Data Analyst

About The Company
MS Clinical Research is a leading organization dedicated to advancing medical knowledge through innovative clinical trials and research initiatives. With a commitment to excellence, integrity, and patient-centric approaches, the company collaborates with global pharmaceutical companies, healthcare providers, and academic institutions to develop new therapies and improve patient outcomes. MS Clinical Research prides itself on maintaining high standards of quality, compliance, and ethical practices, ensuring that all research activities are conducted responsibly and transparently. The organization fosters a dynamic and inclusive work environment that encourages continuous learning, professional growth, and meaningful contributions to the healthcare industry.
About The Role
We are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team. The successful candidate will play a vital role in overseeing the progress of clinical trials, ensuring compliance with regulatory standards, and maintaining the integrity of data collected during studies. This position offers an excellent opportunity for individuals passionate about advancing medical science and making a tangible impact on patient care. The Clinical Research Associate will collaborate closely with investigators, site staff, and cross-functional teams to facilitate smooth trial operations, monitor site activities, and ensure adherence to protocols and regulatory requirements.
Qualifications
Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degrees are a plus.
Minimum of 2 years of experience in clinical research or a related healthcare setting.
Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements.
Excellent organizational and time-management skills with the ability to handle multiple projects simultaneously.
Effective communication and interpersonal skills to liaise with diverse stakeholders.
Proficiency in clinical trial management systems and Microsoft Office Suite.
Ability to travel as required to monitor sites and attend meetings.
Responsibilities
Monitor clinical trial sites to ensure compliance with study protocols, GCP, and regulatory standards.
Conduct site initiation, routine monitoring visits, and close-out visits to ensure proper trial conduct.
Review and verify source documents, case report forms, and other study-related documentation for accuracy and completeness.
Assist in the training and support of site staff regarding protocol procedures and regulatory requirements.
Maintain accurate and detailed records of monitoring activities and site communications.
Collaborate with the project team to address issues, resolve discrepancies, and ensure trial milestones are met.
Support data management activities by ensuring timely and accurate data collection and entry.
Participate in audits and inspections as required, providing necessary documentation and support.
Benefits
MS Clinical Research offers a competitive compensation package along with comprehensive health insurance, including medical, dental, and vision coverage. Employees benefit from a flexible work environment, opportunities for professional development, and a supportive team culture that values innovation and collaboration. The organization also provides paid time off, retirement plan options, and ongoing training programs to enhance skills and career growth. Joining our team means becoming part of a mission-driven organization committed to making a difference in healthcare through cutting-edge research and development.
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, ethnicity, gender, age, sexual orientation, disability, or any other protected status. We believe that a diverse workforce enhances our ability to innovate and succeed in our mission to improve global health outcomes.

Work arrangement
No