Job Description

medONE is a professionally owned and managed Clinical research organization operating since 2001. We aim to be the "Company of First Choice" as a total solution provider. Renowned for our high-quality control and validation procedures, medONE offers innovative and customizable solutions to meet specialized needs. Our services effectively contribute to clients' work environments, emphasizing the convergence of information technology, clinical processes, advanced medical preparedness, and business processes in the pharmaceutical industry.

medONE is seeking a motivated and detail-oriented Clinical Process Associate to contribute to the success of our clinical trials. If you're passionate about advancing medical research and thrive in a fast-paced environment, we want to hear from you!

As a Clinical Process Associate, you will play a crucial role in supporting the efficient and accurate execution of clinical trials. You will be responsible for a variety of administrative and operational tasks, ensuring compliance with regulatory guidelines and internal SOPs.

Responsibilities:

Assist with the preparation, review, and maintenance of clinical trial documentation (e.g., study protocols, informed consent forms, regulatory submissions).

Maintain and update clinical trial databases and tracking systems.

Coordinate and track the shipment and receipt of clinical trial supplies.

Assist with the scheduling and coordination of site visits and meetings.

Support the preparation of study-related reports and presentations.

Ensure adherence to Good Clinical Practice (GCP) guidelines and company SOPs.

Communicate effectively with internal and external stakeholders.

Assist with the management of Investigator Site Files (ISFs) and Trial Master Files (TMFs).

Assist with the preparation of audit and inspection readiness activities.

Qualifications:

Bachelor's degree in a life science or related field.

Minimum of 1 year of experience in a clinical research setting.

Strong understanding of GCP guidelines and regulatory requirements.

Excellent organizational and time management skills.

Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

Strong attention to detail and accuracy.

Excellent communication and interpersonal skills.

Ability to work independently and as part of a team.

Experience with electronic data capture (EDC) systems (preferred).

Benefits:

Opportunities for professional growth and development.

Collaborative and supportive work environment.

Chance to contribute to cutting-edge medical research.

Job Types: Full-time, Permanent

Pay: ₹22,000.00 - ₹25,000.00 per month

Benefits:

Health insurance
Schedule:

Day shift Monday to Friday
Supplemental Pay:

Yearly bonus
Education:

Bachelor's (Preferred)
Experience:

Clinical research: 1 year (Required)
Work Location: In person

Application Deadline: 25/05/2025