CrawlJobs Logo

Clinical Data Coordinator II

India, Bengaluru · Job Posted February 16, 2026
Apply Position
Job Link Share

Job Description

At Quanticate, we're pioneers in providing top-tier statistical and data management support to our clients. Are you passionate about clinical research and data excellence? Do you thrive in fast-paced, dynamic environments where your attention to detail can make a real impact on patient outcomes? We’re looking for a Clinical Data Coordinator II to be at the heart of our studies, ensuring top-quality data from start to finish.

Job Responsibility

  • Support end-to-end Clinical Data Management activities across multiple studies
  • Assist with database testing and validation prior to study activation
  • Prepare and maintain study-specific Data Management documentation
  • Review CRFs critically, identifying data inconsistencies, errors, or missing information
  • Raise, track, and resolve data queries and Data Clarification Forms (DCFs)
  • Manage self-evident queries and allowable data changes within the database
  • Perform quality control checks on data entry and database outputs
  • Support study close-out activities, including preparation of archival documentation
  • Ensure compliance with SOPs, ICH-GCP, regulatory requirements, and client standards
  • Contribute to process improvement initiatives and data management best practices
  • Perform medical coding activities when assigned
  • Collaborate with offshore data processing and programming teams
  • Provide project updates and support progress tracking using reports and metrics
  • Take on ad-hoc tasks as required to support project and team objectives

Requirements

  • Strong understanding of Clinical Data Management processes
  • Solid knowledge of ICH-GCP guidelines and regulatory requirements related to data handling
  • Familiarity with CRO and sponsor-driven study standards
  • Prior experience in Clinical Data Management or a similar role
  • Hands-on experience with at least one CDM system (e.g., Oracle Clinical, Medidata Rave, Inform)
  • Experience supporting multiple studies or managing competing priorities is preferred
  • Excellent attention to detail and strong analytical thinking
  • Good written and verbal communication skills
  • Strong organizational and time-management abilities
  • Ability to work effectively in a fast-changing, deadline-driven environment
  • Comfortable working with offshore or remote teams
  • Proficient in Microsoft Word and Excel
  • Team-oriented mindset with the ability to motivate and collaborate effectively

What we offer

  • Competitive salary
  • Flexible working hours
  • Holidays (Annual Leave, Sick Leave, Casual Leave and Bank holidays)
  • Medical Insurance for self and immediate family
  • Gratuity
  • Accidental Coverage
  • Quanticate offers a variety of different learning development opportunities to help you progress (mentoring, coaching, e- learning, job shadowing)

Looking for more opportunities?

Search for other job offers that match your skills and interests.

Similar Jobs for

Clinical Data Coordinator II

8 matching positions

Data Coordinator II

Labcorp is seeking a Data Coordinator II to join our team Data Reconciliation Ce...
Location
Location
India , Bengaluru
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Science
  • 4 years experience working in a clinical trial environment or in a relevant industry within a regulated environment
  • Master's degree in Science
  • Any background of medical lab technician or awareness and functioning of a laboratory is preferrable
  • Have an excellent attention to detail
  • Flexibility to work overtime as needed
  • Ability to work independently or in a team environment
  • Comfortable working under minimal supervision
Job Responsibility
Job Responsibility
  • Individual Contributor role performing highly complex revisions to data within CLS database - Zavacor per defined data revision processes, including review of requests, and performing self-quality checks
  • Attend required training to maintain role competencies and support continuous development
  • participate in Labcorp Corporate training, attend mandatory DRC meetings, and participate in ongoing training initiatives regarding process and system changes or updates related to data revisions
  • Resolve database and project issues, escalating to DRC management or other Labcorp departments as needed for full resolution
  • QC, coach and mentor New Hires & others as needed
  • Ensure compliance with departmental guidelines and company standards through adherence to SOPs, WIs, management communications, and other pertinent documentation
  • Revision tasks would involve performing repetitive work and need sitting in front of a terminal for many hours during the working day
  • Fulltime
Read More
Arrow Right

