
Requires time flexibility as necessary to meet customer schedules and coordinate accordingly
**Competencies /**
**Skills Required**:
- Strong clinical assessment and diagnosis especially in the area of chronic conditions
- Detail oriented, even when faced with highly repetitive tasks.
- Must be able to work both with internal and external customers
- Comfortable in new environments and challenging healthcare conditions
- Must be able to work and interact with different group of people
- Regular professional updation
- Good leadership, communication and influencing skills
**Educational Qualifications**
**Minimum**:
MBBS and registration with State Medical Council
**Work Experience (Relevant**
**and Total Experience**
Ideally working in a practice or establishment that has high flow of patients with chronic illnesses with around 1 year experience
**Salary**: ₹50,000.00 - ₹75,000.00 per month
Schedule:
- Day shift
Application Question(s):
- Are you ready to train Clinical Pharmacist?
**Experience**:
- Practicing doctor(MBBS Qualified): 1 year (required)
Work Location: In person
Patient Lead - Care Team
**Reports to**
Director
**No. of Reportees**
2
**Purpose of this position**
Establish and sustain a strong clinical foundation and continuous improvement of quality of life for the patients through strong clinical support and relevant patient engagement
Ensure high level of patient engagement and high awareness resulting in referring to their doctors at the right time
**Key Accountabilities/ Responsibilities**
High clinical quality in the Company’s programs and improvement in outcomes
of patients enrolled with the organisation
**Day to Day responsibilities**
Execute ongoing oversight on patient reviews by Clinical Pharmacists to ensure high quality clinical support and patient engagement.
Clinical review of patient engagements done by the Clinical Pharmacists
Training of Clinical Pharmacists on clinical matters and patient engagement which involves patients counseling and reviews, lifestyle and diet recommendations.
Working with Senior management to establish quality standards for patient reviews by Clinical Pharmacist. Update on the same on regular basis
At need, on line consult for the patients wrt their prescriptions, medication, lab reports etc.
Review of status of patient records for quality of information and remaining up to date on regulatory matters
Requires time flexibility as necessary to meet customer schedules and coordinate accordingly
**Competencies /**
**Skills Required**:
- Strong clinical assessment and diagnosis especially in the area of chronic conditions
- Detail oriented, even when faced with highly repetitive tasks.
- Must be able to work both with internal and external customers
- Comfortable in new environments and challenging healthcare conditions
- Must be able to work and interact with different group of people
- Regular professional updation
- Good leadership, communication and influencing skills
**Educational Qualifications**
**Minimum**:
MBBS and registration with State Medical Council
**Work Experience (Relevant**
**and Total Experience**
Ideally working in a practice or establishment that has high flow of patients with chronic illnesses with around 1 year experience
**Salary**: ₹50,000.00 - ₹75,000.00 per month
Schedule:
- Day shift
Application Question(s):
- Are you ready to train Clinical Pharmacist?
**Experience**:
- Practicing doctor(MBBS Qualified): 1 year (required)
Work Location: In person
This advertiser has chosen not to accept applicants from your region.
0
Sr. Manager - QC & Training (Clinical Research)
Sun Pharmaceuticals, Inc
Posted 9 days ago
Job Viewed
Job Description
**YOUR TASKS AND RESPONSIBILITIES:**
This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable for Quality Compliance (QC) activities of Clinical Trial Medical Science team and Operations team, Clinical Trial Supply Management (CTSM) team, and Clinical Data Management team by way of Review of all study related activities, processes, procedures and adherence to applicable regulations and guidelines to ensure 24x7 Inspection/audit readiness.
This role will be responsible for establishing the procedures and trainings of teams which ensure protection of human subjects from research risk, reliability/Integrity of the data, and thereby assures internal consistency and Quality Compliance measures.
**Systems and Processes:**
+ Develop, implement and maintain a Quality Management System (QMS) for clinical trial team in consultation with Head Quality Compliance & Training and ensure oversight on team on quality aspect as per defined SOPs and applicable regulations.
+ Implement and oversee the Quality Compliance procedures/processes/systems for clinical trials managed by the Medical science and Clinical Operations department.
+ To assist in designing a process to write, review and approve the risk assessments for new trials and for ongoing projects and working closely with Project Managers and Operation Head as needed.
+ To ensure a process in place to provide assurance on review of all study documentation for accuracy, consistency and completeness.
