About The Company

MS Clinical Research is a leading organization dedicated to advancing medical science through innovative clinical trials and research initiatives. With a commitment to excellence, integrity, and scientific rigor, MS Clinical Research collaborates with global pharmaceutical companies, healthcare providers, and academic institutions to develop new therapies and improve patient outcomes. Our state-of-the-art facilities, experienced team, and patient-centric approach position us as a trusted partner in the clinical research industry.

We prioritize ethical standards, compliance, and transparency in all our operations, ensuring that our research contributes meaningfully to the medical community and benefits society at large.

About The Role

We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our dynamic team. In this role, you will be responsible for managing and coordinating clinical trial activities to ensure smooth execution and compliance with regulatory standards. You will serve as a vital link between investigators, participants, and regulatory bodies, ensuring that all trial procedures are conducted accurately and ethically.

Your role will involve overseeing patient recruitment, data collection, documentation, and adherence to study protocols. The ideal candidate will possess strong organizational skills, a thorough understanding of clinical research processes, and the ability to work collaboratively in a fast-paced environment. This position offers an excellent opportunity to contribute to groundbreaking medical research and gain valuable experience in the clinical trials industry.

Qualifications The ideal candidate should possess a Bachelor’s degree in Life Sciences, Nursing,



Pharmacy, or a related field. A minimum of 2 years of experience in clinical research or a healthcare setting is preferred. Familiarity with Good Clinical Practice (GCP) guidelines, regulatory requirements, and clinical trial management systems is essential. Strong communication skills, attention to detail, and the ability to multitask are critical for success in this role.

Certification in clinical research or related areas, such as CCRP (Certified Clinical Research Professional), is advantageous. Candidates should demonstrate a proactive approach to problem-solving and possess the ability to work effectively both independently and as part of a team.

Responsibilities

- Coordinate and oversee all aspects of clinical trial activities, ensuring compliance with study protocols, regulatory standards, and company policies.
- Assist in patient recruitment, screening, and enrollment processes to meet study enrollment targets.
- Maintain accurate and complete documentation of trial activities, including case report forms, source documents, and regulatory files.
- Communicate effectively with investigators, sponsors, and regulatory agencies to facilitate trial progress and resolve issues promptly.
- Ensure proper training of staff involved in the clinical trial and monitor adherence to study procedures.
- Manage inventory, supplies,



and equipment necessary for clinical trial activities.
- Participate in monitoring visits, audits, and inspections to ensure compliance and readiness.
- Support data collection, entry, and verification processes to maintain data integrity and quality.
- Assist in preparing progress reports, study updates, and regulatory submissions.
- Stay updated on industry regulations, guidelines, and best practices related to clinical research.

Advantages MS Clinical Research offers a comprehensive benefits package designed to support our employees' well-being and professional growth. Employees enjoy competitive salary packages, health insurance coverage, and paid time off. We provide opportunities for ongoing training and development to enhance your skills and career trajectory. Our supportive work environment fosters collaboration, innovation, and respect. Additionally, employees have access to wellness programs, flexible working arrangements, and employee recognition initiatives. Joining our team means being part of a forward-thinking organization committed to making a difference in healthcare through groundbreaking research.

Equal Opportunity

MS Clinical Research is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based on race, gender, age, religion, sexual orientation, disability, or any other protected characteristic. We believe that a diverse workforce enhances our ability to innovate and serve our community effectively. All qualified applicants are encouraged to apply and will be considered based on merit and experience.

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