584 Senior Research Coordinator jobs in India
Clinical Research Coordinator
Bengaluru, Karnataka
ClinoGenesis Research Institute
Posted today
Job Viewed
Job Description
Clinical Research Coordinator (Freshers Only)
Location: (Insert City or "Across India" if remote/hybrid)
Organization: Clinogenesis Research Organization
Department: Clinical operations
Type: Full-Time
About the Role:
Clinogenesis Research Organization is offering an excellent opportunity for fresh graduates to launch their careers as Clinical Research Coordinators.
Please note: This position is strictly for freshers. Candidates with prior experience are not eligible for this role.
If youre passionate about clinical research and eager to grow in a structured, accredited environment, we invite you to apply.
Key Responsibilities:
- Assist with on-site coordination of clinical trial activities under supervision
- Maintain essential documents, site files, and case report forms
- Support the investigator in protocol compliance and patient coordination
- Ensure all trial activities adhere to ICH-GCP and ethical guidelines
- Participate in training sessions and team meetings as part of learning
Eligibility Criteria:
- Education: , B pharma , M pharma, B.Sc / M.Sc in Life Sciences, Pharmacy, Nursing, or equivalent healthcare field
- Experience: Freshers only
- Strong communication and organizational skills
- Eagerness to learn and grow in the clinical research domain
Why Start at Clinogenesis?
- Work alongside expert mentors and gain practical exposure
- Structured learning in a globally accredited research setup
- Continuous development and support for long-term career growth
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Coordinator
Pune, Maharashtra
SYS Research and Development
Posted today
Job Viewed
Job Description
Responsibilities for Clinical Research Coordinator
- Responsible for ensuring study is compliance with local and federal laws and regulations
- Recruits and screens potential study participants and performs intake assessments
- Creates and/or maintains all documents and records related to the study
- Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
- Manages the inventory of equipment and supplies related to the study and orders more as needed
- Attends meetings, events and seminars in order to promote the study
- Collects specimens and inputs data and patient information into electronic systems
- Creates reports on each study, including notes on protocols, workload, data collection, and more
Qualifications for Clinical Research Coordinator
- Excellent written and verbal communication skills
- Superior organizational and time management skills
- Capable of working independently with mínimal supervision and also as part of a team
- Skilled with standard computer programs including the MS Office suite
- Ability to speak a second language is an asset, but not required
- Understanding of medical terminology as well as standard clinical procedures and protocols
**Salary**: ₹10,086.00 - ₹39,784.68 per month
**Benefits**:
- Internet reimbursement
Schedule:
- Day shift
Supplemental Pay:
- Yearly bonus
- Responsible for ensuring study is compliance with local and federal laws and regulations
- Recruits and screens potential study participants and performs intake assessments
- Creates and/or maintains all documents and records related to the study
- Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
- Manages the inventory of equipment and supplies related to the study and orders more as needed
- Attends meetings, events and seminars in order to promote the study
- Collects specimens and inputs data and patient information into electronic systems
- Creates reports on each study, including notes on protocols, workload, data collection, and more
Qualifications for Clinical Research Coordinator
- Excellent written and verbal communication skills
- Superior organizational and time management skills
- Capable of working independently with mínimal supervision and also as part of a team
- Skilled with standard computer programs including the MS Office suite
- Ability to speak a second language is an asset, but not required
- Understanding of medical terminology as well as standard clinical procedures and protocols
**Salary**: ₹10,086.00 - ₹39,784.68 per month
**Benefits**:
- Internet reimbursement
Schedule:
- Day shift
Supplemental Pay:
- Yearly bonus
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Coordinator
Chennai, Tamil Nadu
SYS Research
Posted today
Job Viewed
Job Description
**Job description**
**Responsibilities for Clinical Research Coordinator**
- Responsible for ensuring study is compliance with local and federal laws and regulations
- Recruits and screens potential study participants and performs intake assessments
- Creates and/or maintains all documents and records related to the study
- Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
- Manages the inventory of equipment and supplies related to the study and orders more as needed
- Attends meetings, events and seminars in order to promote the study
- Collects specimens and inputs data and patient information into electronic systems
- Creates reports on each study, including notes on protocols, workload, data collection, and more
**Qualifications for Clinical Research Coordinator**
- Excellent written and verbal communication skills
- Superior organizational and time management skills
- Capable of working independently with mínimal supervision and also as part of a team
- Skilled with standard computer programs including the MS Office suite
- Ability to speak a second language is an asset, but not required
