181 Treatment Plans jobs in India
Research Associate in Max Institute of Healthcare Management
Posted 1 day ago
Job Viewed
Job Description
Job Purpose
Responsible for developing and overseeing trial protocols, coordinating data collection, and supporting the team in other research activities such as data cleaning, analysis, and writing manuscripts.
Job Outline
The Research Associate position provides an excellent opportunity to gain extensive hands‐on field research experience and significant management responsibility in a Tuberculosis care-related project.
The Research Associate will be responsible for (i) overseeing the implementation of trial protocols, (ii) overseeing collection of program data, (iii) training and managing survey teams, (iv) supervising logistics for field activities, (v) cleaning and analyzing survey data, (vi) assisting in the writing of project reports and policy memos,(vii) liaising with key government stakeholders and (viii) Monitoring and reviewing databases and rectifying errors or inconsistencies. The work will enhance your analytical and management skills and require your full commitment in a challenging environment.
About the project : A randomized control trial funded by The Bill and Melinda Gates Foundation to study
the impact of different digital adherence monitoring technologies (such as 99DOTS and MERM) deployed by the National TB program. The primary objective is to study how these monitoring methods impact patient adherence and clinical outcomes. The trial will involve the implementation of specific interventions, develop tools for primary data (interviews), and collect secondary programmatic data to estimate the impact of the interventions. Qualitative research will be conducted integrating all data sources to understand and explain the behavioral mechanisms driving impact and how to optimize interventions for patients and the health system. In addition, the study will also incorporate a Costing exercise and a Time-and-Motion study to estimate the cost and resource requirements of implementing different adherence technologies.
Job Specification
Knowledge / Education
- Master’s degree in public health/economics / public policy/epidemiology / development studies/management with healthcare sector experience
- Graduates from other disciplines may also be considered if they have relevant experience and can demonstrate the relevant skills
Specific Skills
- Excellent project management and organizational skills
- Meticulous attention to detail
- Ability to plan tasks for teams, monitor progress, make corrections to plans
- Strong budget management skills required
- Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices
- Capability to manage multiple tasks efficiently
- Must be able to work under pressure and meet deadlines, while maintaining a positive attitude
- Excellent verbal and written communication skills in (1) English, and (2) Hindi (3) Working knowledge of Punjabi desirable for Punjab location.
- Strong knowledge of MS Excel required; programming and other technical knowledge is a strong plus
- Demonstrated ability to manage relationships with partner organizations
- Willingness to frequently travel within study site
Desirable Experience
1. At least 2 years of work experience, preferably in healthcare
2. Candidates with prior experience with randomized controlled trials will be given strong preference
Job Interface/Relationships:
Internal
- MIHM Research and Admin team
- Other departments including Grants, Finance, Legal, and IT.
External
- Grantor research/programme team
- Vendors & Consultants
- Sub-grantees/data collection agencies
- IRB Boards, governments, other stakeholders
Key Responsibilities
- Develop and oversee compliance with RCT protocols
- Designing and implementing data quality assurance systems and protocols to ensure high-quality data collection
- Coordinating with internal and external stakeholders and supervising the data collection team to ensure smooth running of the trial
- Training, and managing the data collection team that will conduct the data collections
- Work with data sets, cleaning and running checks to spot errors, and generally preparing data for analysis using MS Excel
- Support the research team to analyze the data and interpret the findings
- Support in writing progress reports and other outputs
- Manage the budget including tracking all expenses to ensure costs are within project funds
Any Other Significant Input
Send an email to with the subject line “Application for Research Associate 2025” with a copy of your CV and academic transcripts. Any evidence of written work and references by academics would be a strong positive. Applications will be reviewed until the position is filled. You will be contacted only in case you are shortlisted for an interview.
Research Associate in Max Institute of Healthcare Management
Posted today
Job Viewed
Job Description
Responsible for developing and overseeing trial protocols, coordinating data collection, and supporting the team in other research activities such as data cleaning, analysis, and writing manuscripts.
