20 Icmr jobs in India
Project Research Scientist-i (Non- Medical)
Posted today
Job Viewed
Job Description
**Funding Agency**: ICMR, Department of Health Research Mo&HFW.
**Principal Investigator**: Dr. Jeyaraj Durai Pandian, Professor of Neurology and Principal (Dean) Christian Medical College, Ludhiana
**Place of Posting: Ludhiana**: District of Punjab
**Essential Qulaification**:BDS/BPT/BAMS/BHMS + Post Graduate Degree, Including the integrated PG Degree with three years experience or MPH/PHD
**Desirable Experience**:
(a) Prior experience in public health programs including working with national/ State government, especially with NHM, Universal Health coverage, etc;
b) Prior experience in Non-Communicable diseases and Health system strengthening is desirable;
c)Experience in providing technical assistance related to strengthening institutional and individual capacity in health systems at all levels as well as pre-hospital systems;
d)Demonstrated experience in writing technical reports and proposals, publications, making PPTs for presentations to state/ national health authorities
**Skills and Competencies**:
a) Demonstrated ability to design, implement, and drive change in large program settings.
B) Strong collaboration skills and ability & work with diverse teams.
C) Excellent skills in oral and written communication.
d) Excellent knowledge of Microsoft Application.
Pay: ₹25,000.00 - ₹35,000.00 per month
**Benefits**:
- Leave encashment
- Provident Fund
Schedule:
- Day shift
- Morning shift
- Weekend availability
Supplemental Pay:
- Performance bonus
- Shift allowance
Ability to commute/relocate:
- Ludhiana, Punjab: Reliably commute or planning to relocate before starting work (required)
**Experience**:
- total work: 1 year (preferred)
Work Location: In person
Jobs For Clinical Research Associate-Medical & Clinical Industry-Hyderabad, Telangana, India-4 La...
Posted today
Job Viewed
Job Description
JOB DETAILS
1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.
2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.
3. Review informed consent document / procedures.
4. Negotiate study budgets with potential investigators and assists with the execution of site contracts Provide monitoring visits and site management for a variety of protocols, sites
5. Administer protocol and other study-related training to assigned site personnel and establish regular lines of communication with the sites to manage ongoing project expectations and issues.
6. Evaluate the quality and integrity of the practices of the study site related to the proper conduct of the protocol and adherence to applicable regulations.
7. Escalate quality issues to the CPM / line manager, as deemed necessary.
8. Ensure accurate data reporting via review of site source documents and medical records.
9. Interpret data to identify protocol deviations and risks to subject safety/data integrity.
10. Perform investigational product accountability as per the protocol and Study Monitoring Plan.
FUNCTIONAL AREA
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Director of Regulatory Research & Intelligence – India (Pharmaceutical & Medical Devices)
Posted 1 day ago
Job Viewed
Job Description
Job Title: Director of Regulatory Research & Intelligence
Location: Hybrid (Hyderabad)
Industry: Life Sciences / Healthcare Technology
Experience Level: 10+ years
Employment Type: Full-time
About the Role
Kamet Consulting Group is seeking a high-impact Director to lead our Global Regulatory Research & Intelligence function while driving strategic business development and market penetration. This dual-role leader will oversee a high-performing research intelligence team and own commercial growth initiatives, leveraging regulatory expertise to win new business, deepen client relationships, and expand our footprint in priority geographies.
The ideal candidate brings proven quota achievement over their tenure, deep knowledge of global regulatory frameworks, and the ability to translate regulatory insight into competitive advantage and revenue growth.
Core Responsibilities
· Regulatory Leadership & Intelligence Oversight
- Lead, mentor, and grow a multidisciplinary Regulatory Research & Intelligence team; set clear performance, quality, and delivery metrics.
- Define and evolve research agendas aligned to emerging regulatory trends (FDA, EMA, CDSCO, TGA, WHO, ICH, etc.) and client priorities.
- Oversee execution of complex regulatory intelligence projects—ensuring on-time, on-budget, and in-scope delivery.
- Serve as senior authority on regulatory intelligence, ensuring compliance with global quality standards and minimizing client risk.
- Present complex regulatory implications and recommendations to senior executives in clear, commercially relevant language.
Business Development & Market Penetration
- Develop and execute a go-to-market strategy to penetrate new regions and sectors within life sciences and healthcare technology.
- Leverage regulatory expertise to identify and secure high-value consulting, advisory, and outsourced service engagements.
