Clinical Trial Coordinator at Mumbai for Pharma

2 weeks ago


Mumbai, India People Alliance Human Resource Development Foundation Full time

Clinical Trial Coordinator - Mumbai for Pharma Company

**Qualification**:

- A post-graduate in life sciences/PharmD
- GCP trained and Certified

**Required Skills**:

- Thorough understanding of drug development process and expertise in NDCT rules & ICH-GCP/Indian GCP
- Knowledge of clinical trial regulation of US FDA, EMEA, NDCT rules, ICMR guidelines.
- Good leadership qualities and skills.
- Ability to communicate properly between the physician, patient & the site head.
- Assist the Site Head in the managing the Site to ensure ethical conduct of research activities.
- Assist Site Head in evaluates protocols, policies and procedures regarding research projects and studies.
- Maintains pertinent records and documentation.
- Maintenance of Investigator Master File as per good documentation practices & SOP including generation of source documents.
- Oversight of Site Initiation Visit, Monitoring Visits, Site Closeout Visit.
- CRF, e-CRF entry, Data Query resolution.
- Assist the pharmacist in drug accountability and temperature maintaining logs.
- Endow the required file notes, weekly and monthly and monthly report to the reporting authority.
- Tracking the status of all study activities.
- Report to the Site Head daily and take advice for further action.
- Responsible for the Ethics committee activities.
- Coordination of Clinical trial archival documents.
- Coordination Pre-audit, Audit, Post Audit preparation for NABH accreditation.

**Salary**: Up to ₹400,000.00 per year

**Benefits**:

- Cell phone reimbursement

Schedule:

- Day shift

Supplemental pay types:

- Commission pay
- Performance bonus

Ability to commute/relocate:

- New Delhi, Delhi: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- Clinical research: 3 years (preferred)

**Speak with the employer**
+91 7223810246


  • Data Coordinator

    3 weeks ago


    Mumbai, India SUN PHARMA Full time

    Job Title: Database Coordinator (Clinical Research) Business Unit: Clinical Research Location: Mumbai At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As...

  • Medical Writer

    1 day ago


    Mumbai, Maharashtra, India Sun Pharma Laboratories Ltd Full time

    **Title**:Medical Writer (Clinical Trials)**: - Date: Oct 24, 2025 - Location: Sun House - Corporate Office - Company: Sun Pharma Laboratories Ltd **Job Title**: Medical Writer**Business Unit**: Clinical Research**Location**: Sun House, MumbaiAt Sun Pharma, we commit to helping you **“Create your own sunshine”**— by fostering an environment where...

  • Clinical Trials

    3 hours ago


    mumbai, India FIDELITY HEALTH SERVICES Full time

    Company Overview:FIDELITY HEALTH SERVICES is a global pharmacovigilance company focused on patient safety and regulatory compliance. With offices in Toronto, London, Mumbai, Pune, and Ahmedabad, we deliver tech-driven safety and quality solutions to pharmaceutical and biopharmaceutical clients worldwide.Role Summary:Full-time, on-site Clinical Trial –...


  • Mumbai, Maharashtra, India Syneos Health Full time ₹ 6,00,000 - ₹ 18,00,000 per year

    Job Responsibilitiesminimum 2 Years of project management experience.Should have global pharma experience.Candidate from Mumbai location preferred.Develop and coordinate Phase 1 clinical research studies, ensuring all aspects of the study are meticulously planned and executedImplement clinical research protocols and ensure compliance with regulatory...


  • Mumbai, India FIDELITY HEALTH SERVICES Full time

    Company Overview: FIDELITY HEALTH SERVICES is a global pharmacovigilance company focused on patient safety and regulatory compliance. With offices in Toronto, London, Mumbai, Pune, and Ahmedabad, we deliver tech-driven safety and quality solutions to pharmaceutical and biopharmaceutical clients worldwide. Role Summary: Full-time, on-site Clinical Trial –...


  • Mumbai, Maharashtra, India Maxis Clinical Sciences Full time ₹ 1,04,000 - ₹ 1,30,878 per year

    Hiring for Clinical Science Lead - Medical Monitoring for a leading Pharma clientMumbaiTASKS AND RESPONSIBILITIESLead the clinical research medical science related activities such as preparation of synopsis, protocol, Clinical Study Report (CSR) and present the proposals in subjects expert committee (SEC) regulatory meetingCollaborate with clinicians, KOL to...


  • Mumbai, Maharashtra, India Maxis Clinical Sciences Full time ₹ 20,00,000 - ₹ 25,00,000 per year

    Job Title:Clinical Quality Assurance Compliance & trainingExperience: 5 plus yearsLocation:MumbaiType:Full-timeExperience Level:[Senior] Manager/Senior ManagerDepartment:Clinical Research DepartmentPurpose of this Role:This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable...


  • Mumbai, India Maxis Clinical Sciences Full time

    Job Title: Clinical Quality Assurance Compliance & training Experience: 5 plus years Location: Mumbai Type: Full-time Experience Level: [Senior] Manager/Senior Manager Department: Clinical Research Department Purpose of this Role: This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be...


  • Mumbai, India Maxis Clinical Sciences Full time

    Job Title: Clinical Quality Assurance Compliance & training Experience : 5 plus years Location: Mumbai Type: Full-time Experience Level: (Senior) Manager/Senior Manager Department: Clinical Research Department Purpose of this Role: This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be...


  • Mumbai, Maharashtra, India Novartis Full time

    **Summary**: Designs and coordinates the overall direction of clinical development projects. Coordinates activities of associates and investigators to ensure compliance with protocol and overall pre-clinical objectives. Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings. May...