+ Ensure effective systems and processes in place to maintain consistency and quality compliance parameters in medical science, operations, data management and drug depot for end-to-end activities of each function as per applicable regulatory requirements.
+ Work with Clinical Research QC team, Medical Science team, Clinical Operations team, Clinical Data Management team and Study Management team to create and implement study specific QC plans that outline the scope of Quality Compliance procedures to be followed during clinical trials, ensuring QC processes are in alignment with SOPs and study protocols.
+ Ensure completeness of training of study team on SOPs and job specific training as per role and responsibilities. Ensure periodic review of training files for all study team.
+ Assess and identify the training requirement of study team and ensure completion of training.
+ Well versed with electronic systems used in Clinical Trial operations, Data Management and Project Management which includes project specific deliverables tracking and important milestone related alarms, protocol compliance tracking, deviations tracking and electronic systems used for managing Trial Master File (TMF) and Drug accountability.
+ Assist in developing system/process to work with the clinical trial team to schedule pre-execution and post-execution QC activities to ensure that all requirements of the QC plans are planned as required and executed.
+ Plan, design, and update process and systems for clinical trial activities like development and utilization of QC assessment parameters and other QC tools designed to document/track the QC review process for clinical research activities in line with recent regulatory requirement.
+ Ensure Quality Management System at Medical Science, Data Management team, Operation team to ensure the department is ready for audit/inspection 24x7.
+ Ensure periodic review of Vendors and renewals as per applicable policies & procedures.
+ Identify and recommend process improvement initiatives where required.
+ Create and evaluate metrics to assess performance and implement plans for course correction.
**Activities:**
+ Should be effective team player who can work closely with different study teams and collaborate well with team members to achieve defined QC targets.
+ Develop and implement a risk-based and flexible approach to Quality Compliance (QC) within the function, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practices.
+ Identify and decide team members job specific SOP training requirements in view of their role and maintain oversight of training to ensure all team members are trained on each SOP as required.
+ Preparation of SOPs related to QC function and support in review of SOPs specific to Medical science, Clinical team and Data Management team.
+ Quality review of the clinical trial medical science related activities like Synopsis, Protocol, Clinical Study Report (CSR) and appendices, and SOPs in line with ICH GCP requirement, Indian and global regulatory requirement.
+ Quality review of the clinical trial operation related activities, related tools, plans and documentation like site feasibility, site selection visit, site initiation, Ethic committee documentation, monitoring site specific reports, Site Documents, logs and close out activities in line with ICH GCP requirement, Indian and global regulatory requirement.
+ Ensure Quality review of SOPs and oversight on quality parameters specific to Clinical Trial Supply Management (CTSM) and other activities like receipt, handling of study sample, labelling, storage, temperature monitoring systems and distribution to trial sites.
+ Final QC review of study close out activities including returned goods reconciliation, inventory destruction processing and archiving of documents.
+ Review and communication of QC findings to respective department in stipulated timelines.
+ Arrange monthly meeting or meetings as and when required depending on criticality of the issues with concerned team to discuss and communicate the findings from QC reviews to the internal stakeholders via QC summaries, reports as required.
+ Maintain the repository of QC findings as per the department and specific function and present the trend analysis, training requirement and action plan with timelines to Head Medical Affairs and clinical for course correction on quarterly basis.
+ Ensure training of SOPs, on job training and reviewing training files on regular basis.
+ QC review and Support in preparation of clinical study manuals/documents/Plan such as the IMP handling manual, Study plans.
+ Ensure record maintenance for all activities for traceability in line with regulatory requirement.
**WHO YOU ARE:**
+ >5 years experience in a CRO/Pharma/Biotech organization in Quality department with experience of Quality activities in Clinical Research department.
+ Strong eye for detail and ability to spot inconsistencies a must and good conflict management skills.
+ Must have experience in handling audits & inspections of DCGI, US FDA.
+ Thorough knowledge of recent GCP guidelines, ICMR guidelines, Drugs and Cosmetic Act regulations and other applicable regulations pertaining to clinical trials.
+ Experience of working in matrix business environments preferred.
+ Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.
+ Quality oriented mindset and skill set.
+ Experience in auditing processes and procedures, including the development of plans for corrective and preventive action (CAPA).
+ In-depth working knowledge of clinical trial regulations, good clinical practice (GCP) guidelines and other frameworks, and their implications for clinical research.
+ Proactive approach to reviewing, updating and improving processes based on current knowledge of the regulatory requirements.