Job Outline
The Research Associate position provides an excellent opportunity to gain extensive hands‐on field research experience and significant management responsibility in a Tuberculosis care-related project.
The Research Associate will be responsible for (i) overseeing the implementation of trial protocols, (ii) overseeing collection of program data, (iii) training and managing survey teams, (iv) supervising logistics for field activities, (v) cleaning and analyzing survey data, (vi) assisting in the writing of project reports and policy memos,(vii) liaising with key government stakeholders and (viii) Monitoring and reviewing databases and rectifying errors or inconsistencies. The work will enhance your analytical and management skills and require your full commitment in a challenging environment.
About the project : A randomized control trial funded by The Bill and Melinda Gates Foundation to study
the impact of different digital adherence monitoring technologies (such as 99DOTS and MERM) deployed by the National TB program. The primary objective is to study how these monitoring methods impact patient adherence and clinical outcomes. The trial will involve the implementation of specific interventions, develop tools for primary data (interviews), and collect secondary programmatic data to estimate the impact of the interventions. Qualitative research will be conducted integrating all data sources to understand and explain the behavioral mechanisms driving impact and how to optimize interventions for patients and the health system. In addition, the study will also incorporate a Costing exercise and a Time-and-Motion study to estimate the cost and resource requirements of implementing different adherence technologies.
Job Specification
Knowledge / Education
Master’s degree in public health/economics / public policy/epidemiology / development studies/management with healthcare sector experience
Graduates from other disciplines may also be considered if they have relevant experience and can demonstrate the relevant skills
Specific Skills
Excellent project management and organizational skills
Meticulous attention to detail
Ability to plan tasks for teams, monitor progress, make corrections to plans
Strong budget management skills required
Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices
Capability to manage multiple tasks efficiently
Must be able to work under pressure and meet deadlines, while maintaining a positive attitude
Excellent verbal and written communication skills in (1) English, and (2) Hindi (3) Working knowledge of Punjabi desirable for Punjab location.
Strong knowledge of MS Excel required; programming and other technical knowledge is a strong plus
Demonstrated ability to manage relationships with partner organizations
Willingness to frequently travel within study site
Desirable Experience
1. At least 2 years of work experience, preferably in healthcare
2. Candidates with prior experience with randomized controlled trials will be given strong preference
Job Interface/Relationships:
Internal
MIHM Research and Admin team
Other departments including Grants, Finance, Legal, and IT.
External
Grantor research/programme team
Vendors & Consultants
Sub-grantees/data collection agencies
IRB Boards, governments, other stakeholders
Key Responsibilities
Develop and oversee compliance with RCT protocols
Designing and implementing data quality assurance systems and protocols to ensure high-quality data collection
Coordinating with internal and external stakeholders and supervising the data collection team to ensure smooth running of the trial
Training, and managing the data collection team that will conduct the data collections
Work with data sets, cleaning and running checks to spot errors, and generally preparing data for analysis using MS Excel
Support the research team to analyze the data and interpret the findings
Support in writing progress reports and other outputs
Manage the budget including tracking all expenses to ensure costs are within project funds
Any Other Significant Input
Send an email to with the subject line “Application for Research Associate 2025” with a copy of your CV and academic transcripts. Any evidence of written work and references by academics would be a strong positive. Applications will be reviewed until the position is filled. You will be contacted only in case you are shortlisted for an interview.
Research Associate in Max Institute of Healthcare Management
Posted today
Job Viewed
Job Description
Job Purpose
Responsible for developing and overseeing trial protocols, coordinating data collection, and supporting the team in other research activities such as data cleaning, analysis, and writing manuscripts.
Job Outline
The Research Associate position provides an excellent opportunity to gain extensive hands‐on field research experience and significant management responsibility in a Tuberculosis care-related project.