Clinical Research Coordinator II

Must be comfortable with 50% travel. Highly prefer someone who lives in the Nort...
Location
Location
United States
Salary
Salary:
Not provided
freseniuskidneycare.com Logo
Fresenius Kidney Care Eupora
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • 2 to 4 years of clinical research experience, or has successfully performed in the role of Clinical Research Coordinator I for a minimum of 3 years and demonstrated outstanding performance through performance evaluations, certification and other job performance measures
  • Critical care, nephrology and/ or cardiac experience desirable
  • Willing to pursue CCRC or CCRP certification when eligible
  • Current state licensure, if applicable
  • Good computer skills: Microsoft Office minimally
  • Excellent communication and organizational skills
  • Ability to work independently, and exhibit diplomacy and problem solving skills in the performance of this role
Job Responsibility
Job Responsibility
  • Assists with the determination of the guidelines for the collection of clinical data and coordinates and implements procedures and processes for data collection
  • Coordinates all aspects of study subject care from pre-screening through study completion as defined by the protocol and Principal Investigator (PI) delegation
  • Protect the rights and the well-being of subjects enrolled in studies
  • Ensures thorough, individualized, protocol-based study subject education on all study process requirements including but not limited to: informed consent, study participation obligations, appropriate use of investigational product, safety, privacy, rights and responsibilities
  • Develops processes for methodically monitoring the status of study subjects as they progress through the study’s timeline of activities
  • Regularly evaluates the study subjects’ condition and communicates/documents concerns to PI to ensure subject safety
  • Accurately documents study subject activities as outlined by the protocol
  • Maintains documents according to applicable HIPAA and regulatory requirements
  • Implements study-specific quality goals and practices
  • Acts as the point of contact or lead person in a facility/practice to oversee protocol compliance
Read More
Arrow Right

Clinical Research Coordinator II - Precision Medicine

A Clinical Research Coordinator II (CRC II) position is available for the Precis...
Location
Location
United States , BOSTON
Salary
Salary:
56000.00 - 63700.00 USD / Year
dana-farber.org Logo
Dana-Farber Cancer Institute
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • bachelor's degree or 2 years of experience as a Dana-Farber Clinical Research Coordinator
  • 1-3 years of relevant experience
  • preference for those with a background in medical or scientific research or a technology-oriented business environment
  • excellent organization and communications skills
  • strong interpersonal skills
  • detail oriented
  • ability to effectively manage time and prioritize workload
  • must practice discretion and adhere to hospital confidentiality guidelines
  • computer skills including the use of Microsoft Office
Job Responsibility
Job Responsibility
  • liaise between the LSP, DF/HCC hospitals, and external investigators to facilitate highly collaborative translational biomarker driven research
  • facilitate the emerging fields of cancer spatial biology
  • work closely with principal investigators, program managers, biomarker researchers, and data scientists
  • primary data collection and management of patient clinical information as it pertains to participation in clinical trials and patient consent
  • ensure timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities
  • support and maintain participant/subject trial binders and maintain regulatory binders
  • ensure study compliance with all state, federal, and IRB requirements
  • screen patients for protocol eligibility
  • obtain informed consent for non-treatment trials
  • register study participants with the clinical trials management system, ONCORE
  • Fulltime
Read More
Arrow Right

