What are the responsibilities and job description for the Clinical Research Coordinator position at Rida Infoways?
Company Description Rida Infoways is a technology-driven company that delivers innovative digital solutions to help businesses grow, transform, and compete effectively in the modern digital landscape. The organization specializes in reliable IT services and customized technology solutions that improve efficiency, strengthen online presence, and drive measurable business results. Its team collaborates closely with startups, small and medium-sized businesses, and enterprises to build scalable digital platforms and long-term growth-focused solutions. Core services include website and e-commerce development, custom software and web applications, UI/UX design, SEO and digital marketing, as well as IT consulting and technical support. Rida Infoways aims to be a trusted global technology partner by providing future-ready, high-quality solutions and turning ideas into powerful digital experiences.
Role Description The Clinical Research Coordinator is a full-time role based in Sheridan, WY, with a hybrid work arrangement that allows some tasks to be completed from home. The coordinator will manage day-to-day clinical research activities, including participant recruitment, screening, and scheduling for clinical trials and research studies. Responsibilities include overseeing informed consent processes, ensuring adherence to study protocols, maintaining accurate source documentation, and coordinating with investigators, sponsors, and regulatory bodies. The role involves collecting and entering data, monitoring study progress, managing study supplies, and supporting regulatory submissions and ethics committee communications. The Clinical Research Coordinator will also help maintain compliance with Good Clinical Practice (GCP), institutional policies, and applicable regulatory requirements while contributing to continuous improvement of research workflows.
Qualifications
Role Description The Clinical Research Coordinator is a full-time role based in Sheridan, WY, with a hybrid work arrangement that allows some tasks to be completed from home. The coordinator will manage day-to-day clinical research activities, including participant recruitment, screening, and scheduling for clinical trials and research studies. Responsibilities include overseeing informed consent processes, ensuring adherence to study protocols, maintaining accurate source documentation, and coordinating with investigators, sponsors, and regulatory bodies. The role involves collecting and entering data, monitoring study progress, managing study supplies, and supporting regulatory submissions and ethics committee communications. The Clinical Research Coordinator will also help maintain compliance with Good Clinical Practice (GCP), institutional policies, and applicable regulatory requirements while contributing to continuous improvement of research workflows.
Qualifications
- Candidates should possess strong clinical research skills, including Clinical Research Experience and familiarity with Clinical Trials.
- Candidates should possess solid protocol-related skills, including understanding and implementing study Protocol requirements and Research methodologies.
- Candidates should possess expertise in participant-facing processes, including managing Informed Consent and ensuring ethical conduct of studies.
- Knowledge of Good Clinical Practice (GCP), FDA and IRB/ethics committee requirements, and basic medical terminology.
- Excellent organizational, documentation, and time-management skills, with attention to detail in data collection and record-keeping.
- Strong written and verbal communication skills for interacting with participants, investigators, sponsors, and cross-functional teams.
- Ability to work effectively in a hybrid environment, managing on-site responsibilities in Sheridan, WY and remote tasks as needed.
- Preferred: Bachelor’s degree in life sciences, nursing, public health, or a related field; certifications in clinical research (e.g., ACRP, SOCRA) are a plus.