The Research Associate will be responsible for (i) overseeing the implementation of trial protocols, (ii) overseeing collection of program data, (iii) training and managing survey teams, (iv) supervising logistics for field activities, (v) cleaning and analyzing survey data, (vi) assisting in the writing of project reports and policy memos,(vii) liaising with key government stakeholders and (viii) Monitoring and reviewing databases and rectifying errors or inconsistencies. The work will enhance your analytical and management skills and require your full commitment in a challenging environment.
About the project : A randomized control trial funded by The Bill and Melinda Gates Foundation to study
the impact of different digital adherence monitoring technologies (such as 99DOTS and MERM) deployed by the National TB program. The primary objective is to study how these monitoring methods impact patient adherence and clinical outcomes. The trial will involve the implementation of specific interventions, develop tools for primary data (interviews), and collect secondary programmatic data to estimate the impact of the interventions. Qualitative research will be conducted integrating all data sources to understand and explain the behavioral mechanisms driving impact and how to optimize interventions for patients and the health system. In addition, the study will also incorporate a Costing exercise and a Time-and-Motion study to estimate the cost and resource requirements of implementing different adherence technologies.
Job Specification
Knowledge / Education
- Master’s degree in public health/economics / public policy/epidemiology / development studies/management with healthcare sector experience
- Graduates from other disciplines may also be considered if they have relevant experience and can demonstrate the relevant skills
Specific Skills
- Excellent project management and organizational skills
- Meticulous attention to detail
- Ability to plan tasks for teams, monitor progress, make corrections to plans
- Strong budget management skills required
- Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices
- Capability to manage multiple tasks efficiently
- Must be able to work under pressure and meet deadlines, while maintaining a positive attitude
- Excellent verbal and written communication skills in (1) English, and (2) Hindi (3) Working knowledge of Punjabi desirable for Punjab location.
- Strong knowledge of MS Excel required; programming and other technical knowledge is a strong plus
- Demonstrated ability to manage relationships with partner organizations
- Willingness to frequently travel within study site
Desirable Experience
1. At least 2 years of work experience, preferably in healthcare
2. Candidates with prior experience with randomized controlled trials will be given strong preference
Job Interface/Relationships:
Internal
- MIHM Research and Admin team
- Other departments including Grants, Finance, Legal, and IT.
External
- Grantor research/programme team
- Vendors & Consultants
- Sub-grantees/data collection agencies
- IRB Boards, governments, other stakeholders
Key Responsibilities
- Develop and oversee compliance with RCT protocols
- Designing and implementing data quality assurance systems and protocols to ensure high-quality data collection
- Coordinating with internal and external stakeholders and supervising the data collection team to ensure smooth running of the trial
- Training, and managing the data collection team that will conduct the data collections
- Work with data sets, cleaning and running checks to spot errors, and generally preparing data for analysis using MS Excel
- Support the research team to analyze the data and interpret the findings
- Support in writing progress reports and other outputs
- Manage the budget including tracking all expenses to ensure costs are within project funds
Any Other Significant Input
Send an email to with the subject line “Application for Research Associate 2025” with a copy of your CV and academic transcripts. Any evidence of written work and references by academics would be a strong positive. Applications will be reviewed until the position is filled. You will be contacted only in case you are shortlisted for an interview.
Research associate in max institute of healthcare management
Posted today
Job Viewed
Job Description
Research Associate in Max Institute of Healthcare Management
Posted today
Job Viewed
Job Description
Job Purpose
Responsible for developing and overseeing trial protocols, coordinating data collection, and supporting the team in other research activities such as data cleaning, analysis, and writing manuscripts.
Job Outline
The Research Associate position provides an excellent opportunity to gain extensive hands‐on field research experience and significant management responsibility in a Tuberculosis care-related project.
The Research Associate will be responsible for (i) overseeing the implementation of trial protocols, (ii) overseeing collection of program data, (iii) training and managing survey teams, (iv) supervising logistics for field activities, (v) cleaning and analyzing survey data, (vi) assisting in the writing of project reports and policy memos,(vii) liaising with key government stakeholders and (viii) Monitoring and reviewing databases and rectifying errors or inconsistencies. The work will enhance your analytical and management skills and require your full commitment in a challenging environment.
