Clinical Trial Assistant

6 days ago

Aurangabad Maharashtra, India Vertex Business Solutions Full time

As a Clinical Trial Assistant (CTA) at [Company Name], you will play a crucial role in supporting the successful execution of clinical trials. Working closely with the clinical operations team, you will provide administrative and operational assistance to ensure the smooth conduct of trials from initiation to closeout.

**Key Responsibilities**:

- Maintain accurate and up-to-date trial documentation, ensuring compliance with regulatory standards and internal procedures.
- Assist in the preparation, distribution, and tracking of study-related documents, such as protocols, informed consent forms, and case report forms.
- Collaborate with clinical trial sites to facilitate the timely collection and submission of essential documents.
- Input and maintain clinical trial data in relevant databases, ensuring data accuracy and completeness.
- Assist in the coordination of study-related meetings, including investigator meetings and site initiation visits.
- Stay current with industry regulations, guidelines, and best practices to ensure compliance with applicable standards.

**Qualifications**:

- Bachelor's degree in a relevant field (life sciences, healthcare, or related discipline).
- Previous experience in a clinical trial or research environment is preferred.
- Strong organizational skills and attention to detail.
- Excellent written and verbal communication skills.
- Proficiency in Microsoft Office Suite and familiarity with electronic data capture (EDC) systems.

**Job Types**: Full-time, Fresher

**Salary**: ₹15,020.89 - ₹30,485.07 per month

**Benefits**:

- Cell phone reimbursement
- Health insurance
- Paid sick time

Schedule:

- Day shift
- Monday to Friday

Supplemental pay types:

- Performance bonus

Work Location: In person

**Speak with the employer**

+91 7385000462

  • Clinical Trial Associate

    1 week ago

    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...

  • Clinical Research Associate

    2 weeks ago

    Nagpur, Maharashtra, India Sun Pharma Laboratories Ltd Full time

    **Title**:Clinical Research Associate (Clinical Trials)**: - Date: Oct 8, 2025 - Location: Not Applicable - Company: Sun Pharma Laboratories Ltd **Job Title**: Clinical Research Associate**Business Unit**: Clinical Research**Location**: NagpurAt Sun Pharma, we commit to helping you **“Create your own sunshine”**— by fostering an environment where...

  • Clinical Research Faculty

    2 weeks ago

    Borivali, Mumbai, Maharashtra, India Clinomic Center For Clinical research Full time

    all Clinical Research Topic: - DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 1 DRUG DEVELOPMENT: FROM MOLECULE TO PRESCRIPTION: PART 2 THE EVALUTION OF THE CLINICAL TRIAL PROCESS-A BRIEF HISTORY LESSON HISTORICAL BACKGROUND OF GCPINSTITUTIONAL REVIEW BOARD/INDEPENDENT ETHICS COMMITTEE (IRB/IEC)STAKEHOLDERS ENGAGEMENT TO ENSURE A SUCCESSFUL TRIAL...

  • Clinical Trials Coordinator

    7 hours ago

    Pune, Maharashtra, India Suma Soft Full time

    **About the Role**: We are seeking **enthusiastic and detail-oriented fresh graduates** to join our Clinical Trials Office as **Research Data Coordinators**. This is a fantastic opportunity for recent graduates looking to launch their career in **clinical research**, **healthcare data management**, or **medical data analysis**. **Key Responsibilities**: -...

  • Clinical Trial Psych Rater

    4 days ago

    Mumbai, Maharashtra, India IQVIA Full time

    **Clinical Specialist Consultant -**Assamese**Speaking** **Location**:Remote/virtual** **Hours**:Estimated 10-16h/month** **Role**:Clinical Specialist** **Job Description**: The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability....

  • Clinical Trial Psych Rater

    4 days ago

    Mumbai, Maharashtra, India IQVIA Full time

    **Clinical Specialist Consultant - Punjabi**Speaking** **Location**:Remote/virtual** **Hours**:Estimated 10-16h/month** **Role**:Clinical Specialist** **Job Description**: The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability....

  • Clinical Trial Psych Rater

    2 weeks ago

    Mumbai, Maharashtra, India IQVIA Full time

    **Clinical Specialist Consultant - Marathi**Speaking** **Location**:Remote/virtual** **Hours**:Estimated 10-16h/month** **Role**:Clinical Specialist** **Job Description**: The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability....

  • Clinical Quality Assurance Compliance

    2 weeks ago

    Mumbai, Maharashtra, India, Maharashtra Maxis Clinical Sciences Full time

    Job Title: Clinical Quality Assurance Compliance & trainingExperience: 5 plus yearsLocation: MumbaiType: Full-timeExperience Level: [Senior] Manager/Senior ManagerDepartment: 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...

  • Clinical Research Associate

    1 week ago

    Pune, Maharashtra, India Ascentrik Research Pvt Ltd Full time

    **Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...

  • Clinical Research Associate

    7 hours ago

    Nagpur, Maharashtra, India Clariwell Global Full time

    Assist in setting up, monitoring, and closing clinical trial sites - Ensure that clinical trials are conducted according to protocol, GCP, ICH guidelines, and local regulatory requirements - Perform regular site visits (if applicable) to ensure compliance and data accuracy - Support in the collection and review of essential documents - Communicate with...