Accede Clinicals Hiring Clinical Research Coordinator

Accede Clinicals Hiring Clinical Research Coordinator at AIIMS Raipur

Clinical research opportunities at major hospital sites remain one of the most practical entry points for pharmacy and life science professionals. Accede Clinicals has announced immediate hiring for the role of Clinical Research Coordinator (CRC) at the AIIMS Raipur clinical trial site, offering a valuable opportunity for candidates with 1–2 years of clinical trial experience.

Site‑based clinical research roles are increasingly important as hospitals conduct more investigator‑initiated and sponsor‑driven clinical studies. For professionals from pharmacy, biotechnology, and life science backgrounds, the CRC role provides hands‑on exposure to patient coordination, regulatory documentation, and real clinical trial operations.

Working at a prestigious government medical institution such as AIIMS also gives professionals direct experience with investigators, sponsors, and clinical research associates involved in regulated clinical studies.

Company Overview

Accede Clinicals is a clinical research support organization providing services related to clinical trial coordination, site management, regulatory documentation, and study execution support. The company collaborates with investigators, hospitals, and sponsors to ensure clinical studies are conducted according to international research standards.

Organizations like Accede Clinicals help clinical trial sites maintain proper documentation, regulatory compliance, and efficient patient recruitment during research studies. By supporting site operations, these teams contribute to the safe and ethical conduct of clinical trials that ultimately lead to the development of new therapies.

With the increasing number of pharmaceutical and medical research studies being conducted across India, site management and clinical coordination roles are becoming essential to successful study execution.

Career Outlook for Clinical Research Coordinators in 2026

The clinical research industry in India continues to expand as pharmaceutical companies and biotechnology firms conduct more clinical trials across hospitals and academic medical centers. By 2026, professionals with practical experience in site management, patient coordination, and clinical documentation will remain in strong demand.

Clinical Research Coordinators serve as the operational backbone of clinical trial sites. They help ensure that patient enrollment, informed consent procedures, and regulatory documentation are handled accurately and ethically.

Professionals who begin as CRCs often progress into roles such as Senior Clinical Research Coordinator, Clinical Trial Manager, Site Manager, Clinical Research Associate (CRA), or Clinical Operations Specialist within CRO organizations and pharmaceutical companies.

Job Role & Responsibilities

The Clinical Research Coordinator will manage day‑to‑day clinical trial activities at the site while ensuring strict adherence to study protocols and regulatory guidelines.

Key responsibilities include:

• Coordinate clinical trial activities between investigators, study teams, and sponsors
• Manage patient scheduling, screening, and follow‑up visits during clinical studies
• Handle informed consent form (ICF) documentation and patient coordination
• Maintain essential clinical trial documentation and site regulatory files
• Ensure compliance with study protocols and Good Clinical Practice guidelines
• Support monitoring visits conducted by Clinical Research Associates
• Maintain accurate patient records and trial documentation
• Assist investigators and site staff with study related operational tasks

The role requires strong attention to detail and the ability to manage multiple responsibilities while maintaining high standards of patient safety and regulatory compliance.

Eligibility / Qualifications

Candidates applying for this clinical research opportunity should meet the following criteria:

• Graduate degree in Life Sciences, Biotechnology, Pharmacy, or related discipline
• 1–2 years of experience in clinical trial site operations
• Knowledge of clinical trial documentation and patient coordination
• Understanding of ICH‑GCP guidelines and study protocol compliance
• Ability to coordinate with investigators, Clinical Research Associates, and site teams

Relevant education backgrounds include: B.Pharm, M.Pharm, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Life Sciences, M.Sc Clinical Research, M.Sc Biotechnology.

Location & Salary

Location: AIIMS Raipur, Chhattisgarh, India

Salary: Competitive compensation based on experience and site responsibilities. Clinical trial site roles often provide strong exposure to real clinical research environments, which can significantly enhance long‑term career opportunities in CROs and pharmaceutical companies.

Immediate joiners may receive preference during the recruitment process.

Application Process

Interested candidates can submit their updated CV to the recruitment email provided below.

Email Application:

hr.ac808@gmail.com

Applicants should highlight their experience in patient coordination, clinical trial documentation, and ICH‑GCP compliance while applying.

Candidates available for immediate joining may have an advantage during the selection process.

Frequently Asked Questions

Who can apply for the Clinical Research Coordinator role at Accede Clinicals?
Candidates with degrees in life sciences, biotechnology, pharmacy, or related disciplines with 1–2 years of clinical research experience can apply.

What does a Clinical Research Coordinator do?
A CRC manages site operations during clinical trials, coordinates with patients and investigators, maintains regulatory documentation, and ensures study protocol compliance.

Is ICH‑GCP knowledge required for this role?
Yes. Basic knowledge of ICH‑GCP guidelines and clinical trial documentation is important for clinical research site roles.

What career growth opportunities exist for CRC professionals?
Clinical Research Coordinators can advance into roles such as Senior CRC, Clinical Trial Manager, Clinical Research Associate (CRA), or Clinical Operations Manager.

Summary

Category	Details
Company	Accede Clinicals
Vacancies	Clinical Research Coordinator
Required Education	B.Pharm, M.Pharm, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, M.Sc Clinical Research
Experience	1–2 years in clinical trial site operations
Location	AIIMS Raipur, Chhattisgarh
Department	Clinical Research / Site Operations