About the project : A randomized control trial funded by The Bill and Melinda Gates Foundation to study
the impact of different digital adherence monitoring technologies (such as 99DOTS and MERM) deployed by the National TB program. The primary objective is to study how these monitoring methods impact patient adherence and clinical outcomes. The trial will involve the implementation of specific interventions, develop tools for primary data (interviews), and collect secondary programmatic data to estimate the impact of the interventions. Qualitative research will be conducted integrating all data sources to understand and explain the behavioral mechanisms driving impact and how to optimize interventions for patients and the health system. In addition, the study will also incorporate a Costing exercise and a Time-and-Motion study to estimate the cost and resource requirements of implementing different adherence technologies.
Job Specification
Knowledge / Education
- Master’s degree in public health/economics / public policy/epidemiology / development studies/management with healthcare sector experience
- Graduates from other disciplines may also be considered if they have relevant experience and can demonstrate the relevant skills
Specific Skills
- Excellent project management and organizational skills
- Meticulous attention to detail
- Ability to plan tasks for teams, monitor progress, make corrections to plans
- Strong budget management skills required
- Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices
- Capability to manage multiple tasks efficiently
- Must be able to work under pressure and meet deadlines, while maintaining a positive attitude
- Excellent verbal and written communication skills in (1) English, and (2) Hindi (3) Working knowledge of Punjabi desirable for Punjab location.
- Strong knowledge of MS Excel required; programming and other technical knowledge is a strong plus
- Demonstrated ability to manage relationships with partner organizations
- Willingness to frequently travel within study site
Desirable Experience
1. At least 2 years of work experience, preferably in healthcare
2. Candidates with prior experience with randomized controlled trials will be given strong preference
Job Interface/Relationships:
Internal
- MIHM Research and Admin team
- Other departments including Grants, Finance, Legal, and IT.
External
- Grantor research/programme team
- Vendors & Consultants
- Sub-grantees/data collection agencies
- IRB Boards, governments, other stakeholders
Key Responsibilities
- Develop and oversee compliance with RCT protocols
- Designing and implementing data quality assurance systems and protocols to ensure high-quality data collection
- Coordinating with internal and external stakeholders and supervising the data collection team to ensure smooth running of the trial
- Training, and managing the data collection team that will conduct the data collections
- Work with data sets, cleaning and running checks to spot errors, and generally preparing data for analysis using MS Excel
- Support the research team to analyze the data and interpret the findings
- Support in writing progress reports and other outputs
- Manage the budget including tracking all expenses to ensure costs are within project funds
Any Other Significant Input
Send an email to with the subject line “Application for Research Associate 2025” with a copy of your CV and academic transcripts. Any evidence of written work and references by academics would be a strong positive. Applications will be reviewed until the position is filled. You will be contacted only in case you are shortlisted for an interview.
Research Associate in Max Institute of Healthcare Management
Posted today
Job Viewed
Job Description
Job Purpose
Responsible for developing and overseeing trial protocols, coordinating data collection, and supporting the team in other research activities such as data cleaning, analysis, and writing manuscripts.
Job Outline
The Research Associate position provides an excellent opportunity to gain extensive hands‐on field research experience and significant management responsibility in a Tuberculosis care-related project.
The Research Associate will be responsible for (i) overseeing the implementation of trial protocols, (ii) overseeing collection of program data, (iii) training and managing survey teams, (iv) supervising logistics for field activities, (v) cleaning and analyzing survey data, (vi) assisting in the writing of project reports and policy memos,(vii) liaising with key government stakeholders and (viii) Monitoring and reviewing databases and rectifying errors or inconsistencies. The work will enhance your analytical and management skills and require your full commitment in a challenging environment.
