Openings in CRA Fresher's.Hetero • Hyderabad / Secunderabad, Telangana, India

Openings in CRA Fresher's.

Hetero • Hyderabad / Secunderabad, Telangana, India

9 days ago

Job description

Key Responsibilities

Clinical Protocol Review

Assist in the review and understanding of clinical study protocols, informed consent forms, and related study documents.
Support identification of protocol deviations, inconsistencies, and missing information.
Coordinate with senior team members for protocol clarifications and updates.
Maintain accurate documentation as per SOPs and regulatory guidelines.

Literature Search & Medical Writing Support

Conduct systematic literature searches using scientific databases (PubMed, Google Scholar, etc.).
Summarize published clinical data, safety information, and therapeutic background.
Assist in preparing literature review reports, study summaries, and reference documents.
Ensure proper citation and version control of documents.

Clinical Study Monitoring Support

Support clinical trial monitoring activities under guidance, including site documentation review.
Assist in verification of study data, case report forms (CRFs), and essential trial documents.
Help track study progress, timelines, and compliance with GCP and regulatory requirements.
Coordinate with clinical sites, investigators, and internal stakeholders for study-related activities.

Required Skills & Competencies

Basic understanding of clinical research and clinical trial processes.
Knowledge of GCP, ICH guidelines, and regulatory concepts (basic level).
Strong attention to detail and documentation skills.
Good written and verbal communication skills.
Ability to perform literature searches and summarize scientific information.
Proficiency in MS Word, Excel, and PowerPoint.
Willingness to learn and work in a regulated environment.

Skills Required
Gcp, Ms Word, Clinical Research

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Openings in CRA Fresher's. • Hyderabad / Secunderabad, Telangana, India

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