+ Have strong analytical and problem-solving skills and the ability to present solutions.
+ Able to work under pressure and prioritize workload effectively, able to ensure timely completion of tasks to high quality in a matrix organization.
+ Eye for details, Sense of urgency & desire to excel.
+ Proficiency with Excel or other quality management systems/ tools.
+ Result oriented and performance driven.
+ Excellent interpersonal & communication skills to effectively interact with a broad range of audience.
**Job** location: Sun House, Goregaon East, Mumbai
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable for Quality Compliance (QC) activities of Clinical Trial Medical Science team and Operations team, Clinical Trial Supply Management (CTSM) team, and Clinical Data Management team by way of Review of all study related activities, processes, procedures and adherence to applicable regulations and guidelines to ensure 24x7 Inspection/audit readiness.
This role will be responsible for establishing the procedures and trainings of teams which ensure protection of human subjects from research risk, reliability/Integrity of the data, and thereby assures internal consistency and Quality Compliance measures.
**Systems and Processes:**
+ Develop, implement and maintain a Quality Management System (QMS) for clinical trial team in consultation with Head Quality Compliance & Training and ensure oversight on team on quality aspect as per defined SOPs and applicable regulations.
+ Implement and oversee the Quality Compliance procedures/processes/systems for clinical trials managed by the Medical science and Clinical Operations department.
+ To assist in designing a process to write, review and approve the risk assessments for new trials and for ongoing projects and working closely with Project Managers and Operation Head as needed.
+ To ensure a process in place to provide assurance on review of all study documentation for accuracy, consistency and completeness.
+ Ensure effective systems and processes in place to maintain consistency and quality compliance parameters in medical science, operations, data management and drug depot for end-to-end activities of each function as per applicable regulatory requirements.
+ Work with Clinical Research QC team, Medical Science team, Clinical Operations team, Clinical Data Management team and Study Management team to create and implement study specific QC plans that outline the scope of Quality Compliance procedures to be followed during clinical trials, ensuring QC processes are in alignment with SOPs and study protocols.
+ Ensure completeness of training of study team on SOPs and job specific training as per role and responsibilities. Ensure periodic review of training files for all study team.
+ Assess and identify the training requirement of study team and ensure completion of training.
+ Well versed with electronic systems used in Clinical Trial operations, Data Management and Project Management which includes project specific deliverables tracking and important milestone related alarms, protocol compliance tracking, deviations tracking and electronic systems used for managing Trial Master File (TMF) and Drug accountability.
+ Assist in developing system/process to work with the clinical trial team to schedule pre-execution and post-execution QC activities to ensure that all requirements of the QC plans are planned as required and executed.
+ Plan, design, and update process and systems for clinical trial activities like development and utilization of QC assessment parameters and other QC tools designed to document/track the QC review process for clinical research activities in line with recent regulatory requirement.
+ Ensure Quality Management System at Medical Science, Data Management team, Operation team to ensure the department is ready for audit/inspection 24x7.
+ Ensure periodic review of Vendors and renewals as per applicable policies & procedures.
+ Identify and recommend process improvement initiatives where required.
+ Create and evaluate metrics to assess performance and implement plans for course correction.
**Activities:**
+ Should be effective team player who can work closely with different study teams and collaborate well with team members to achieve defined QC targets.
+ Develop and implement a risk-based and flexible approach to Quality Compliance (QC) within the function, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practices.
+ Identify and decide team members job specific SOP training requirements in view of their role and maintain oversight of training to ensure all team members are trained on each SOP as required.
+ Preparation of SOPs related to QC function and support in review of SOPs specific to Medical science, Clinical team and Data Management team.
+ Quality review of the clinical trial medical science related activities like Synopsis, Protocol, Clinical Study Report (CSR) and appendices, and SOPs in line with ICH GCP requirement, Indian and global regulatory requirement.
+ Quality review of the clinical trial operation related activities, related tools, plans and documentation like site feasibility, site selection visit, site initiation, Ethic committee documentation, monitoring site specific reports, Site Documents, logs and close out activities in line with ICH GCP requirement, Indian and global regulatory requirement.
+ Ensure Quality review of SOPs and oversight on quality parameters specific to Clinical Trial Supply Management (CTSM) and other activities like receipt, handling of study sample, labelling, storage, temperature monitoring systems and distribution to trial sites.
