Clinical Research Coordinator

MaximaTek; India; Remote; INR 6,220,000 - 8,612,000; Part time

Job summary

A research support company in India is seeking experienced Clinical Research Coordinators for remote roles in US shifts. Ideal candidates should have over 7 years of experience in clinical study coordination, possess strong organizational skills, and a Bachelor's degree or equivalent. Responsibilities include managing study subjects, assisting with regulatory submissions, and acting as a liaison with sponsors. This position offers both part-time and full-time opportunities in a compliance-driven environment.

Qualifications

• 7+ years of relevant clinical research coordination experience.
• Compliance with medical surveillance and training requirements.
• Familiarity with clinical research environments.
• Ability to work with patients and human research subjects.

Responsibilities

• Manage study subjects including screening, enrollment, and treatment.
• Assist with eligibility assessments and obtaining informed consent.
• Act as liaison with sponsors and external research sites.
• Support sample collection, processing, and storage activities.
• Assist with regulatory submissions and protocol review.
• Maintain study documentation and regulatory files.
• Provide cross-functional support to research teams.

Skills

Strong organizational skills

Effective written communication

Effective verbal communication

Ability to work with patients

Education

Bachelor’s degree or equivalent

Job description

🚀 We’re Hiring: Clinical Research Coordinators (Remote | US Shift | Part-time/Full-time)

MaximaTek is looking for experienced Clinical Research Coordinators with 7+ years of experience to join our growing research support team. If you have a strong background in clinical study coordination and enjoy working in a dynamic, compliance-driven environment, we’d love to connect with you.

Responsibilities

• Manage study subjects including screening, enrollment, and treatment in compliance with regulatory guidelines and SOPs
• Assist with eligibility assessments and obtaining informed consent
• Act as a liaison with sponsors and external research sites
• Support sample collection, processing, and storage activities
• Assist with regulatory submissions, protocol review, and monitoring
• Maintain study documentation, regulatory files, and Study Manager data entries
• Provide cross-functional support to research teams and short-term projects

Minimum Qualifications

• Bachelor’s degree or equivalent combination of education and experience
• Strong organizational, written, and verbal communication skills
• 7+ years of relevant clinical research coordination experience
• Ability to work with patients and human research subjects
• Compliance with medical surveillance and training requirements
• Exposure awareness to clinical research environments and safety protocols

Maxima Solutions Pvt. Ltd. is an equal opportunity employer committed to building an inclusive and high-performing workforce.

📩 Interested candidates can share their resumes at: [e-mail]

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