- Understanding of medical terminology as well as standard clinical procedures and protocols
**Salary**: ₹10,501.73 - ₹48,713.81 per month
**Benefits**:
- Internet reimbursement
Schedule:
- Day shift
Supplemental pay types:
- Performance bonus
Ability to commute/relocate:
- Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 1 year (preferred)
**Responsibilities for Clinical Research Coordinator**
- Responsible for ensuring study is compliance with local and federal laws and regulations
- Recruits and screens potential study participants and performs intake assessments
- Creates and/or maintains all documents and records related to the study
- Acts as a point of reference for study participants by answering questions and keeping them informed on the study progress
- Manages the inventory of equipment and supplies related to the study and orders more as needed
- Attends meetings, events and seminars in order to promote the study
- Collects specimens and inputs data and patient information into electronic systems
- Creates reports on each study, including notes on protocols, workload, data collection, and more
**Qualifications for Clinical Research Coordinator**
- Excellent written and verbal communication skills
- Superior organizational and time management skills
- Capable of working independently with mínimal supervision and also as part of a team
- Skilled with standard computer programs including the MS Office suite
- Ability to speak a second language is an asset, but not required
- Understanding of medical terminology as well as standard clinical procedures and protocols
**Salary**: ₹10,501.73 - ₹48,713.81 per month
**Benefits**:
- Internet reimbursement
Schedule:
- Day shift
Supplemental pay types:
- Performance bonus
Ability to commute/relocate:
- Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 1 year (preferred)
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Coordinator
Bitwise Solutions
Posted today
Job Viewed
Job Description
**Clinical Research Coordinator Duties and Responsibilities**
A Clinical Research Coordinator is responsible for a variety of duties including the following:
- Overseeing the trouble-free running of clinical trials
- Collecting data obtained from research, coding and analyzing it
- Managing budgets set aside for research
- Communicating with participants regarding study objectives
- Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules
- Liaising with laboratories regarding research findings
- Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards
- Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines
- Directing the collection, labeling, storage and transport of all specimens
- Making sure that all equipment and supplies needed for the study are in-stock and in good working order
Build a Job Description
**Salary**: ₹15,000.00 - ₹38,000.00 per month
**Benefits**:
- Internet reimbursement
Schedule:
- Day shift
Supplemental pay types:
- Performance bonus
Ability to commute/relocate:
- Sagarpata, Orissa: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Higher Secondary(12th Pass) (preferred)
**Experience**:
- total work: 1 year (preferred)
A Clinical Research Coordinator is responsible for a variety of duties including the following:
- Overseeing the trouble-free running of clinical trials
- Collecting data obtained from research, coding and analyzing it
- Managing budgets set aside for research
- Communicating with participants regarding study objectives
- Administering questionnaires and monitoring participants to ensure they adhere to the study’s rules
- Liaising with laboratories regarding research findings
- Monitoring the study to ensure that it complies with protocols, is ethically-conducted and follows regulatory standards
- Maintaining research records of study activity, including case report forms, drug dispensation records or other regulatory forms as per FDA guidelines
- Directing the collection, labeling, storage and transport of all specimens
- Making sure that all equipment and supplies needed for the study are in-stock and in good working order
Build a Job Description
**Salary**: ₹15,000.00 - ₹38,000.00 per month
**Benefits**:
- Internet reimbursement
Schedule:
- Day shift
Supplemental pay types:
- Performance bonus
Ability to commute/relocate:
- Sagarpata, Orissa: Reliably commute or planning to relocate before starting work (required)
**Education**:
- Higher Secondary(12th Pass) (preferred)
**Experience**:
- total work: 1 year (preferred)
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Coordinator
Surat, Gujarat
Concept Clinical Services
Posted today
Job Viewed
Job Description
Bsc/Msc life science/paramedical
- B.Pharm/M. Pharm/ Pharm. D
- Freshers or Experienced
- Willing to build a career in the filed of research with good exposure and new development in terms of technologies and treatment.
- Working place will be the hospital.
- Good communication skill with basic computer skill.
- should be a good learner with adaptable, Soft skills and sincere.
**Job Types**: Full-time, Regular / Permanent, Fresher, Internship
Contract length: 24 months
**Salary**: ₹7,500.00 - ₹12,000.00 per month
**Benefits**:
- Flexible schedule
Schedule:
- Day shift
- Flexible shift
Application Question(s):
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 1 year (preferred)
- B.Pharm/M. Pharm/ Pharm. D
- Freshers or Experienced
- Willing to build a career in the filed of research with good exposure and new development in terms of technologies and treatment.
- Working place will be the hospital.
- Good communication skill with basic computer skill.