- Own revenue targets and consistently achieve or exceed sales quotas through proactive pipeline building, solution selling, and account expansion.
- Partner with Leadership to position Kamet as a thought leader in global regulatory affairs.
- Negotiate and close complex, multi-year contracts with C-suite and senior decision-makers.
Cross-Functional Collaboration
- Collaborate closely with consultants, SMEs, and leadership across clinical, quality, supply chain, labeling, and M&A advisory services.
- Align business development activities with operational delivery to ensure client satisfaction and repeat engagements.
Required Qualifications
· Education: Advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or related field; PhD or MBA preferred. RAC or equivalent certification a plus.
· Experience:
- 10+ years in regulatory affairs, regulatory intelligence, or compliance within pharma/medical devices.
- 5+ years in consulting with direct client-facing and team leadership responsibilities.
- Proven track record of meeting or exceeding business development quotas and delivering measurable revenue growth.
· Regulatory Expertise: Mastery of global and Indian regulatory frameworks (FDA, EMA, CDSCO, WHO, ICH, GMP, GCP, QMS).
· Commercial Acumen: Skilled at identifying market opportunities, shaping client solutions, and closing strategic deals.
· Leadership: Demonstrated success in managing high-performance, multicultural teams.
· Communication: Exceptional English written and verbal skills with the ability to distill technical concepts for executive audiences.
Desired Traits
· Entrepreneurial, growth-oriented mindset with a balance of technical and commercial skills.
· Ability to operate seamlessly between strategic planning, operational oversight, and hands-on business development.
· High ethical standards and commitment to excellence in client delivery.
About Kamet Consulting Group
Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. We are an equal opportunity employer. All qualified applicants are encouraged to apply.
Why Join Us
- Contribute to meaningful technology in the life sciences domain.
- Work with a collaborative, forward-thinking team committed to innovation.
- Competitive compensation and benefits package.
- Flexible working arrangements and growth opportunities.
Director of Regulatory Research & Intelligence – India (Pharmaceutical & Medical Devices)
Posted today
Job Viewed
Job Description
Location: Hybrid (Hyderabad)
Industry: Life Sciences / Healthcare Technology
Experience Level: 10+ years
Employment Type: Full-time
About the Role
Kamet Consulting Group is seeking a high-impact Director to lead our Global Regulatory Research & Intelligence function while driving strategic business development and market penetration. This dual-role leader will oversee a high-performing research intelligence team and own commercial growth initiatives, leveraging regulatory expertise to win new business, deepen client relationships, and expand our footprint in priority geographies.
The ideal candidate brings proven quota achievement over their tenure, deep knowledge of global regulatory frameworks, and the ability to translate regulatory insight into competitive advantage and revenue growth.
Core Responsibilities
· Regulatory Leadership & Intelligence Oversight
- Lead, mentor, and grow a multidisciplinary Regulatory Research & Intelligence team; set clear performance, quality, and delivery metrics.
- Define and evolve research agendas aligned to emerging regulatory trends (FDA, EMA, CDSCO, TGA, WHO, ICH, etc.) and client priorities.
- Oversee execution of complex regulatory intelligence projects—ensuring on-time, on-budget, and in-scope delivery.
- Serve as senior authority on regulatory intelligence, ensuring compliance with global quality standards and minimizing client risk.
- Present complex regulatory implications and recommendations to senior executives in clear, commercially relevant language.
Business Development & Market Penetration
- Develop and execute a go-to-market strategy to penetrate new regions and sectors within life sciences and healthcare technology.
- Leverage regulatory expertise to identify and secure high-value consulting, advisory, and outsourced service engagements.
- Own revenue targets and consistently achieve or exceed sales quotas through proactive pipeline building, solution selling, and account expansion.
- Partner with Leadership to position Kamet as a thought leader in global regulatory affairs.
- Negotiate and close complex, multi-year contracts with C-suite and senior decision-makers.
Cross-Functional Collaboration
- Collaborate closely with consultants, SMEs, and leadership across clinical, quality, supply chain, labeling, and M&A advisory services.
- Align business development activities with operational delivery to ensure client satisfaction and repeat engagements.
Required Qualifications
· Education: Advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or related field; PhD or MBA preferred. RAC or equivalent certification a plus.
· Experience:
- 10+ years in regulatory affairs, regulatory intelligence, or compliance within pharma/medical devices.
