Auriga Research has announced multiple job opportunities for experienced professionals across Medical Writing, Pharmacovigilance, Clinical Data Management and Clinical Operations in Manesar. The openings include Medical Writer, Pharmacovigilance Analyst, Data Management Associate, Project Manager – Clinical Operations, and Clinical Research Associate (CRA) positions.

These Auriga Research jobs 2026 are particularly relevant for candidates with qualifications such as B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Tech, PhD and other relevant Life Sciences degrees, depending on the position.

Most vacancies require previous CRO, pharmaceutical, clinical research, pharmacovigilance, medical writing or clinical data management experience. Candidates should therefore carefully check the role-specific eligibility requirements before applying.

Auriga Research Recruitment 2026 – Overview

Current Openings

1. Medical Writer

Qualification: M.Pharm, PhD or equivalent Life Sciences qualification
Experience: 3–4 years
Salary: ₹6.5–8 LPA

The Medical Writer will prepare scientific and regulatory documents for pharmaceutical, observational and medical device studies.

Key Responsibilities

• Write clinical study protocols, synopses and Clinical Study Reports (CSRs).
• Prepare regulatory and scientific documentation for client submissions.
• Draft quotations and scope-of-work documents for business development proposals.
• Prepare monographs and regulatory dossier content.
• Support scientific manuscript preparation and journal submissions.
• Ensure documents comply with CDSCO, ICH and applicable journal requirements.
• Coordinate document reviews with Clinical Operations, Data Management and Biostatistics.
• Maintain standardized medical writing templates.
• Conduct literature reviews for protocols, manuscripts and scientific documents.

Medical Writer Eligibility

Candidates should possess an M.Pharm, PhD or equivalent Life Sciences qualification with approximately 3–4 years of medical writing experience in a CRO or pharmaceutical organization.

Applicants should have strong scientific writing and English editing skills. Knowledge of ICH E3, Clinical Study Report structure, study protocols, regulatory writing and manuscript preparation is important.

2. Pharmacovigilance Analyst

Qualification: B.Pharm / M.Pharm / Pharm.D
Experience: 3–4 years
Salary: ₹4–6 LPA

This opportunity is suitable for experienced drug-safety professionals with knowledge of ICSR processing, MedDRA coding, literature surveillance and Indian pharmacovigilance regulations.

Key Responsibilities

• Process Individual Case Safety Reports (ICSRs).
• Handle adverse event information and non-standard safety terminology.
• Support Pharmacovigilance Programme of India (PvPI) reporting requirements.
• Conduct literature monitoring for potential product safety signals.
• Support Periodic Safety Update Report (PSUR) preparation.
• Maintain regulatory case-processing and reporting timelines.
• Assist with signal detection and evaluation activities.
• Communicate with clients regarding PV queries and reporting requirements.

Pharmacovigilance Analyst Eligibility

Candidates should have a B.Pharm, M.Pharm or Pharm.D with approximately 3–4 years of dedicated pharmacovigilance experience in a CRO, pharmaceutical company or PV service provider.

Knowledge of ICSR processing, MedDRA, drug safety, regulatory reporting timelines and PvPI is expected.

3. Data Management Associate – Clinical Operations

Qualification: B.Pharm / M.Sc / B.Tech
Experience: 4+ years
Salary: ₹5–6 LPA

The Data Management Associate position focuses on clinical data management, EDC/eCRF review, UAT, data cleaning, query management and database-lock support.

Key Responsibilities

• Review vendor-developed EDC/eCRF databases.
• Participate in build review, UAT and pre-go-live testing.
• Confirm EDC alignment with the clinical study protocol and Data Management Plan.
• Support database go-live readiness.
• Review clinical site data for inconsistencies, errors and missing information.
• Assist site staff with EDC navigation and data-entry queries.
• Manage clinical data query workflows with sites and CRAs.
• Conduct routine clinical data quality checks.
• Support final data cleaning and database lock.
• Extract datasets from EDC systems at defined study milestones.
• Prepare datasets for transfer to Biostatistics.

Clinical Data Management Eligibility

Applicants should have a B.Pharm, M.Sc or B.Tech with at least 4 years of relevant data management experience in a CRO or sponsor organization.

Hands-on experience with at least one major Electronic Data Capture (EDC) platform and experience resolving clinical data queries are important requirements.