- should be a good learner with adaptable, Soft skills and sincere.
**Job Types**: Full-time, Regular / Permanent, Fresher, Internship
Contract length: 24 months
**Salary**: ₹7,500.00 - ₹12,000.00 per month
**Benefits**:
- Flexible schedule
Schedule:
- Day shift
- Flexible shift
Application Question(s):
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 1 year (preferred)
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Coordinator
Ahmedabad, Gujarat
Apollo Research and innovations
Posted today
Job Viewed
Job Description
Position - Clinical Research Coordinator
Experience - Above 1 Years
Timing - General Shift
Qualification - Life Science
Salary - CTC2.20 L per annum (based on your experience it may differ)
Contract Period - Minimum 2 Years(No Bond)
Location - Ahmedabad
preferred - Male (only)
Language Knows - Guajarati (Must), Hindi & English
Contact Number - 044-28295465
JOB Description Clinical Research Coordinator
- To have the good knowledge of regulatory and GCP guidelines.
- Ability to communicate properly between the physician, patient & the site head.
- Assist Senior CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures.
- Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents.
- Present in Site Initiation Visit, Monitoring Visits, Site Closeout Visit.
- CRF, e-CRF entry, Data Query resolution.
- Coordinate between the local/Central laboratory and courier for the shipment.
- Assist the pharmacist in drug accountability and temperature maintaining logs.
- Assist the Sr. CRC in maintaining the accountability of study materials and in scheduling study procedures.
- Endow the required file notes, weekly and monthly and monthly report to the reporting authority.
- Tracking the status of all study activities.
- Report Site head daily and take advice for further action.
**Salary**: ₹10,000.00 - ₹15,000.00 per month
Schedule:
- Day shift
Ability to commute/relocate:
- Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (required)
**Experience**:
- total work: 4 years (preferred)
Experience - Above 1 Years
Timing - General Shift
Qualification - Life Science
Salary - CTC2.20 L per annum (based on your experience it may differ)
Contract Period - Minimum 2 Years(No Bond)
Location - Ahmedabad
preferred - Male (only)
Language Knows - Guajarati (Must), Hindi & English
Contact Number - 044-28295465
JOB Description Clinical Research Coordinator
- To have the good knowledge of regulatory and GCP guidelines.
- Ability to communicate properly between the physician, patient & the site head.
- Assist Senior CRC in Screening including informed consent process, randomization, enrolment & follow-up (including Telephonic Follow-up) process & procedures.
- Maintenance of Investigator Master File as per Good documentation practices & SOP including generation of source documents.
- Present in Site Initiation Visit, Monitoring Visits, Site Closeout Visit.
- CRF, e-CRF entry, Data Query resolution.
- Coordinate between the local/Central laboratory and courier for the shipment.
- Assist the pharmacist in drug accountability and temperature maintaining logs.
- Assist the Sr. CRC in maintaining the accountability of study materials and in scheduling study procedures.
- Endow the required file notes, weekly and monthly and monthly report to the reporting authority.
- Tracking the status of all study activities.
- Report Site head daily and take advice for further action.
**Salary**: ₹10,000.00 - ₹15,000.00 per month
Schedule:
- Day shift
Ability to commute/relocate:
- Chennai, Tamil Nadu: Reliably commute or planning to relocate before starting work (required)
**Experience**:
- total work: 4 years (preferred)
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Coordinator
Bengaluru, Karnataka
Clini launch Research Institute
Posted today
Job Viewed
Job Description
**Job Summary**:
**Responsibilities**:
**Protocol Development**:
Collaborate in the development of clinical trial protocols, ensuring alignment with regulatory requirements and study objectives.
Provide input into the design of study documents, such as Case Report Forms (CRFs) and Informed Consent Forms (ICFs).
**Site Selection and Monitoring**:
Conduct pre-study site evaluations and initiate investigator sites.
Monitor clinical sites to ensure protocol adherence, data accuracy, and regulatory compliance.
Provide training and support to site staff as needed.
**Regulatory Compliance**:
Ensure compliance with applicable regulatory standards, ICH-GCP guidelines, and company SOPs.
Assist in preparing and submitting regulatory documents for ethics committee and regulatory authority approval.
**Data Management**:Oversee data collection, review, and resolution of discrepancies.
Ensure the completeness, accuracy, and quality of clinical trial data.
**Safety Reporting**:
Manage and report serious adverse events (SAEs) in compliance with regulatory requirements.
Collaborate with the Safety Department to ensure timely reporting and resolution of safety issues.
**Study Close-Out**:
Coordinate and conduct site close-out activities.