+ Final QC review of study close out activities including returned goods reconciliation, inventory destruction processing and archiving of documents.
+ Review and communication of QC findings to respective department in stipulated timelines.
+ Arrange monthly meeting or meetings as and when required depending on criticality of the issues with concerned team to discuss and communicate the findings from QC reviews to the internal stakeholders via QC summaries, reports as required.
+ Maintain the repository of QC findings as per the department and specific function and present the trend analysis, training requirement and action plan with timelines to Head Medical Affairs and clinical for course correction on quarterly basis.
+ Ensure training of SOPs, on job training and reviewing training files on regular basis.
+ QC review and Support in preparation of clinical study manuals/documents/Plan such as the IMP handling manual, Study plans.
+ Ensure record maintenance for all activities for traceability in line with regulatory requirement.
**WHO YOU ARE:**
+ >5 years experience in a CRO/Pharma/Biotech organization in Quality department with experience of Quality activities in Clinical Research department.
+ Strong eye for detail and ability to spot inconsistencies a must and good conflict management skills.
+ Must have experience in handling audits & inspections of DCGI, US FDA.
+ Thorough knowledge of recent GCP guidelines, ICMR guidelines, Drugs and Cosmetic Act regulations and other applicable regulations pertaining to clinical trials.
+ Experience of working in matrix business environments preferred.
+ Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.
+ Quality oriented mindset and skill set.
+ Experience in auditing processes and procedures, including the development of plans for corrective and preventive action (CAPA).
+ In-depth working knowledge of clinical trial regulations, good clinical practice (GCP) guidelines and other frameworks, and their implications for clinical research.
+ Proactive approach to reviewing, updating and improving processes based on current knowledge of the regulatory requirements.
+ Have strong analytical and problem-solving skills and the ability to present solutions.
+ Able to work under pressure and prioritize workload effectively, able to ensure timely completion of tasks to high quality in a matrix organization.
+ Eye for details, Sense of urgency & desire to excel.
+ Proficiency with Excel or other quality management systems/ tools.
+ Result oriented and performance driven.
+ Excellent interpersonal & communication skills to effectively interact with a broad range of audience.
**Job** location: Sun House, Goregaon East, Mumbai
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
This advertiser has chosen not to accept applicants from your region.
1
Sr. Manager - QC & Training (Clinical Research)
Mumbai, Maharashtra
SUN PHARMA
Posted today
Job Viewed
Job Description
YOUR TASKS AND RESPONSIBILITIES: This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable for Quality Compliance (QC) activities of Clinical Trial Medical Science team and Operations team, Clinical Trial Supply Management (CTSM) team, and Clinical Data Management team by way of Review of all study related activities, processes, procedures and adherence to applicable regulations and guidelines to ensure 24x7 Inspection/audit readiness. This role will be responsible for establishing the procedures and trainings of teams which ensure protection of human subjects from research risk, reliability/Integrity of the data, and thereby assures internal consistency and Quality Compliance measures. Systems and Processes: Develop, implement and maintain a Quality Management System (QMS) for clinical trial team in consultation with Head Quality Compliance & Training and ensure oversight on team on quality aspect as per defined SOPs and applicable regulations. Implement and oversee the Quality Compliance procedures/processes/systems for clinical trials managed by the Medical science and Clinical Operations department. To assist in designing a process to write, review and approve the risk assessments for new trials and for ongoing projects and working closely with Project Managers and Operation Head as needed. To ensure a process in place to provide assurance on review of all study documentation for accuracy, consistency and completeness. Ensure effective systems and processes in place to maintain consistency and quality compliance parameters in medical science, operations, data management and drug depot for end-to-end activities of each function as per applicable regulatory requirements. Work with Clinical Research QC team, Medical Science team, Clinical Operations team, Clinical Data Management team and Study Management team to create and implement study specific QC plans that outline the scope of Quality Compliance procedures to be followed during clinical trials, ensuring QC processes are in alignment with SOPs and study protocols. Ensure completeness of training of study team on SOPs and job specific training as per role and responsibilities. Ensure periodic review of training files for all study team. Assess and identify the training requirement of study team and ensure completion of training. Well versed with electronic systems used in Clinical Trial operations, Data Management and Project Management which includes project specific deliverables tracking and important milestone related alarms, protocol compliance tracking, deviations tracking and electronic systems used for managing