- 5+ years in consulting with direct client-facing and team leadership responsibilities.
- Proven track record of meeting or exceeding business development quotas and delivering measurable revenue growth.
· Regulatory Expertise: Mastery of global and Indian regulatory frameworks (FDA, EMA, CDSCO, WHO, ICH, GMP, GCP, QMS).
· Commercial Acumen: Skilled at identifying market opportunities, shaping client solutions, and closing strategic deals.
· Leadership: Demonstrated success in managing high-performance, multicultural teams.
· Communication: Exceptional English written and verbal skills with the ability to distill technical concepts for executive audiences.
Desired Traits
· Entrepreneurial, growth-oriented mindset with a balance of technical and commercial skills.
· Ability to operate seamlessly between strategic planning, operational oversight, and hands-on business development.
· High ethical standards and commitment to excellence in client delivery.
About Kamet Consulting Group
Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. We are an equal opportunity employer. All qualified applicants are encouraged to apply.
Why Join Us
- Contribute to meaningful technology in the life sciences domain.
- Work with a collaborative, forward-thinking team committed to innovation.
- Competitive compensation and benefits package.
- Flexible working arrangements and growth opportunities.
Director of Regulatory Research & Intelligence – India (Pharmaceutical & Medical Devices)
Posted today
Job Viewed
Job Description
Job Title: Director of Regulatory Research & Intelligence
Location: Hybrid (Hyderabad)
Industry: Life Sciences / Healthcare Technology
Experience Level: 10+ years
Employment Type: Full-time
About the Role
Kamet Consulting Group is seeking a high-impact Director to lead our Global Regulatory Research & Intelligence function while driving strategic business development and market penetration. This dual-role leader will oversee a high-performing research intelligence team and own commercial growth initiatives, leveraging regulatory expertise to win new business, deepen client relationships, and expand our footprint in priority geographies.
The ideal candidate brings proven quota achievement over their tenure, deep knowledge of global regulatory frameworks, and the ability to translate regulatory insight into competitive advantage and revenue growth.
Core Responsibilities
· Regulatory Leadership & Intelligence Oversight
- Lead, mentor, and grow a multidisciplinary Regulatory Research & Intelligence team; set clear performance, quality, and delivery metrics.
- Define and evolve research agendas aligned to emerging regulatory trends (FDA, EMA, CDSCO, TGA, WHO, ICH, etc.) and client priorities.
- Oversee execution of complex regulatory intelligence projects—ensuring on-time, on-budget, and in-scope delivery.
- Serve as senior authority on regulatory intelligence, ensuring compliance with global quality standards and minimizing client risk.
- Present complex regulatory implications and recommendations to senior executives in clear, commercially relevant language.
Business Development & Market Penetration
- Develop and execute a go-to-market strategy to penetrate new regions and sectors within life sciences and healthcare technology.
- Leverage regulatory expertise to identify and secure high-value consulting, advisory, and outsourced service engagements.
- Own revenue targets and consistently achieve or exceed sales quotas through proactive pipeline building, solution selling, and account expansion.
- Partner with Leadership to position Kamet as a thought leader in global regulatory affairs.
- Negotiate and close complex, multi-year contracts with C-suite and senior decision-makers.
Cross-Functional Collaboration
- Collaborate closely with consultants, SMEs, and leadership across clinical, quality, supply chain, labeling, and M&A advisory services.
- Align business development activities with operational delivery to ensure client satisfaction and repeat engagements.
Required Qualifications
· Education: Advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or related field; PhD or MBA preferred. RAC or equivalent certification a plus.
· Experience:
- 10+ years in regulatory affairs, regulatory intelligence, or compliance within pharma/medical devices.
- 5+ years in consulting with direct client-facing and team leadership responsibilities.
- Proven track record of meeting or exceeding business development quotas and delivering measurable revenue growth.
· Regulatory Expertise: Mastery of global and Indian regulatory frameworks (FDA, EMA, CDSCO, WHO, ICH, GMP, GCP, QMS).
· Commercial Acumen: Skilled at identifying market opportunities, shaping client solutions, and closing strategic deals.
· Leadership: Demonstrated success in managing high-performance, multicultural teams.
· Communication: Exceptional English written and verbal skills with the ability to distill technical concepts for executive audiences.
Desired Traits
· Entrepreneurial, growth-oriented mindset with a balance of technical and commercial skills.
