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Freshers for Clinical Research jobs (CDM) - Nandis - Bangalore

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Category: Fresher Jobs

Job Requirements

Job Title: Clinical Research Associate (CDM)

Location: Bangalore

Salary: Competitive, based on experience

Qualification: Bachelor's degree in Life Sciences or related field

Work Experience: Freshers

Job Description:

Nandi's is seeking a highly motivated and detail-oriented Clinical Research Associate (CDM) to join our team in Bangalore. This is an excellent opportunity for freshers looking to start their career in Clinical Research. As a CDM, you will manage and analyze clinical trial data to ensure accuracy and compliance with regulatory standards. You will play a crucial role in supporting Nandi's commitment to high-quality clinical research.

Responsibilities:

• Manage and analyze clinical trial data for Nandi's.

• Ensure data accuracy and compliance with regulatory standards.

• Collaborate with the clinical research team to support data management activities at Nandi's.

• Prepare and maintain documentation related to clinical trials.

• Conduct data validation and quality checks.

• Assist in the development and implementation of data management plans for Nandi's.

Requirements:

• Bachelor's degree in Life Sciences or a related field.

• Strong attention to detail and organizational skills.

• Basic knowledge of clinical data management processes.

• Good written and verbal communication skills.

• Ability to work well in a team environment at Nandi's.

• Eagerness to learn and develop in the field of Clinical Research at Nandi's.

Benefits:

• Competitive salary and benefits package.

• Opportunity to work with a leading clinical research organization like Nandi's.

• Professional growth and development opportunities at Nandi's.

• Supportive and collaborative work environment.

• Hands-on experience in managing and analyzing clinical trial data at Nandi's.

Join Nandi's in Bangalore and start your career in Clinical Research. Apply today to be part of a team dedicated to ensuring the accuracy and compliance of clinical trial data.

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