Veeda Clinical Research has announced new clinical research jobs in Ahmedabad for professionals interested in Clinical Operations and Medical Writing. The company is currently recruiting for two positions: Clinical Research Associate (CRA) and Medical Writer.

These Veeda Clinical Research jobs offer opportunities for pharmacy professionals with relevant experience in clinical trials, site monitoring, ICH-GCP, clinical documentation, protocol development, and Clinical Study Report (CSR) writing.

For the Clinical Research Associate job, Veeda is seeking candidates with 3–7 years of experience, while the Medical Writer job requires 2–6 years of experience. B.Pharm candidates are eligible for both opportunities based on the job information provided.

Veeda Clinical Research Vacancy Overview

Role 1: Clinical Research Associate

The Clinical Research Associate (CRA) job at Veeda Clinical Research focuses on off-site clinical monitoring, site initiation, feasibility activities, study documentation, regulatory compliance, site training, and audit support.

Candidates should have practical clinical research experience and a sound understanding of ICH-GCP guidelines, clinical trial monitoring, site initiation and site feasibility.

Key Responsibilities – Clinical Research Associate

• Conduct off-site visits during different phases of clinical studies according to the approved study plan.
• Conduct Initial Site Visits and train or guide site personnel on study requirements.
• Verify protocol-specific prerequisites and confirm that clinical trial sites are ready for study activities.
• Conduct routine monitoring visits at predetermined frequencies according to study guidelines.
• Coordinate Feasibility Assessment Questionnaires and obtain required information from potential clinical trial sites.
• Follow up regularly with off-site nodal personnel and study teams.
• Prepare Pre-study Qualification Reports, Site Initiation Visit Reports, Site Monitoring Visit Reports and Site Closeout Visit Reports.
• Obtain essential documents such as calibration reports, agreements and other study-specific documentation from sites and vendors.
• Provide logs, forms, source data templates, recruitment trackers and feasibility questionnaires to study teams.
• Ensure clinical trial data is recorded and maintained according to required formats.
• Review study-related documentation for compliance with SOPs, protocols and applicable regulatory requirements.
• Train and mentor off-site teams on study protocols, GCP, Root Cause Analysis and updated regulatory requirements.
• Respond to observations and queries raised during internal QA/QC reviews and sponsor or regulatory audits.
• Support overall compliance with clinical trial protocols and applicable regulations.

CRA Qualification & Experience

Education: B.Pharm or M.Pharm in any specialization.

Experience: 3–7 years of relevant experience.

Candidates should preferably have experience or knowledge in:

• Clinical Research
• Clinical Operations
• Clinical Trial Monitoring
• Site Monitoring
• Site Initiation
• Site Feasibility
• ICH-GCP
• Clinical Trials
• Regulatory Compliance
• Clinical Documentation

Role 2: Medical Writer

The Medical Writer job at Veeda Clinical Research involves the preparation and review of critical clinical trial and regulatory documents, including protocols, Investigator Brochures and Clinical Study Reports.

The position requires strong scientific writing and documentation skills along with an understanding of clinical trials and regulatory requirements.

Key Responsibilities – Medical Writer

• Prepare and review clinical study protocols, ICDs, study synopses and other study-specific documents.
• Prepare and review Investigator Brochures.
• Support preliminary and detailed feasibility assessments for patient-based clinical studies.
• Conduct scientific and reference literature searches for assigned projects.
• Provide protocol training to monitors and clinical trial site teams when required.
• Prepare and review Clinical Study Reports for phase clinical trials conducted by the Clinical Operations department.
• Coordinate with Project Managers to complete clinical documentation according to defined project timelines.
• Prepare Full CSRs, Abbreviated CSRs, Synoptic CSRs, CSR shells and Interim Reports according to sponsor requirements.
• Support preparation of clinical documents intended for CTD/eCTD regulatory submissions where applicable.
• Review Statistical Analysis Plans, mock shells and table, figure and listing specifications for appropriate content.
• Perform literature reviews to obtain relevant scientific and clinical background information.
• Support sponsor audits and regulatory inspections, including inspections involving authorities such as the US FDA, EMA and Indian regulators.
• Assist with responses to regulatory queries and deficiencies.
• Write, edit and manage high-quality clinical documentation in accordance with company standards and regulatory guidelines.
• Prepare and review departmental SOPs as required.
• Ensure reports, appendices and associated documentation are archived or electronically archived within applicable timelines.
• Prepare project summaries for submission to the reporting head or designee when required.
• Develop and maintain document templates, formats and styles that meet internal, sponsor and regulatory requirements.
• Participate in process improvement and departmental training initiatives.

Medical Writer Qualification & Experience

Education: B.Pharm in any specialization is explicitly listed in the provided job posting.

Experience: 2–6 years.

Relevant skills include:

• Medical Writing
• Clinical Study Reports
• Protocol Writing
• Investigator Brochure
• Clinical Trials
• Literature Review
• Clinical Documentation
• Regulatory Writing
• CTD/eCTD
• Life Sciences
• Pharmacovigilance
• Medical Devices

Why Consider Veeda Clinical Research Jobs?

These openings can be relevant for experienced pharmacy and clinical research professionals seeking career growth in clinical operations or medical writing.

The CRA position provides exposure to clinical site monitoring, site initiation, feasibility, ICH-GCP compliance, audits and clinical operations. The Medical Writer role provides experience with protocols, Investigator Brochures, CSRs, literature reviews, regulatory documentation and inspection support.

The advertised compensation is approximately ₹3.5–5.5 LPA for the CRA role and ₹3–5.5 LPA for the Medical Writer role, according to the supplied listings. Actual compensation may depend on experience, skills and the employer’s final offer.

How to Apply

Application Link For Clinical Research Associate

Application Link For Medical Writer