Clinical Research Coordinator II

This role requires 100% travel. PURPOSE AND SCOPE: Works under the supervision o...
Location
Location
United States , Las Vegas
Salary
Salary:
Not provided
freseniuskidneycare.com Logo
Fresenius Kidney Care Eupora
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's Degree or an equivalent combination of education and experience
  • Graduate of a technical program in healthcare (e.g. LVN/LPN, Medical Assistant or Dialysis Technician) AA in Life Sciences or other health related field
  • 2 to 5 years' healthcare experience with Dialysis experience preferred
  • Research experience preferred
  • Willing to pursue CCRC or SoCRA certification when eligible
  • Current appropriate state licensure if applicable
  • Proficient with PCs and Microsoft Office applications
  • Good communication and organizational skills
  • Ability to work independently
Job Responsibility
Job Responsibility
  • Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to in accordance with FDA, GCP, and ICH Guidelines
  • Under the supervision of the Principal Investigator (PI) and appropriate management prepares and submits regulatory documents in an accurate and timely manner
  • In collaboration with the PI, incorporates clinical judgment and knowledge of protocol to identify potential study participants according to inclusion and exclusion criteria
  • Obtains informed consent according to GCP
  • Schedules subject visits
  • Prepares labs/tests per protocol
  • Responsible for study drug storage and drug accountability according to the parameters of the study protocol and sponsor requirements
  • Administers the investigational product according to the parameters of the study protocol and under the direction of the physician
  • Monitors and evaluates patients' condition with regard to the investigational product
  • Consults with PI regarding the appropriate administration of investigational product
What we offer
What we offer
  • Healthcare
  • Continuing Education
  • Paid Time Off
  • Collaborative Environment
  • Additional Perks
  • 401(k) Retirement Saving
  • Fulltime
Read More
Arrow Right

Clinical Studies Coordinator II, Translational Neuroscience

Under departmental direction, coordinates activities to support multiple researc...
Location
Location
United States , Winston Salem
Salary
Salary:
26.55 - 39.85 USD / Hour
advocatehealth.com Logo
Advocate Health Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree with two years experience in clinical research
  • or an equivalent combination of experience and education
  • SOCRA or ACRP Certification preferred
  • Must complete the CITI certification for Human Subject Research if not already completed
  • All additional required WakeOne training for research coordinators
  • Excellent interpersonal, oral, and written communication skills
  • Excellent reading comprehension
  • Strong organizational skills
  • EPIC/WakeOne proficiency to include appropriate documentation of research notes
  • Proficient in the use of OnCore/WISER Clinical Trial Management System
Job Responsibility
Job Responsibility
  • Coordinates activities to support multiple research studies of all phases
  • Serves as the principal administrative liaison for assigned studies
  • Develops and maintains recordkeeping systems and procedures to ensure compliance
  • Attends clinic as needed to perform activities including recruitment, administering questionnaires
  • Responsible for the compilation, registration and submission of data
  • Works under the direction of the Study Investigators or Clinical Research Nurse Manager
  • Plays an active role in recruitment of patients to study
  • Performs protocol specific duties required per the research protocol
  • Obtains or assists the Principal Investigator in obtaining informed consent
  • Fulfills sponsor requirements related to reportable information including adverse events
What we offer
What we offer
  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
  • Opportunity for annual increases based on performance
  • Premium pay such as shift, on call, and more
  • Incentive pay for select positions
  • Fulltime
Read More
Arrow Right

Clinical Studies Coordinator II, Translational Neuroscience

Under departmental direction, coordinates activities to support multiple researc...
Location
Location
United States , Winston Salem
Salary
Salary:
26.55 - 39.85 USD / Hour
advocatehealth.com Logo
Advocate Health Care
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree with two years experience in clinical research
  • or an equivalent combination of experience and education
  • SOCRA or ACRP Certification preferred
  • Must complete the CITI certification for Human Subject Research if not already completed
  • All additional required WakeOne training for research coordinators
  • Excellent interpersonal, oral, and written communication skills
  • Excellent reading comprehension
  • Strong organizational skills
  • EPIC/WakeOne proficiency to include appropriate documentation of research notes
  • Proficient in the use of OnCore/WISER Clinical Trial Management System
Job Responsibility
Job Responsibility
  • Coordinates activities to support multiple research studies of all phases
  • Serves as the principal administrative liaison for assigned studies
  • Develops and maintains recordkeeping systems and procedures to ensure compliance
  • Attends clinic as needed to perform activities including recruitment, administering questionnaires
  • Responsible for the compilation, registration and submission of data
  • Works under the direction of the Study Investigators or Clinical Research Nurse Manager
  • Plays an active role in recruitment of patients to study
  • Performs protocol specific duties required per the research protocol
  • Obtains or assists the Principal Investigator in obtaining informed consent
  • Fulfills sponsor requirements related to reportable information including adverse events
What we offer
What we offer
  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
  • Opportunity for annual increases based on performance
  • Premium pay such as shift, on call, and more
  • Incentive pay for select positions
  • Fulltime
Read More
Arrow Right