About the project : A randomized control trial funded by The Bill and Melinda Gates Foundation to study
the impact of different digital adherence monitoring technologies (such as 99DOTS and MERM) deployed by the National TB program. The primary objective is to study how these monitoring methods impact patient adherence and clinical outcomes. The trial will involve the implementation of specific interventions, develop tools for primary data (interviews), and collect secondary programmatic data to estimate the impact of the interventions. Qualitative research will be conducted integrating all data sources to understand and explain the behavioral mechanisms driving impact and how to optimize interventions for patients and the health system. In addition, the study will also incorporate a Costing exercise and a Time-and-Motion study to estimate the cost and resource requirements of implementing different adherence technologies.
Job Specification
Knowledge / Education
- Master’s degree in public health/economics / public policy/epidemiology / development studies/management with healthcare sector experience
- Graduates from other disciplines may also be considered if they have relevant experience and can demonstrate the relevant skills
Specific Skills
- Excellent project management and organizational skills
- Meticulous attention to detail
- Ability to plan tasks for teams, monitor progress, make corrections to plans
- Strong budget management skills required
- Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices
- Capability to manage multiple tasks efficiently
- Must be able to work under pressure and meet deadlines, while maintaining a positive attitude
- Excellent verbal and written communication skills in (1) English, and (2) Hindi (3) Working knowledge of Punjabi desirable for Punjab location.
- Strong knowledge of MS Excel required; programming and other technical knowledge is a strong plus
- Demonstrated ability to manage relationships with partner organizations
- Willingness to frequently travel within study site
Desirable Experience
1. At least 2 years of work experience, preferably in healthcare
2. Candidates with prior experience with randomized controlled trials will be given strong preference
Job Interface/Relationships:
Internal
- MIHM Research and Admin team
- Other departments including Grants, Finance, Legal, and IT.
External
- Grantor research/programme team
- Vendors & Consultants
- Sub-grantees/data collection agencies
- IRB Boards, governments, other stakeholders
Key Responsibilities
- Develop and oversee compliance with RCT protocols
- Designing and implementing data quality assurance systems and protocols to ensure high-quality data collection
- Coordinating with internal and external stakeholders and supervising the data collection team to ensure smooth running of the trial
- Training, and managing the data collection team that will conduct the data collections
- Work with data sets, cleaning and running checks to spot errors, and generally preparing data for analysis using MS Excel
- Support the research team to analyze the data and interpret the findings
- Support in writing progress reports and other outputs
- Manage the budget including tracking all expenses to ensure costs are within project funds
Any Other Significant Input
Send an email to with the subject line “Application for Research Associate 2025” with a copy of your CV and academic transcripts. Any evidence of written work and references by academics would be a strong positive. Applications will be reviewed until the position is filled. You will be contacted only in case you are shortlisted for an interview.
Research Associate in Max Institute of Healthcare Management
Posted 9 days ago
Job Viewed
Job Description
Job Purpose
Responsible for developing and overseeing trial protocols, coordinating data collection, and supporting the team in other research activities such as data cleaning, analysis, and writing manuscripts.
Job Outline
The Research Associate position provides an excellent opportunity to gain extensive hands‐on field research experience and significant management responsibility in a Tuberculosis care-related project.
The Research Associate will be responsible for (i) overseeing the implementation of trial protocols, (ii) overseeing collection of program data, (iii) training and managing survey teams, (iv) supervising logistics for field activities, (v) cleaning and analyzing survey data, (vi) assisting in the writing of project reports and policy memos,(vii) liaising with key government stakeholders and (viii) Monitoring and reviewing databases and rectifying errors or inconsistencies. The work will enhance your analytical and management skills and require your full commitment in a challenging environment.
