Indero Hiring – Clinical Data Coordinator | Clinical Data Management | India
Indero is hiring a Clinical Data Coordinator for its CRO – Biometrics team in India.
This entry-level position supports clinical data management activities, including data review, reconciliation, discrepancy management, and study reporting.
Candidates with a B.Sc. or related qualification can apply, while clinical data management experience and EDC system knowledge are considered assets.
The role is a permanent, full-time position for candidates who can legally work in India.
Company Overview
Indero is a contract research organization (CRO) specializing in dermatology and rheumatology. The organization has operated since 2000 and provides clinical research and related services across North America and Europe.
Indero’s stated values include collaboration, innovation, reliability, and responsiveness.
Job Details
Clinical Data Coordinator – India
- Company: Indero
- Department: CRO – Biometrics
- Location: India
- Job Type: Permanent, Full-Time
- Experience Level: Entry-Level
- Work Eligibility: Applicants must be legally authorized to work in India
Clinical Data Management Responsibilities
Data Review & Reconciliation
The Clinical Data Coordinator will support the project team, sponsors, and external vendors with clinical data management activities, including:
- Providing general data management support to project teams, sponsors, and external vendors.
- Supporting the Lead Data Manager with data review.
- Supporting data reconciliation activities.
- Supporting discrepancy management.
- Monitoring study status, including enrollment and CRFs monitored or approved.
- Maintaining study metrics and providing data status reports to the project team as required.
- Generating ad-hoc study reports.
Clinical Database & Study Documentation
- Supporting user maintenance.
- Assisting with User Acceptance Testing (UAT).
- Assisting with clinical database design.
- Assisting with creation of the Data Management Plan (DMP) and other clinical data management documentation.
- Assisting in ensuring that data management documentation is complete and up to date in the Trial Master File (TMF).
Ideal Profile
Education
- B.Sc. or related field
Experience
- 1 year of clinical data management experience in the pharmaceutical industry or a CRO environment is considered an asset.
- Experience using an EDC system, such as Medidata Rave or Medrio, is considered an important asset.
Knowledge & Skills
- Skilled in computer technology with the ability to learn new applications.
- General knowledge of CDASH/SDTM is considered an asset.
- Highly organized and detail-oriented.
- Effective project planning and time management skills.
- Strong verbal and written communication skills in English.
- French language skills are considered an asset.
- Ability to work in a fast-paced environment and prioritize multiple competing demands.
- Strong interpersonal, communication, problem-solving, and organizational skills.
- Ability to work independently as well as in a team environment.
- Understanding of the drug development process and applicable regulations.
- Knowledge of Good Clinical Practices (GCP) and ICH Guidelines.
- Understanding of applicable Health Canada and FDA regulations/guidelines.
Why This Role May Suit You
According to the source, this position is suitable for candidates who:
- Have strong analytical abilities and are comfortable working with data.
- Enjoy working with systems and technology.
- Are interested in continuously learning.
- Prefer working in a collaborative team environment where ideas are heard and valued.
Work Environment & Benefits
The source states that employees in this position are eligible for:
- Flexible work schedule
- Permanent full-time employment
- Company benefits package
- Ongoing learning and development
Eligible Qualification Courses
B.Sc. | Related Science Degree
The source specifically mentions B.Sc. or a related field. It does not provide a detailed list of individual B.Sc. specializations.
How to Apply
Interested and eligible candidates can apply through the official application page provided for this position:
Apply for Clinical Data Coordinator – India
Important: Indero only accepts applicants who can legally work in India.
Job Summary
| Category | Details |
|---|---|
| Company | Indero |
| Vacancies | Clinical Data Coordinator |
| Required Education | B.Sc. or related field |
| Experience | Entry-level; 1 year clinical data management experience in pharmaceutical or CRO environment is an asset |