Clinical Research Coordinator II

We are seeking a motivated and experienced Clinical Research Coordinator II to s...
Location
Location
United States , Nashua
Salary
Salary:
60000.00 - 75000.00 USD / Year
solomonpage.com Logo
Solomon Page
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 3 years of direct patient-facing clinical research experience in industry-sponsored, interventional drug trials
  • Ophthalmology experience (Technician or Ophthalmology CRC background)
  • Strong patient communication skills with the ability to build trust and support retention
  • Experience with patient care, recruitment, lab specimen handling, monitoring, and audits
  • Excellent organizational, multitasking, and time management skills
  • Willingness and ability to travel regularly (up to 50%) and on site when not traveling
Job Responsibility
Job Responsibility
  • Coordinate day-to-day clinical trial activities across multiple therapeutic areas, including ophthalmology, dermatology, and pulmonology
  • Support studies at headquarters and satellite site locations
  • Conduct patient-facing activities, including informed consent, visit scheduling, and follow-up
  • Manage patient recruitment and enrollment through database reviews, outreach, pre-screening, and ongoing communication
  • Perform blood draws and manage biospecimen processing and shipping per protocol
  • Maintain accurate study documentation, source data, and regulatory binders across CTMS, EDC, and other systems
  • Support monitoring visits and participate in internal and external audits
  • Serve as a key liaison between sponsors, CROs, investigators, and internal teams
  • Provide cross-functional support as needed to meet study timelines and goals
What we offer
What we offer
  • medical
  • dental
  • 401(k)
  • direct deposit
  • commuter benefits
  • Fulltime
Read More
Arrow Right

Clinical Research Coordinator II

We are seeking a motivated and experienced Clinical Research Coordinator II to s...
Location
Location
United States , Nashua
Salary
Salary:
60000.00 - 75000.00 USD / Year
solomonpage.com Logo
Solomon Page
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Minimum of 3 years of direct patient-facing clinical research experience in industry-sponsored, interventional drug trials
  • Ophthalmology experience (Technician or Ophthalmology CRC background)
  • Strong patient communication skills with the ability to build trust and support retention
  • Experience with patient care, recruitment, lab specimen handling, monitoring, and audits
  • Excellent organizational, multitasking, and time management skills
  • Willingness and ability to travel regularly (up to 50%)
Job Responsibility
Job Responsibility
  • Coordinate day-to-day clinical trial activities across multiple therapeutic areas, including ophthalmology, dermatology, and pulmonology
  • Support studies at headquarters and satellite site locations
  • Conduct patient-facing activities, including informed consent, visit scheduling, and follow-up
  • Manage patient recruitment and enrollment through database reviews, outreach, pre-screening, and ongoing communication
  • Perform blood draws and manage biospecimen processing and shipping per protocol
  • Maintain accurate study documentation, source data, and regulatory binders across CTMS, EDC, and other systems
  • Support monitoring visits and participate in internal and external audits
  • Serve as a key liaison between sponsors, CROs, investigators, and internal teams
  • Provide cross-functional support as needed to meet study timelines and goals
What we offer
What we offer
  • medical
  • dental
  • 401(k)
  • direct deposit
  • commuter benefits
  • Fulltime
Read More
Arrow Right