About the project : A randomized control trial funded by The Bill and Melinda Gates Foundation to study
the impact of different digital adherence monitoring technologies (such as 99DOTS and MERM) deployed by the National TB program. The primary objective is to study how these monitoring methods impact patient adherence and clinical outcomes. The trial will involve the implementation of specific interventions, develop tools for primary data (interviews), and collect secondary programmatic data to estimate the impact of the interventions. Qualitative research will be conducted integrating all data sources to understand and explain the behavioral mechanisms driving impact and how to optimize interventions for patients and the health system. In addition, the study will also incorporate a Costing exercise and a Time-and-Motion study to estimate the cost and resource requirements of implementing different adherence technologies.
Job Specification
Knowledge / Education
- Master’s degree in public health/economics / public policy/epidemiology / development studies/management with healthcare sector experience
- Graduates from other disciplines may also be considered if they have relevant experience and can demonstrate the relevant skills
Specific Skills
- Excellent project management and organizational skills
- Meticulous attention to detail
- Ability to plan tasks for teams, monitor progress, make corrections to plans
- Strong budget management skills required
- Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices
- Capability to manage multiple tasks efficiently
- Must be able to work under pressure and meet deadlines, while maintaining a positive attitude
- Excellent verbal and written communication skills in (1) English, and (2) Hindi (3) Working knowledge of Punjabi desirable for Punjab location.
- Strong knowledge of MS Excel required; programming and other technical knowledge is a strong plus
- Demonstrated ability to manage relationships with partner organizations
- Willingness to frequently travel within study site
Desirable Experience
1. At least 2 years of work experience, preferably in healthcare
2. Candidates with prior experience with randomized controlled trials will be given strong preference
Job Interface/Relationships:
Internal
- MIHM Research and Admin team
- Other departments including Grants, Finance, Legal, and IT.
External
- Grantor research/programme team
- Vendors & Consultants
- Sub-grantees/data collection agencies
- IRB Boards, governments, other stakeholders
Key Responsibilities
- Develop and oversee compliance with RCT protocols
- Designing and implementing data quality assurance systems and protocols to ensure high-quality data collection
- Coordinating with internal and external stakeholders and supervising the data collection team to ensure smooth running of the trial
- Training, and managing the data collection team that will conduct the data collections
- Work with data sets, cleaning and running checks to spot errors, and generally preparing data for analysis using MS Excel
- Support the research team to analyze the data and interpret the findings
- Support in writing progress reports and other outputs
- Manage the budget including tracking all expenses to ensure costs are within project funds
Any Other Significant Input
Send an email to with the subject line “Application for Research Associate 2025” with a copy of your CV and academic transcripts. Any evidence of written work and references by academics would be a strong positive. Applications will be reviewed until the position is filled. You will be contacted only in case you are shortlisted for an interview.
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Research Associate In Max Institute Of Healthcare Management
Posted today
Job Viewed
Job Description
Job Purpose
Responsible for developing and overseeing trial protocols, coordinating data collection, and supporting the team in other research activities such as data cleaning, analysis, and writing manuscripts.
Job Outline
The Research Associate position provides an excellent opportunity to gain extensive hands‐on field research experience and significant management responsibility in a Tuberculosis care-related project.
The Research Associate will be responsible for (i) overseeing the implementation of trial protocols, (ii) overseeing collection of program data, (iii) training and managing survey teams, (iv) supervising logistics for field activities, (v) cleaning and analyzing survey data, (vi) assisting in the writing of project reports and policy memos,(vii) liaising with key government stakeholders and (viii) Monitoring and reviewing databases and rectifying errors or inconsistencies. The work will enhance your analytical and management skills and require your full commitment in a challenging environment.
About the project : A randomized control trial funded by The Bill and Melinda Gates Foundation to study
the impact of different digital adherence monitoring technologies (such as 99DOTS and MERM) deployed by the National TB program. The primary objective is to study how these monitoring methods impact patient adherence and clinical outcomes. The trial will involve the implementation of specific interventions, develop tools for primary data (interviews), and collect secondary programmatic data to estimate the impact of the interventions. Qualitative research will be conducted integrating all data sources to understand and explain the behavioral mechanisms driving impact and how to optimize interventions for patients and the health system. In addition, the study will also incorporate a Costing exercise and a Time-and-Motion study to estimate the cost and resource requirements of implementing different adherence technologies.