· Ability to operate seamlessly between strategic planning, operational oversight, and hands-on business development.
· High ethical standards and commitment to excellence in client delivery.
About Kamet Consulting Group
Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. We are an equal opportunity employer. All qualified applicants are encouraged to apply.
Why Join Us
- Contribute to meaningful technology in the life sciences domain.
- Work with a collaborative, forward-thinking team committed to innovation.
- Competitive compensation and benefits package.
- Flexible working arrangements and growth opportunities.
Director of Regulatory Research & Intelligence – India (Pharmaceutical & Medical Devices)
Posted 2 days ago
Job Viewed
Job Description
Job Title: Director of Regulatory Research & Intelligence
Location: Hybrid (Hyderabad)
Industry: Life Sciences / Healthcare Technology
Experience Level: 10+ years
Employment Type: Full-time
About the Role
Kamet Consulting Group is seeking a high-impact Director to lead our Global Regulatory Research & Intelligence function while driving strategic business development and market penetration. This dual-role leader will oversee a high-performing research intelligence team and own commercial growth initiatives, leveraging regulatory expertise to win new business, deepen client relationships, and expand our footprint in priority geographies.
The ideal candidate brings proven quota achievement over their tenure, deep knowledge of global regulatory frameworks, and the ability to translate regulatory insight into competitive advantage and revenue growth.
Core Responsibilities
· Regulatory Leadership & Intelligence Oversight
- Lead, mentor, and grow a multidisciplinary Regulatory Research & Intelligence team; set clear performance, quality, and delivery metrics.
- Define and evolve research agendas aligned to emerging regulatory trends (FDA, EMA, CDSCO, TGA, WHO, ICH, etc.) and client priorities.
- Oversee execution of complex regulatory intelligence projects—ensuring on-time, on-budget, and in-scope delivery.
- Serve as senior authority on regulatory intelligence, ensuring compliance with global quality standards and minimizing client risk.
- Present complex regulatory implications and recommendations to senior executives in clear, commercially relevant language.
Business Development & Market Penetration
- Develop and execute a go-to-market strategy to penetrate new regions and sectors within life sciences and healthcare technology.
- Leverage regulatory expertise to identify and secure high-value consulting, advisory, and outsourced service engagements.
- Own revenue targets and consistently achieve or exceed sales quotas through proactive pipeline building, solution selling, and account expansion.
- Partner with Leadership to position Kamet as a thought leader in global regulatory affairs.
- Negotiate and close complex, multi-year contracts with C-suite and senior decision-makers.
Cross-Functional Collaboration
- Collaborate closely with consultants, SMEs, and leadership across clinical, quality, supply chain, labeling, and M&A advisory services.
- Align business development activities with operational delivery to ensure client satisfaction and repeat engagements.
Required Qualifications
· Education: Advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or related field; PhD or MBA preferred. RAC or equivalent certification a plus.
· Experience:
- 10+ years in regulatory affairs, regulatory intelligence, or compliance within pharma/medical devices.
- 5+ years in consulting with direct client-facing and team leadership responsibilities.
- Proven track record of meeting or exceeding business development quotas and delivering measurable revenue growth.
· Regulatory Expertise: Mastery of global and Indian regulatory frameworks (FDA, EMA, CDSCO, WHO, ICH, GMP, GCP, QMS).
· Commercial Acumen: Skilled at identifying market opportunities, shaping client solutions, and closing strategic deals.
· Leadership: Demonstrated success in managing high-performance, multicultural teams.
· Communication: Exceptional English written and verbal skills with the ability to distill technical concepts for executive audiences.
Desired Traits
· Entrepreneurial, growth-oriented mindset with a balance of technical and commercial skills.
· Ability to operate seamlessly between strategic planning, operational oversight, and hands-on business development.
· High ethical standards and commitment to excellence in client delivery.
About Kamet Consulting Group
Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. We are an equal opportunity employer. All qualified applicants are encouraged to apply.
Why Join Us
- Contribute to meaningful technology in the life sciences domain.
- Work with a collaborative, forward-thinking team committed to innovation.
- Competitive compensation and benefits package.
- Flexible working arrangements and growth opportunities.
