Phastar is hiring a Clinical Data Coordinator for a remote position in India. The role is suitable for professionals with 2–5 years of experience in clinical data management, clinical trials, CRO, pharmaceutical, or academic research environments.

The position focuses on clinical data quality, study protocol review, SAS and Excel-based data review, Medidata Rave database testing, SAE reconciliation, coded data listings, third-party data reconciliation, and collaboration with CROs and internal stakeholders.

Candidates with experience in Clinical Data Management (CDM), Medidata Rave, SAS listings, CDISC standards, clinical trial databases, data reconciliation, and edit-check review may find this opportunity particularly relevant.

Phastar Clinical Data Coordinator Job Details

Phastar’s current India data-management opportunities also include remote clinical data coordination work involving data quality checks, listings review, coded data and clinical database activities.

What Does a Clinical Data Coordinator Do at Phastar?

The Clinical Data Coordinator supports the delivery of high-quality clinical trial data throughout the study lifecycle.

The role involves working with CROs, internal stakeholders, Programme Managers, and study teams to review clinical data, identify discrepancies, support reconciliation activities, and ensure that clinical databases and associated documentation meet study requirements.

Phastar’s clinical data work includes activities such as eCRF and edit-check testing, data-listing review, query management, clinical coding, third-party data management, and database quality activities.

Key Responsibilities

As a Clinical Data Coordinator, the selected candidate may be responsible for:

• Building strong working relationships with CROs and internal stakeholders.
• Reviewing clinical study protocols and providing data-management recommendations.
• Supporting the Programme Manager and collaborating with study and support teams.
• Applying clinical data management principles throughout study delivery.
• Reviewing clinical data using SAS listings and Microsoft Excel.
• Performing or supporting SAE reconciliation.
• Reviewing coded clinical data listings.
• Conducting database testing within Medidata Rave.
• Reviewing Medidata Rave edit-check outputs and taking appropriate action.
• Reviewing documentation associated with third-party data.
• Updating study documents and reviewing reconciliation outputs.
• Preparing clinical data management status reports.
• Supporting data quality and study-level reconciliation activities.
• Working within clinical trial environments involving CRO, pharmaceutical, or academic research teams.

Eligibility for Phastar Clinical Data Coordinator

The advertised position specifies 2–5 years of professional experience and emphasizes practical clinical data management expertise.

Educational Qualification

The job listing categorizes the educational requirement as Any Graduate. Therefore, the posting does not restrict applicants to one specific bachelor’s or master’s degree.

Relevant academic backgrounds may include:

• B.Pharm / M.Pharm
• Pharm.D
• B.Sc / M.Sc
• Life Sciences
• Biotechnology
• Biochemistry
• Microbiology
• Nursing or allied healthcare fields
• Other relevant graduate qualifications

However, degree alone is not enough for this position. The strongest candidates are those who can demonstrate hands-on experience in clinical trials and clinical data management.

Experience and Technical Skills Required

Candidates should ideally have experience in the following areas:

SAS Listings and Excel

The position requires the ability to review clinical data using SAS listings and Excel, including SAE reconciliations and coded-data listings.

Medidata Rave

Experience with Medidata Rave database testing is an important requirement. Candidates should be comfortable reviewing edit-check outputs and taking appropriate action based on findings.

CDISC Standards

Familiarity with CDISC standards is specifically mentioned in the requirements. Knowledge of clinical data standards can therefore strengthen an applicant’s profile.

Clinical Trials

Applicants should have experience working in a clinical trials environment, such as a CRO, pharmaceutical company, biotechnology organization, or academic research setting.

Third-Party Data

Experience reviewing third-party data documentation, updating documents, and reviewing reconciliation outputs is also relevant.

Additional EDC Platforms

Experience with Medrio, Viedoc, or CrsCube is considered advantageous.

Skills That Can Strengthen Your Application

Candidates targeting this Clinical Data Coordinator job should highlight experience with:

• Clinical Data Management
• Clinical Trial Data
• Medidata Rave
• Electronic Data Capture (EDC)
• SAS
• Microsoft Excel
• CDISC
• SAE Reconciliation
• Data Reconciliation
• Edit Checks
• Query Management
• Clinical Coding
• Data Listings
• Third-Party Data
• Protocol Review
• Clinical Database Testing
• Study Documentation
• CRO Operations
• Data Quality Management

Salary for Phastar Clinical Data Coordinator

Phastar has not disclosed the salary for this vacancy in the supplied job listing.

For informational purposes only, a reasonable India market estimate for a specialized Clinical Data Coordinator with 2–5 years of relevant experience could be approximately ₹5.5–₹9.5 LPA, depending on experience, technical skills, prior CRO/pharma exposure, and the level at which the candidate is hired.

This range is an editorial market estimate and is not an official Phastar salary figure.

Candidates should confirm compensation directly during the recruitment process.

Benefits and Work Environment

According to the job posting, Phastar offers:

• Remote working
• Flexible working hours
• Career development opportunities
• Mentorship
• Continuous learning
• Supportive and collaborative work culture

Phastar’s own career content also highlights professional development, training, mentorship, flexible working arrangements, and exposure to areas such as SAS, R, and clinical data systems.

Why This Role Is Relevant for Clinical Data Management Professionals

This opportunity is particularly relevant for professionals looking to build or advance a career in Clinical Data Management (CDM).

The combination of Medidata Rave, SAS listings, clinical database testing, CDISC, reconciliation, data quality, and clinical-trial operations gives candidates exposure to several important components of modern clinical data management.

The role can also be relevant to professionals progressing toward positions such as:

• Clinical Data Coordinator II
• Clinical Data Coordinator III
• Clinical Data Manager
• Lead Data Manager
• Senior Clinical Data Manager
• Clinical Database Programmer
• Clinical Data Management Specialist

How to Appy

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