4. Project Manager – Clinical Operations

Qualification: Bachelor’s or Master’s in Life Sciences, Pharmacy or related discipline
Experience: 6–8 years
Salary: ₹8–12 LPA

The Project Manager will oversee clinical studies from study start-up through close-out, including timelines, budgets, milestones, sponsor communication and cross-functional coordination.

Key Responsibilities

• Manage end-to-end clinical study timelines and milestones.
• Track study budgets and operational deliverables.
• Serve as a key point of contact for sponsors.
• Coordinate Clinical Operations, Data Management, QA and Pharmacovigilance teams.
• Manage study risks and escalate critical issues.
• Prepare study-status presentations and governance updates.
• Track site payments, vendor invoices and change orders.
• Lead study start-up and site feasibility activities.
• Support contract and regulatory submission planning.
• Coordinate final database lock and CSR timelines.
• Manage study close-out and archival requirements.

Project Manager Eligibility

Candidates should possess a Bachelor’s or Master’s degree in Life Sciences, Pharmacy or a related discipline with approximately 6–8 years of CRO/project management experience.

Experience managing Phase II/III regulatory studies, eTMF, sponsor communication, multi-site clinical trials, budgets and ICH-GCP requirements is preferred.

Note: In the supplied vacancy information, this particular Project Manager listing appears under Arbro Pharmaceuticals, while the other positions are listed under Auriga Research. Candidates should verify the employer/entity details when applying.

5. Clinical Research Associate – Oncology / Medical Devices / Regulatory

Qualification: B.Pharm / M.Pharm / Life Sciences; Nursing or relevant paramedical backgrounds may also be considered
Experience: 3–5 years
Salary: ₹4–8 LPA

The Clinical Research Associate will conduct clinical site monitoring activities and ensure sites comply with protocols, SOPs, ICH-GCP and applicable Indian regulatory requirements.

Key Responsibilities

• Conduct Site Initiation Visits, routine monitoring visits and close-out visits.
• Perform Source Data Verification (SDV) and source-document review.
• Resolve clinical data queries.
• Monitor SAEs, SUSARs and protocol deviations.
• Support CDSCO and Ethics Committee documentation.
• Maintain Investigator Site File (ISF) and Trial Master File (TMF) documentation.
• Communicate with investigators and clinical site teams.
• Monitor subject recruitment, retention and protocol compliance.
• Verify investigational product accountability and storage.
• Support CRF completion and query resolution.
• Escalate clinical site risks and compliance issues.

CRA Eligibility

Candidates should have a B.Pharm, M.Pharm or relevant Life Sciences qualification. Nursing and relevant paramedical backgrounds may also be considered according to the supplied job description.

Approximately 3–5 years of CRA experience is required, including relevant exposure to oncology, haematology or immunology clinical trials.

Candidates should understand ICH-GCP, clinical trial monitoring, SDV, TMF/ISF documentation, CRFs, Indian New Drugs and Clinical Trials Rules 2019, and applicable regulatory requirements.

Who Can Apply?

Depending on the specific vacancy, candidates with the following qualifications may be eligible:

B.Pharm | M.Pharm | Pharm.D | B.Sc/M.Sc Life Sciences | M.Sc | B.Tech/B.E. | PhD | Nursing | Relevant Paramedical Qualifications

Eligibility varies significantly between positions. Candidates should apply only when their qualification, relevant domain experience and technical skills align with the specific job requirements.

Are Freshers Eligible?

No, these vacancies are primarily for experienced candidates.

The supplied positions generally require approximately 3–8 years of relevant experience, depending on the role. Candidates without relevant professional experience should not treat these vacancies as fresher openings.

Why Consider These Opportunities?

These openings provide experienced pharmaceutical and life-sciences professionals with opportunities to work across major clinical research functions, including:

• Pharmacovigilance and drug safety
• Medical and regulatory writing
• Clinical Data Management (CDM)
• Clinical trial monitoring
• Oncology clinical research
• EDC/eCRF and data quality management
• Clinical project management
• Regulatory documentation
• TMF and clinical operations

Experience in these functions can build exposure to multidisciplinary CRO operations and regulated clinical-development processes.

How to Apply for Auriga Research Jobs

Interested candidates should prepare an updated CV highlighting the experience relevant to the position they are applying for.

Application Email: hr@aurigaresearch.com

Application Link – Medical Writer

Application Link – Pharmacovigilance Analyst

Application Link – Data Management Associate (Clinical Operations)

Application Link – Project Manager (Clinical Operations)

Application Link – Clinical Research Associate (Oncology / Medical Devices / Regulatory)