Job Specification
Knowledge / Education
- Master’s degree in public health/economics / public policy/epidemiology / development studies/management with healthcare sector experience
- Graduates from other disciplines may also be considered if they have relevant experience and can demonstrate the relevant skills
Specific Skills
- Excellent project management and organizational skills
- Meticulous attention to detail
- Ability to plan tasks for teams, monitor progress, make corrections to plans
- Strong budget management skills required
- Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices
- Capability to manage multiple tasks efficiently
- Must be able to work under pressure and meet deadlines, while maintaining a positive attitude
- Excellent verbal and written communication skills in (1) English, and (2) Hindi (3) Working knowledge of Punjabi desirable for Punjab location.
- Strong knowledge of MS Excel required;
programming and other technical knowledge is a strong plus - Demonstrated ability to manage relationships with partner organizations
- Willingness to frequently travel within study site
Desirable Experience
1. At least 2 years of work experience, preferably in healthcare
2. Candidates with prior experience with randomized controlled trials will be given strong preference
Job Interface/Relationships:
Internal
- MIHM Research and Admin team
- Other departments including Grants, Finance, Legal, and IT.
External
- Grantor research/programme team
- Vendors & Consultants
- Sub-grantees/data collection agencies
- IRB Boards, governments, other stakeholders
Key Responsibilities
- Develop and oversee compliance with RCT protocols
- Designing and implementing data quality assurance systems and protocols to ensure high-quality data collection
- Coordinating with internal and external stakeholders and supervising the data collection team to ensure smooth running of the trial
- Training, and managing the data collection team that will conduct the data collections
- Work with data sets, cleaning and running checks to spot errors, and generally preparing data for analysis using MS Excel
- Support the research team to analyze the data and interpret the findings
- Support in writing progress reports and other outputs
- Manage the budget including tracking all expenses to ensure costs are within project funds
Any Other Significant Input
Send an email to with the subject line “Application for Research Associate 2025” with a copy of your CV and academic transcripts. Any evidence of written work and references by academics would be a strong positive. Applications will be reviewed until the position is filled. You will be contacted only in case you are shortlisted for an interview.
Patient Care Coordinator
Posted 1 day ago
Job Viewed
Job Description
Company Description
SKS Veterinary Hospital and Pet Shop provide centers of excellence in cardiology, oncology, orthopaedic surgery, gastroenterology, GI surgery, ophthalmology, radiology, urology, dental care, laboratory, and pediatric care. In addition to immunization and treatments, we offer services such as pet boarding and routine and medicated bathing. Our hospital also carries a wide variety of prescription diets, flea/tick control products, and heartworm preventatives for your pet's overall health.
Role Description
This is a full-time on-site role for a Patient Care Coordinator located in Chennai (Abiramapuram). The Pet Parent - Patient Care Coordinator will be responsible for scheduling appointments, managing patient care, coordinating various healthcare services, ensuring efficient communication between patients and healthcare providers, and handling phone inquiries with professionalism. The role requires knowledge of medical terminology and an ability to provide excellent patient care.
Morning and Noon Shift will be there
Qualifications
- Appointment Scheduling and Care Coordination skills
- Phone Etiquette and Patient Care skills
- Knowledge of Medical Terminology
- Strong organizational and multitasking abilities
- Excellent communication and interpersonal skills
- Previous experience in a veterinary or healthcare setting is a plus
- Multi lingual ( Tamil, English and Hindi)
Job Type: Full-time
Pay: ₹15,000.00 - ₹25,000.00 per month
Patient Care Coordinator
Posted today
Job Viewed
Job Description
*Ensure confidentiality at all times
* Maintain accurate records & reports
* Coordinate patient care from admission to discharge
* Manage patient counseling sessions
* HR training and performance
* Coordination in depts
Office cab/shuttle
Provident fund