Trial Master File (TMF) and Drug accountability. Assist in developing system/process to work with the clinical trial team to schedule pre-execution and post-execution QC activities to ensure that all requirements of the QC plans are planned as required and executed. Plan, design, and update process and systems for clinical trial activities like development and utilization of QC assessment parameters and other QC tools designed to document/track the QC review process for clinical research activities in line with recent regulatory requirement. Ensure Quality Management System at Medical Science, Data Management team, Operation team to ensure the department is ready for audit/inspection 24x7. Ensure periodic review of Vendors and renewals as per applicable policies & procedures. Identify and recommend process improvement initiatives where required. Create and evaluate metrics to assess performance and implement plans for course correction. Activities: Should be effective team player who can work closely with different study teams and collaborate well with team members to achieve defined QC targets. Develop and implement a risk-based and flexible approach to Quality Compliance (QC) within the function, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practices. Identify and decide team members job specific SOP training requirements in view of their role and maintain oversight of training to ensure all team members are trained on each SOP as required. Preparation of SOPs related to QC function and support in review of SOPs specific to Medical science, Clinical team and Data Management team. Quality review of the clinical trial medical science related activities like Synopsis, Protocol, Clinical Study Report (CSR) and appendices, and SOPs in line with ICH GCP requirement, Indian and global regulatory requirement. Quality review of the clinical trial operation related activities, related tools, plans and documentation like site feasibility, site selection visit, site initiation, Ethic committee documentation, monitoring site specific reports, Site Documents, logs and close out activities in line with ICH GCP requirement, Indian and global regulatory requirement. Ensure Quality review of SOPs and oversight on quality parameters specific to Clinical Trial Supply Management (CTSM) and other activities like receipt, handling of study sample, labelling, storage, temperature monitoring systems and distribution to trial sites. Final QC review of study close out activities including returned goods reconciliation, inventory destruction processing and archiving of documents. Review and communication of QC findings to respective department in stipulated timelines. Arrange monthly meeting or meetings as and when required depending on criticality of the issues with concerned team to discuss and communicate the findings from QC reviews to the internal stakeholders via QC summaries, reports as required. Maintain the repository of QC findings as per the department and specific function and present the trend analysis, training requirement and action plan with timelines to Head Medical Affairs and clinical for course correction on quarterly basis. Ensure training of SOPs, on job training and reviewing training files on regular basis. QC review and Support in preparation of clinical study manuals/documents/Plan such as the IMP handling manual, Study plans. Ensure record maintenance for all activities for traceability in line with regulatory requirement. WHO YOU ARE: >5 years experience in a CRO/Pharma/Biotech organization in Quality department with experience of Quality activities in Clinical Research department. Strong eye for detail and ability to spot inconsistencies a must and good conflict management skills. Must have experience in handling audits & inspections of DCGI, US FDA. Thorough knowledge of recent GCP guidelines, ICMR guidelines, Drugs and Cosmetic Act regulations and other applicable regulations pertaining to clinical trials. Experience of working in matrix business environments preferred. Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards. Quality oriented mindset and skill set. Experience in auditing processes and procedures, including the development of plans for corrective and preventive action (CAPA). In-depth working knowledge of clinical trial regulations, good clinical practice (GCP) guidelines and other frameworks, and their implications for clinical research. Proactive approach to reviewing, updating and improving processes based on current knowledge of the regulatory requirements. Have strong analytical and problem-solving skills and the ability to present solutions. Able to work under pressure and prioritize workload effectively, able to ensure timely completion of tasks to high quality in a matrix organization. Eye for details, Sense of urgency & desire to excel. Proficiency with Excel or other quality management systems/ tools. Result oriented and performance driven. Excellent interpersonal & communication skills to effectively interact with a broad range of audience.
Job location: Sun House, Goregaon East, Mumbai
This advertiser has chosen not to accept applicants from your region.
2
Medical Education Specialist
Bengaluru, Karnataka
Erba Mannheim
Posted today
Job Viewed
Job Description
Medical Education Specialist
Experience : 1-3 years of Experience in the Healthcare
Functional Area : Marketing
Qualification : MD Pathology
Work Location : Mumbai, Bangalore, Chennai, Delhi
Job Description :
This advertiser has chosen not to accept applicants from your region.
