182 Fieldwork jobs in India

The Quantitative Fieldwork Coordinator assists the Client Service team with day-to-day management of market research studies, to ensure all projects successfully complete on time, within the budget and in accordance with the project specifications, while meeting and exceeding client expectations.

The Fieldwork Coordinator is one of the key team members in the execution of the quantitative project, and is responsible for field management and sample strategies, and will be accountable for coordinating with respondents, vendors, and clients. They will assist with the set-up of the study and other project requirements as needed.

Essential Duties and Responsibilities:

The Fieldwork Coordinator responsibilities listed below are inclusive but not limited to

Project Execution:

• Manage end-to-end project tasks including (but not limited to): link setup and testing, language requests, desk research, quality and audit checks, study invitation setup, deployment of sample, exclusion list management, M3 Wallet approvals, preparation for invoicing, and cost reconciliation.
• Build, update, and track sample plans based on screener specifications.

Fieldwork Coordination:

• Host pretest/pilot interviews for clients, ensuring they are conducted on time and as planned.
• Proactively identify and implement alternative fieldwork strategies to improve response rates and manage costs.
• Monitor and manage partners on quantitative projects throughout the project lifecycle to ensure client expectations are met or exceeded.
• Alert Project Managers when fieldwork strategies are underperforming, timelines are at risk, or quality concerns arise, and collaborate on solutions.
• Coordinate recruitment with supporting team such as Custom Recruitment team and Phone team.
• Submit requests for multichannel recruitment methodologies, including (but not limited to): email campaigns, phone outreach, desk research, SMS, online ads, referral programs, forums, blogs, patient groups, associations, and social media.

Project Closure:

• Send final updates and cost summaries to partners before invoice issuance.
• Track, monitor, and report on sampling performance and project costs to support gross profit improvement and timely delivery.
• Assist Project Managers with invoicing to ensure projects are closed and ready for billing promptly.

Collaboration & Communication:

• Attend project meetings with Project Managers to ensure alignment on specifications, client needs, timelines, and responsibilities.
• Take notes during briefings and meetings and share summaries with attendees.
• Address requests from the Support Team and other stakeholders in a timely manner.
• Partner with Project Managers, Senior Project Managers, and Project Directors to support day-to-day project needs, including administrative tasks and fieldwork planning.

• Bachelor's degree or equivalent required.
• Relevant coursework in market research or healthcare preferred but not required.
• 0 – 1 year of market research experience.
• Exceptional written and verbal communication skills, with demonstrated knowledge of English grammar rules.
• Strong Microsoft Office skills (Excel) and quick learner of new technologies/software.
• Must have basic math skills, with the ability to calculate incidence rate, response rates profit, etc.
• Interest / natural curiosity or previous experience /exposure within the healthcare space.
• Exhibit strong critical thinking skills and take initiative to improve skills and troubleshoot proactively with PM using all available resources to support project success.
• Ability to work autonomously and in a team environment to successfully meet study specific and departmental objectives.
• Self-motivated and able to (re)prioritize tasks throughout the workday.
• Exceptional time management, organizational skills, attention to detail and ability to multitask.

Willing to work in US EST hours or UK hours.

#LI-SA1
#LI-Remote

Job Location : Dholka, Near to Ahmedabad, Gujarat

About the Company :

Company : Cadila Pharmaceutical Ltd.

About Us : Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world.

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.

About the Role :

To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.

Responsibilities :

• To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
• Technology transfer of developed products to plant level, this includes all TTD-related works.
• To collect and compile all data and submit to respective regulatory agencies.
• To address DCGI/ regulatory agency queries as per requirement.
• To extend support to plant for any commercial trouble shooting.

Qualifications :

Ph/D

Required Skills :

• Formulation Development (solid oral dosage forms: tablets, capsules)
• Pre-formulation Studies
• Bioequivalence Study Design & Evaluation
• Technology Transfer (TTD)
• Scale-Up and Commercialization
• Analytical Data Interpretation
• Process Optimization & Troubleshooting
• Stability Studies (ICH Guidelines)
• Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)
• Quality by Design (QbD)

Preferred Skills :

Hands-on Experience with Formulation and Development

Pay range and compensation package :

8 LPA to 12 LPA

Job Location : Dholka, Near to Ahmedabad, Gujarat

About the Company :

Company: Cadila Pharmaceutical Ltd.

About Us: Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world.

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.

About the Role :

To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.

Responsibilities :

• To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
• Technology transfer of developed products to plant level, this includes all TTD-related works.
• To collect and compile all data and submit to respective regulatory agencies.
• To address DCGI/ regulatory agency queries as per requirement.
• To extend support to plant for any commercial trouble shooting.

Qualifications :

Ph/D

Required Skills :

• Formulation Development (solid oral dosage forms: tablets, capsules)
• Pre-formulation Studies
• Bioequivalence Study Design & Evaluation
• Technology Transfer (TTD)
• Scale-Up and Commercialization
• Analytical Data Interpretation
• Process Optimization & Troubleshooting
• Stability Studies (ICH Guidelines)
• Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)
• Quality by Design (QbD)

Preferred Skills :

Hands-on Experience with Formulation and Development

Pay range and compensation package :

8 LPA to 12 LPA

The International Potato Center (CIP) is a global,non-profit research organization that works to improve food security, nutrition, and incomes in developing countries through research and innovation in root and tuber crops—primarily potatoes and sweet potatoes .

