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Clinical Research Coordinator Job in Rishikesh | Pharma Jobs in India

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Looking for pharma jobs in India? Explore this exciting Clinical Research Coordinator opportunity with a reputed organization offering strong growth in pharmaceutical careers.

About the Company

HRAPL is a growing organization in the clinical research and pharmaceutical domain, known for its commitment to regulatory compliance and quality-driven operations.

The company focuses on delivering high standards in clinical trials while ensuring adherence to global guidelines like ICH-GCP.

With a strong emphasis on innovation and operational excellence, HRAPL continues to expand its footprint in India’s clinical research landscape.

The organization provides a professional environment that supports learning, collaboration, and long-term career growth.

Job Details

  • Company Name: HRAPL
  • Experience: 3–4 Years
  • Qualification: Life Sciences / Biotechnology / Pharmacy or related fields
  • Location: Rishikesh, Uttarakhand
  • Work Type: On-site

Job Description

HRAPL is hiring for a Clinical Research Coordinator role to support clinical trial site operations.

The position involves managing patient workflows, ensuring accurate documentation, and maintaining compliance with study protocols.

Clinical Research Coordinator

  • Department: Clinical Research
  • Market: India
  • Role: Clinical Research Coordinator (CRC)
  • Experience: 3–4 Years
  • Education/Qualification: Graduate in Life Sciences, Biotechnology, Pharmacy, or related fields

Skills/Qualifications

  • Strong knowledge of ICH-GCP guidelines
  • Experience in clinical trial site operations
  • Proficiency in patient coordination and workflow management
  • Skilled in ICF (Informed Consent Form) handling
  • Expertise in essential clinical documentation
  • Ability to coordinate with investigators and CRAs
  • Good communication and organizational skills
  • High attention to detail and compliance

Key Responsibilities

  • Manage daily clinical trial site activities
  • Coordinate patient visits and follow-ups
  • Ensure accurate and timely documentation
  • Handle ICF process and compliance
  • Maintain study-related records and files
  • Coordinate with CRAs and investigators
  • Ensure adherence to study protocols
  • Support audit and inspection readiness

Benefits/Perks

  • Strong career growth in pharma jobs
  • Exposure to clinical research operations
  • Competitive salary package
  • Learning and development opportunities
  • Collaborative work environment
  • Industry-relevant experience

How to Apply

Interested candidates can apply by sending their updated resume to:

Email: contact@hrapl.in

Subject Line Format: Name_CRC_Rishikesh

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Apply now and take the next step in your pharmaceutical career.

Why You Should Join

Joining HRAPL offers a chance to work in a structured and compliance-driven clinical research environment.

Employees gain hands-on exposure to real-world trials, enhancing their expertise in regulatory and operational aspects.

The company fosters continuous learning, teamwork, and professional growth.

It is an ideal workplace for candidates aiming to build long-term careers in clinical research and pharmaceutical industries.

FAQs

What is the eligibility for this role?

Candidates must have a degree in Life Sciences, Biotechnology, Pharmacy, or related fields with 3–4 years of experience.

How can I apply for this job?

You can apply by emailing your resume to contact@hrapl.in with the specified subject line.

Is this a walk-in interview?

No walk-in interview details are provided. This is an email-based application process.

What career growth opportunities are available?

The role offers growth in clinical operations, regulatory exposure, and advancement in pharmaceutical careers in India.

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