3
Medical Education Specialist
Chennai, Tamil Nadu
Erba Mannheim
Posted today
Job Viewed
Job Description
Medical Education Specialist
Experience : 1-3 years of Experience in the Healthcare
Functional Area : Marketing
Qualification : MD Pathology
Work Location : Mumbai, Bangalore, Chennai, Delhi
Job Description :
This advertiser has chosen not to accept applicants from your region.
4
Medical Education Specialist
Delhi, Delhi
Erba Mannheim
Posted today
Job Viewed
Job Description
Medical Education Specialist
Experience : 1-3 years of Experience in the Healthcare
Functional Area : Marketing
Qualification : MD Pathology
Work Location : Mumbai, Bangalore, Chennai, Delhi
Job Description :
This advertiser has chosen not to accept applicants from your region.
5
Medical Education Specialist
Mumbai, Maharashtra
Erba Mannheim
Posted today
Job Viewed
Job Description
Medical Education Specialist
Experience : 1-3 years of Experience in the Healthcare
Functional Area : Marketing
Qualification : MD Pathology
Work Location : Mumbai, Bangalore, Chennai, Delhi
Job Description :
This advertiser has chosen not to accept applicants from your region.
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6
Healthcare Specialist (AI Training)
Taskify
Posted 5 days ago
Job Viewed
Job Description
We're Hiring Healthcare Specialist For AI Training (Remote) | Earn Between $5,000 - $,000/Month
About the Role: Are you a medical professional with a passion for advancing AI? We are seeking medical experts to contribute to the training and refinement of cutting-edge artificial intelligence models. In this fully remote and flexible role, you will leverage your clinical knowledge to enhance AI's ability to perform diagnostic and reasoning tasks with precision and accuracy.
Who Can Join?
- Medical consultants
- Students MBBS / Nursing / BDS / BPT / Allied Health
- Health professionals, including doctors, nurses, physician assistants, and various allied health professionals like therapists, dietitians, and technicians, etc.
What You'll Do:
- Create and answer complex clinical questions to train AI in diagnostic and reasoning tasks.
- Review and analyse AI model responses for clinical soundness, scientific rigour, and relevance.
- Rank and assess AI outputs to identify strengths, weaknesses, and opportunities for improvement.
- Provide expert feedback to help improve the quality, accuracy, and logic of AI-generated content.
- You may be assigned to different projects based on your expertise and performance.
What We're Looking For:
- Medical Degree: MD, DO, MBBS, or equivalent from an accredited medical program (currently enrolled candidates may also be considered).
- Clinical Experience: Hands-on experience in a healthcare setting; strong preference for practising or recently practising clinicians.
- Subject Mastery: Ability to develop and critique complex, graduate-level medical reasoning tasks.
- English Proficiency: Fluent in reading and writing, with minimal language errors.
- Analytical Skill: Detail-oriented with the ability to evaluate medical content for accuracy and logical flow.
Compensation & Terms:
- Base Rate: Up to 50/hour USD, depending on qualifications, location, project type, and performance.
- Location: Fully remote — available to candidates in supported geographies.
- Schedule: Fully flexible — work as much or as little as you’d like.
- Payouts: Weekly.
Apply Now!
This advertiser has chosen not to accept applicants from your region.
7
Healthcare Specialist (AI Training)
Delhi, Delhi
Taskify
Posted 5 days ago
Job Viewed
Job Description
We're Hiring Healthcare Specialist For AI Training (Remote) | Earn Between $5,000 - $,000/Month
About the Role: Are you a medical professional with a passion for advancing AI? We are seeking medical experts to contribute to the training and refinement of cutting-edge artificial intelligence models. In this fully remote and flexible role, you will leverage your clinical knowledge to enhance AI's ability to perform diagnostic and reasoning tasks with precision and accuracy.
Who Can Join?
Medical consultants
Students MBBS / Nursing / BDS / BPT / Allied Health
Health professionals, including doctors, nurses, physician assistants, and various allied health professionals like therapists, dietitians, and technicians, etc.
What You'll Do:
Create and answer complex clinical questions to train AI in diagnostic and reasoning tasks.
Review and analyse AI model responses for clinical soundness, scientific rigour, and relevance.
Rank and assess AI outputs to identify strengths, weaknesses, and opportunities for improvement.
Provide expert feedback to help improve the quality, accuracy, and logic of AI-generated content.
You may be assigned to different projects based on your expertise and performance.
What We're Looking For:
Medical Degree: MD, DO, MBBS, or equivalent from an accredited medical program (currently enrolled candidates may also be considered).