CIP’s focus areas encompass a range of strategic priorities aimed at improving agricultural systems and livelihoods. These include crop improvement through the development of climate-resilient, high-yielding, and disease-resistant varieties of potatoes and sweet potatoes; sustainable farming by promoting environmentally friendly and resource-efficient agricultural practices; and nutrition and food systems , particularly through the use of biofortified crops. CIP also works to strengthen value chains and market access by supporting smallholder farmers in building inclusive and profitable value chains, while enhancing climate resilience by helping farming systems adapt to the impacts of climate change.

The International Potato Center (CIP) is seeking to recruit a highly motivated, field-oriented, and experienced Research Assistant to support a dynamic potato development initiative in South-West Haryana. The successful candidate will be based in Mahendragarh, Haryana and will be responsible for coordinating, implementing, and monitoring field-level agronomic activities across five districts.

This position offers an excellent opportunity to contribute to impactful agricultural research and development aimed at improving food security and livelihoods in the region.

The position requires a strong background in potato seed systems and agricultural practices. Practical expertise in pot-harvest management, pest and disease management, and potato production is essential. The candidate should also demonstrate the ability to prepare and disseminate technical reports, success stories, and promotional materials effectively.

The role includes strategic thinking and the ability to work collaboratively with farmers, government departments and internal project teams. While the role will primarily focus on agronomic duties, the selected candidate will also be expected to take on a wide range of responsibilities ensuring flexible and effective execution of activities as per project needs. Practical expertise in seed storage, pest and disease management, and potato production is essential. The candidate should also demonstrate the ability to prepare and disseminate technical reports, success stories, and promotional materials effectively.

Language: The candidate must be fluent in Hindi to conversate with farmers, with advanced written and oral communication skills in English.

Job Location : Dholka, Near to Ahmedabad, Gujarat

About the Company :

Company : Cadila Pharmaceutical Ltd.

About Us : Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world.

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.

About the Role :

To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.

Responsibilities :

• To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
• Technology transfer of developed products to plant level, this includes all TTD-related works.
• To collect and compile all data and submit to respective regulatory agencies.
• To address DCGI/ regulatory agency queries as per requirement.
• To extend support to plant for any commercial trouble shooting.

Qualifications :

Ph/D

Required Skills :

• Formulation Development (solid oral dosage forms: tablets, capsules)
• Pre-formulation Studies
• Bioequivalence Study Design & Evaluation
• Technology Transfer (TTD)
• Scale-Up and Commercialization
• Analytical Data Interpretation
• Process Optimization & Troubleshooting
• Stability Studies (ICH Guidelines)
• Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)
• Quality by Design (QbD)

Preferred Skills :

Hands-on Experience with Formulation and Development

Pay range and compensation package :

8 LPA to 12 LPA

Job Location : Dholka, Near to Ahmedabad, Gujarat

About the Company :

Company : Cadila Pharmaceutical Ltd.

About Us : Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world.

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.

About the Role :

To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.

Responsibilities :

• To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
• Technology transfer of developed products to plant level, this includes all TTD-related works.
• To collect and compile all data and submit to respective regulatory agencies.
• To address DCGI/ regulatory agency queries as per requirement.
• To extend support to plant for any commercial trouble shooting.

Qualifications :

Ph/D

Required Skills :

• Formulation Development (solid oral dosage forms: tablets, capsules)
• Pre-formulation Studies
• Bioequivalence Study Design & Evaluation
• Technology Transfer (TTD)
• Scale-Up and Commercialization
• Analytical Data Interpretation
• Process Optimization & Troubleshooting
• Stability Studies (ICH Guidelines)
• Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)
• Quality by Design (QbD)

Preferred Skills :

Hands-on Experience with Formulation and Development

Pay range and compensation package :

8 LPA to 12 LPA

Job Location : Dholka, Near to Ahmedabad, Gujarat

About the Company :

Company : Cadila Pharmaceutical Ltd.

About Us : Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world.

Our innovation- led drug discovery processes ensure the health and well-being of people around the world. Our enhanced investment in innovation and strong track record in research and development have produced medical miracles that have changed lives and made a profound impact on real life.

Being a care-focused, research-driven company, we are committed to complying with the highest ethical standards in the clinical research and medical practice. We lead our industry in demonstrating the application of cutting edge research to ethical business practices in producing the alchemy of optimum health outcomes for all.

About the Role :

To leverage my expertise in formulation development and regulatory compliance to develop stable and bioequivalent solid oral dosage forms for global markets, ensure successful technology transfer to manufacturing facilities, support regulatory submissions, address agency queries, and provide technical support for commercial production, contributing to the overall growth and compliance of the organization.

Responsibilities :

• To develop Stable and Bioequivalent solid oral products for US, Europe, ROW and Domestic Markets.
• Technology transfer of developed products to plant level, this includes all TTD-related works.
• To collect and compile all data and submit to respective regulatory agencies.
• To address DCGI/ regulatory agency queries as per requirement.
• To extend support to plant for any commercial trouble shooting.

Qualifications :

Ph/D

Required Skills :

• Formulation Development (solid oral dosage forms: tablets, capsules)
• Pre-formulation Studies
• Bioequivalence Study Design & Evaluation
• Technology Transfer (TTD)
• Scale-Up and Commercialization
• Analytical Data Interpretation
• Process Optimization & Troubleshooting
• Stability Studies (ICH Guidelines)
• Equipment Handling (e.g., granulators, blenders, tablet press, coating machines)
• Quality by Design (QbD)

Preferred Skills :

Hands-on Experience with Formulation and Development

Pay range and compensation package :

8 LPA to 12 LPA