Ensure proper archiving of study documents in accordance with regulatory standards.
**Qualifications**:
- Bachelor's or higher degree in life sciences or a related field.
- Previous experience as a Clinical Research Associate or in a similar role.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent organizational and communication skills.
- Ability to work independently and collaboratively in a team environment.
- Proficiency in Microsoft Office and familiarity with electronic data capture systems.
**Certifications**:Relevant certifications (e.g., SoCRA, ACRP) are a plus.
**Job Types**: Full-time, Permanent, Fresher
**Salary**: Up to ₹30,363.97 per month
**Benefits**:
- Health insurance
- Provident Fund
Schedule:
- Day shift
- Morning shift
Supplemental pay types:
- Performance bonus
- Yearly bonus
**Experience**:
- total work: 1 year (preferred)
Ability to Commute:
- Bangalore, Karnataka (required)
Ability to Relocate:
- Bangalore, Karnataka: Relocate before starting work (required)
**Speak with the employer**
+91
**Responsibilities**:
**Protocol Development**:
Collaborate in the development of clinical trial protocols, ensuring alignment with regulatory requirements and study objectives.
Provide input into the design of study documents, such as Case Report Forms (CRFs) and Informed Consent Forms (ICFs).
**Site Selection and Monitoring**:
Conduct pre-study site evaluations and initiate investigator sites.
Monitor clinical sites to ensure protocol adherence, data accuracy, and regulatory compliance.
Provide training and support to site staff as needed.
**Regulatory Compliance**:
Ensure compliance with applicable regulatory standards, ICH-GCP guidelines, and company SOPs.
Assist in preparing and submitting regulatory documents for ethics committee and regulatory authority approval.
**Data Management**:Oversee data collection, review, and resolution of discrepancies.
Ensure the completeness, accuracy, and quality of clinical trial data.
**Safety Reporting**:
Manage and report serious adverse events (SAEs) in compliance with regulatory requirements.
Collaborate with the Safety Department to ensure timely reporting and resolution of safety issues.
**Study Close-Out**:
Coordinate and conduct site close-out activities.
Ensure proper archiving of study documents in accordance with regulatory standards.
**Qualifications**:
- Bachelor's or higher degree in life sciences or a related field.
- Previous experience as a Clinical Research Associate or in a similar role.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent organizational and communication skills.
- Ability to work independently and collaboratively in a team environment.
- Proficiency in Microsoft Office and familiarity with electronic data capture systems.
**Certifications**:Relevant certifications (e.g., SoCRA, ACRP) are a plus.
**Job Types**: Full-time, Permanent, Fresher
**Salary**: Up to ₹30,363.97 per month
**Benefits**:
- Health insurance
- Provident Fund
Schedule:
- Day shift
- Morning shift
Supplemental pay types:
- Performance bonus
- Yearly bonus
**Experience**:
- total work: 1 year (preferred)
Ability to Commute:
- Bangalore, Karnataka (required)
Ability to Relocate:
- Bangalore, Karnataka: Relocate before starting work (required)
**Speak with the employer**
+91
This advertiser has chosen not to accept applicants from your region.
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6
Clinical Research Coordinator
Surat, Gujarat
Concept Clinical Services
Posted today
Job Viewed
Job Description
Msc life sciences
- B.Pharm/M. Pharm/ Pharm. D
- Freshers or Experienced
- Willing to build a career in the filed of Clinical Research with good exposure and new development in terms of technologies and treatment.
- Working place will be the multispecialtiy hospital in surat
- Good communication skill with basic computer skill.
- should be a good learner with adaptable, Soft skills and sincere.
**Job Types**: Full-time, Permanent, Fresher
**Benefits**:
- Flexible schedule
Schedule:
- Day shift
Supplemental Pay:
- Yearly bonus
Application Question(s):
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 1 year (preferred)
Application Deadline: 05/08/2024
- B.Pharm/M. Pharm/ Pharm. D
- Freshers or Experienced
- Willing to build a career in the filed of Clinical Research with good exposure and new development in terms of technologies and treatment.
- Working place will be the multispecialtiy hospital in surat
- Good communication skill with basic computer skill.
- should be a good learner with adaptable, Soft skills and sincere.
**Job Types**: Full-time, Permanent, Fresher
**Benefits**:
- Flexible schedule
Schedule:
- Day shift
Supplemental Pay:
- Yearly bonus
Application Question(s):
**Education**:
- Bachelor's (preferred)
**Experience**:
- total work: 1 year (preferred)
Application Deadline: 05/08/2024
This advertiser has chosen not to accept applicants from your region.
7