Clinical Experience: Hands-on experience in a healthcare setting; strong preference for practising or recently practising clinicians.
Subject Mastery: Ability to develop and critique complex, graduate-level medical reasoning tasks.
English Proficiency: Fluent in reading and writing, with minimal language errors.
Analytical Skill: Detail-oriented with the ability to evaluate medical content for accuracy and logical flow.
Compensation & Terms:
Base Rate: Up to 50/hour USD, depending on qualifications, location, project type, and performance.
Location: Fully remote — available to candidates in supported geographies.
Schedule: Fully flexible — work as much or as little as you’d like.
Payouts: Weekly.
Apply Now!
About the Role: Are you a medical professional with a passion for advancing AI? We are seeking medical experts to contribute to the training and refinement of cutting-edge artificial intelligence models. In this fully remote and flexible role, you will leverage your clinical knowledge to enhance AI's ability to perform diagnostic and reasoning tasks with precision and accuracy.
Who Can Join?
Medical consultants
Students MBBS / Nursing / BDS / BPT / Allied Health
Health professionals, including doctors, nurses, physician assistants, and various allied health professionals like therapists, dietitians, and technicians, etc.
What You'll Do:
Create and answer complex clinical questions to train AI in diagnostic and reasoning tasks.
Review and analyse AI model responses for clinical soundness, scientific rigour, and relevance.
Rank and assess AI outputs to identify strengths, weaknesses, and opportunities for improvement.
Provide expert feedback to help improve the quality, accuracy, and logic of AI-generated content.
You may be assigned to different projects based on your expertise and performance.
What We're Looking For:
Medical Degree: MD, DO, MBBS, or equivalent from an accredited medical program (currently enrolled candidates may also be considered).
Clinical Experience: Hands-on experience in a healthcare setting; strong preference for practising or recently practising clinicians.
Subject Mastery: Ability to develop and critique complex, graduate-level medical reasoning tasks.
English Proficiency: Fluent in reading and writing, with minimal language errors.
Analytical Skill: Detail-oriented with the ability to evaluate medical content for accuracy and logical flow.
Compensation & Terms:
Base Rate: Up to 50/hour USD, depending on qualifications, location, project type, and performance.
Location: Fully remote — available to candidates in supported geographies.
Schedule: Fully flexible — work as much or as little as you’d like.
Payouts: Weekly.
Apply Now!
This advertiser has chosen not to accept applicants from your region.
8
Healthcare Specialist (AI Training)
Davangere, Karnataka
Taskify
Posted today
Job Viewed
Job Description
We're Hiring Healthcare Specialist For AI Training (Remote) | Earn Between $5,000 - $,000/Month
About the Role: Are you a medical professional with a passion for advancing AI? We are seeking medical experts to contribute to the training and refinement of cutting-edge artificial intelligence models. In this fully remote and flexible role, you will leverage your clinical knowledge to enhance AI's ability to perform diagnostic and reasoning tasks with precision and accuracy.
Who Can Join?
- Medical consultants
- Students MBBS / Nursing / BDS / BPT / Allied Health
- Health professionals, including doctors, nurses, physician assistants, and various allied health professionals like therapists, dietitians, and technicians, etc.
What You'll Do:
- Create and answer complex clinical questions to train AI in diagnostic and reasoning tasks.
- Review and analyse AI model responses for clinical soundness, scientific rigour, and relevance.
- Rank and assess AI outputs to identify strengths, weaknesses, and opportunities for improvement.
- Provide expert feedback to help improve the quality, accuracy, and logic of AI-generated content.
- You may be assigned to different projects based on your expertise and performance.
What We're Looking For:
- Medical Degree: MD, DO, MBBS, or equivalent from an accredited medical program (currently enrolled candidates may also be considered).
- Clinical Experience: Hands-on experience in a healthcare setting; strong preference for practising or recently practising clinicians.
- Subject Mastery: Ability to develop and critique complex, graduate-level medical reasoning tasks.
- English Proficiency: Fluent in reading and writing, with minimal language errors.
- Analytical Skill: Detail-oriented with the ability to evaluate medical content for accuracy and logical flow.
Compensation & Terms:
- Base Rate: Up to 50/hour USD, depending on qualifications, location, project type, and performance.
- Location: Fully remote — available to candidates in supported geographies.
- Schedule: Fully flexible — work as much or as little as you’d like.
- Payouts: Weekly.
Apply Now!
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