Part-Time Clinical Research Assistant

Benefits

Qualifications

• •Trained in Phlebotomy and Lab processing
• •Strong organizational skills with meticulous attention to detail and accuracy required
• •Excellent written and verbal communication skills required
• •Proficiency in Microsoft Office applications and electronic data management systems required
• •Ability to work independently and collaboratively in a fast-paced environment
• •Commitment to maintaining confidentiality and ethical conduct in clinical research activities
• •3 more items(s)

Responsibilities

• •As a Clinical Research Administrative Assistant, you will play a key role in providing administrative support to our research team and ensuring the smooth operation of clinical trials and research studies
• •You will work closely with research coordinators, operations, regulatory, investigators, and study participants to facilitate the execution of research protocols while adhering to regulatory guidelines and ethical standards
• •Assist with the coordination and scheduling of participant appointments, study visits, and research-related meetings
• •Maintain organized and up-to-date study files, regulatory documents, and participant records
• •Prepare and distribute study-related documents, including informed consent forms, study protocols, and regulatory submissions
• •Assist in the recruitment and screening of eligible participants for clinical trials and research studies
• •Collect, record, and manage data accurately using electronic data capture systems and study databases
• •Communicate effectively with study participants, healthcare professionals, and external stakeholders
• •Provide administrative support to the research team, including document preparation, meeting coordination, and correspondence management
• •Ensure compliance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and institutional policies
• •Collaborate with cross-functional teams to facilitate study start-up, protocol amendments, and study closure activities
• •Perform other duties as assigned to support the efficient operation of clinical research activities
• •9 more items(s)