Director of Regulatory Research & Intelligence – India (Pharmaceutical & Medical Devices)
Posted today
Job Viewed
Job Description
Job Title: Director of Regulatory Research & Intelligence
Location: Hybrid (Hyderabad)
Industry: Life Sciences / Healthcare Technology
Experience Level: 10+ years
Employment Type: Full-time
About the Role
Kamet Consulting Group is seeking a high-impact Director to lead our Global Regulatory Research & Intelligence function while driving strategic business development and market penetration. This dual-role leader will oversee a high-performing research intelligence team and own commercial growth initiatives, leveraging regulatory expertise to win new business, deepen client relationships, and expand our footprint in priority geographies.
The ideal candidate brings proven quota achievement over their tenure, deep knowledge of global regulatory frameworks, and the ability to translate regulatory insight into competitive advantage and revenue growth.
Core Responsibilities
· Regulatory Leadership & Intelligence Oversight
- Lead, mentor, and grow a multidisciplinary Regulatory Research & Intelligence team; set clear performance, quality, and delivery metrics.
- Define and evolve research agendas aligned to emerging regulatory trends (FDA, EMA, CDSCO, TGA, WHO, ICH, etc.) and client priorities.
- Oversee execution of complex regulatory intelligence projects—ensuring on-time, on-budget, and in-scope delivery.
- Serve as senior authority on regulatory intelligence, ensuring compliance with global quality standards and minimizing client risk.
- Present complex regulatory implications and recommendations to senior executives in clear, commercially relevant language.
Business Development & Market Penetration
- Develop and execute a go-to-market strategy to penetrate new regions and sectors within life sciences and healthcare technology.
- Leverage regulatory expertise to identify and secure high-value consulting, advisory, and outsourced service engagements.
- Own revenue targets and consistently achieve or exceed sales quotas through proactive pipeline building, solution selling, and account expansion.
- Partner with Leadership to position Kamet as a thought leader in global regulatory affairs.
- Negotiate and close complex, multi-year contracts with C-suite and senior decision-makers.
Cross-Functional Collaboration
- Collaborate closely with consultants, SMEs, and leadership across clinical, quality, supply chain, labeling, and M&A advisory services.
- Align business development activities with operational delivery to ensure client satisfaction and repeat engagements.
Required Qualifications
· Education: Advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or related field; PhD or MBA preferred. RAC or equivalent certification a plus.
· Experience:
- 10+ years in regulatory affairs, regulatory intelligence, or compliance within pharma/medical devices.
- 5+ years in consulting with direct client-facing and team leadership responsibilities.
- Proven track record of meeting or exceeding business development quotas and delivering measurable revenue growth.
· Regulatory Expertise: Mastery of global and Indian regulatory frameworks (FDA, EMA, CDSCO, WHO, ICH, GMP, GCP, QMS).
· Commercial Acumen: Skilled at identifying market opportunities, shaping client solutions, and closing strategic deals.
· Leadership: Demonstrated success in managing high-performance, multicultural teams.
· Communication: Exceptional English written and verbal skills with the ability to distill technical concepts for executive audiences.
Desired Traits
· Entrepreneurial, growth-oriented mindset with a balance of technical and commercial skills.
· Ability to operate seamlessly between strategic planning, operational oversight, and hands-on business development.
· High ethical standards and commitment to excellence in client delivery.
About Kamet Consulting Group
Kamet Consulting Group is a Life Sciences Management Consulting firm providing Strategic Advisory, Implementation, Capability Building, and Outsourced Services to Pharmaceuticals, Medical Devices, Digital Health, and Consumer Health companies across their value chain. We are an equal opportunity employer. All qualified applicants are encouraged to apply.
Why Join Us
- Contribute to meaningful technology in the life sciences domain.
- Work with a collaborative, forward-thinking team committed to innovation.
- Competitive compensation and benefits package.
- Flexible working arrangements and growth opportunities.
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Jobs For Clinical Research Associate-Medical & Clinical Industry- Bangalore, Bengaluru, Karnataka...
Posted today
Job Viewed
Job Description
JOB DETAILS
1. Ensure thatclinical researchstudies are conducted in accordance with the protocol, standard operating procedures, goodclinicalpractice (GCP) guidelines, and other applicable regulatory requirements.
2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.
3. Review informed consent document / procedures.
4. Negotiate study budgets with potential investigators and assists with the execution of site contracts Provide monitoring visits and site management for a variety of protocols, sites
5. Administer protocol and other study-related training to assigned site personnel and establish regular lines of communication with the sites to manage ongoing project expectations and issues.
6. Evaluate the quality and integrity of the practices of the study site related to the proper conduct of the protocol and adherence to applicable regulations.
