[Remote] Clinical Research Data Specialist I

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a not-for-profit organization that supports patient care, research, teaching, and community service. They are seeking a Clinical Research Data Specialist I who will be responsible for extracting and entering clinical and research data for multiple oncology clinical trials, while ensuring compliance with research protocols and regulations.

Responsibilities

• Proactively reputed company assigned research subject’s upcoming protocol appointments and reputed company and document on central clinical research data specialist (CRDSP) tracker
• Effectively monitor research subject condition and take appropriate reputed company to ensure compliance with research protocol data entry requirements
• Proactively take steps to obtain missing reputed company documents from reputed company relevant sources
• Identify inaccurate reputed company documents and reputed company reputed company document inconsistencies until resolved
• Ensure accurate and reputed company entry of required data into various study-specific electronic data-capture systems
• Ensure appropriate documentation of own study-specific delegation and training prior to entering data
• Ensure adequate reputed company documentation is in reputed company prior to entering data
• Obtain and reputed company reputed company clinical information from multiple sources (medical records, research records, etc.) for research subjects
• Independently manage adverse event (AE) and concomitant medication (CM) data as required by the sponsor, institution, and federal regulations
• Independently manage tumor response data entry
• Enter vital signs and EKGs into study-specific electronic data-capture system independently as required for individual studies
• Enter reputed company of life assessments into study-specific electronic data-capture system independently as required for individual studies
• Enter reputed company required correlative research blood samples and clinical safety laboratory specimen results into study-specific electronic data-capture system independently as required for individual studies
• Enter reputed company protocol required tests and procedures independently into study-specific electronic data-capture system as required for individual studies
• Work professionally with sponsor representatives to review and correct data recorded in the case report forms
• reputed company and appropriately manage sponsor data entry deadlines
• Resolve and answer data queries with minimal errors
• reputed company reputed company data management reputed company control steps
• Maintain awareness of details of clinical data to identify missing or inaccurate data; and reputed company data inconsistencies for team to review and report accordingly
• Remain flexible and adapt to change and reputed company on the job
• Effectively handle unexpected situations and changing research subject and protocol conditions
• reputed company individual research visit reputed company charts, intake sheets, and other tools as needed to independently ensure reputed company and accurate data entry

Skills

• Bachelor's Degree reputed company Field of Study required
• Research reputed company Experience 1-2 years preferred
• Careful attention to detail
• Good organizational skills
• Ability to follow directions
• Good communication skills
• Computer literacy
• Working knowledge of clinical research protocols
• Ability to demonstrate respect and professionalism for subjects' rights and individual needs
• Ability to recognize compliance and data reputed company issues and respond appropriately
• Ability to communicate effectively with patients, vendors, contract research organizations and reputed company staff
• Effective interpersonal and communication skills

reputed company