7. Escalate quality issues to the CPM / line manager, as deemed necessary.
8. Ensure accurate data reporting via review of site source documents and medical records.
9. Interpret data to identify protocol deviations and risks to subject safety/data integrity.
10. Perform investigational product accountability as per the protocol and Study Monitoring Plan.
FUNCTIONAL AREA
Research Associate, Clinical Research associate, Clinical Research associate Jobs in Bangalore, Clinical Research associate Jobs in Bengaluru, Clinical Research, Clinical Research Associate Jobs, Clinincal Research Associate Jobs in Tamil Nadu, Medical & Clinical Industry Jobs, Medical & Clinical Industry Jobs in Bangalore, Medical & Clinical Industry Jobs in Bengaluru, Jobs For Clinical Research Associate, Clinical Trial, Clinical Trial Analyst, Clinical Research Associate Jobs in Medical Industry, Medical & Clinical Recruitment Agencies in Bangalore, Medical & Clinical Placement Agencies in Bangalore, Medical & Clinical Placement Consultants in Bangalore, Medical & Clinical Recruitment Consultants in Bangalore, Medical Recruitment agencies in Bangalore, Medical & Clinical Industry Jobs Placement Agency in Bangalore, Medical & Clinical Recruitment Agencies in India, Medical & Clinical Placement Agencies in India, Medical & Clinical Placement Consultants in India, Medical & Clinical Recruitment Consultants in India, Medical Recruitment agencies in India, Medical & Clinical Industry Jobs Placement Agency in India.
Apply Now
Jobs For Clinical Research Associate- Medical & Clinical Industry- Chennai, Tamil Nadu-India- 4 L...
Posted today
Job Viewed
Job Description
JOB DETAILS
1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.
2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.
3. Review informed consent document / procedures.
4. Negotiate study budgets with potential investigators and assists with the execution of site contracts Provide monitoring visits and site management for a variety of protocols, sites
5. Administer protocol and other study-related training to assigned site personnel and establish regular lines of communication with the sites to manage ongoing project expectations and issues.
6. Evaluate the quality and integrity of the practices of the study site related to the proper conduct of the protocol and adherence to applicable regulations.
7. Escalate quality issues to the CPM / line manager, as deemed necessary.
8. Ensure accurate data reporting via review of site source documents and medical records.
9. Interpret data to identify protocol deviations and risks to subject safety/data integrity.
10. Perform investigational product accountability as per the protocol and Study Monitoring Plan.
FUNCTIONAL AREA
Research Associate, Clinical Research associate, Clinical Research associate Jobs in Chennai, Clinical Research associate Jobs in Tamil Nadu, Clinical Research, Clinical Research Associate Jobs, Clinincal Research Associate Jobs in Tamil Nadu, Medical & Clinical Industry Jobs, Medical & Clinical Industry Jobs in Chennai, Medical & Clinical Industry Jobs in tamil nadu, Jobs For Clinical Research Associate, Clinical Trial, Clinical Trial Analyst, Clinical Research Associate Jobs in Medical Industry, Medical & Clinical Recruitment Agencies in Chennai, Medical & Clinical Placement Agencies in Chennai, Medical & Clinical Placement Consultants in Chennai, Medical & Clinical Recruitment Consultants in Chennai, Medical Recruitment agencies in Chennai, Medical & Clinical Industry Jobs Placement Agency in Chennai, Medical & Clinical Recruitment Agencies in India, Medical & Clinical Placement Agencies in India, Medical & Clinical Placement Consultants in India, Medical & Clinical Recruitment Consultants in India, Medical Recruitment agencies in India, Medical & Clinical Industry Jobs Placement Agency in India.
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Clinical Research associate-Reputed Medical & Clinical Industry-Hyderabad, Telangana, India-5LPA-...
Posted today
Job Viewed
Job Description
JOB DETAILS
1) Creating and writing trial protocols, and presenting these to steering committee.
2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.
3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.
4) Liaise with ethics committee regarding rights, safety and well-being of trial subjects.
5) Ordering, tracking, and managing IP and trial materials.
6) Overseeing and documenting IP dispensing, inventory and reconciliation.
7) Protecting subjects’ confidentiality, updating their information, and verifying IP has been dispensed and administered according to protocol.
8) Conducting regular site visits, coordinating project meetings and writing visit reports.
FUNCTIONAL AREA
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