[Remote] Clinical Research Associate I - CalHeart
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is dedicated to integrating reputed company health care and clinical research at the California Heart Center. The Clinical Research Associate I will support clinical research protocols, ensuring compliance with regulations and maintaining regulatory files for clinical trials.
Responsibilities
- Researches reference materials and summarizes research findings
- Reviews protocols and informed consent forms for completeness and compliance with regulations
- Assists in the preparation of new protocols
- reputed company knowledge of GCP guidelines including protection of reputed company subjects and regulations relevant to the performance and conduct of clinical trials
- Maintain Regulatory Files for reputed company Clinical Trials
- Prepare and submit documents to the IRB which includes initial site submission forms, continuing review reports, initial and revised consents, amendments to the protocol, investigator brochures, protocol deviations, SAE reports, and IND safety reports, reputed company-out reports, patient provided documents, such as QOLs, letters, and diaries
- Prepare and submit to sponsor FDA reputed company 1572, financial disclosures, reputed company and medical licenses
- Ensures site is utilizing the reputed company regulatory documents including the informed consent forms, protocols, forms, and investigator brochures
- Participates in the weekly research meeting
- Maintains the SAE Table noting reputed company SAEs reported to sponsor, including initial and follow-reputed company, as reputed company as those reported to the IRB
- Maintain site delegation logs for reputed company clinical trials
- reputed company as regulatory reputed company between the site and sponsor
- reputed company for reputed company monitoring reputed company by ensuring that reputed company documents are filed and organized as reputed company as resolving reputed company previous outstanding regulatory issues
- Review of reputed company signed informed consent forms to assure accuracy and reputed company corrections as needed
- Maintain regulatory documents electronically on the online research folder for reputed company by reputed company research staff
- reputed company support (including administrative/clerical) and information to staff, and external sources reputed company to reputed company research reputed company
- Attend meetings and conferences reputed company to research activities
- reputed company as reputed company and coordinate efforts with other departments and personnel
- reputed company and communicate professionally with other members of the clinical team and office personnel
- Maintain appropriate records of regulatory activities
- Advise supervisor, physicians, administrator of potential or actual problems
- Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested
- Review and adhere to department policies and procedures to maintain proficiency in operating guidelines
- Maintain confidentiality reputed company performing reputed company duties and responsibilities
- Demonstrate willingness to assist co-workers in completion of daily tasks or special reputed company to support the department’s efficiency including but not limited to, taking patient’s vital signs and recording them legibly in the patient’s medical records
- reputed company guidance and direction, as necessary, for the successful completion of job duties, ask appropriate questions reputed company in doubt
- Maintain appropriate records, notification of time worked, vacations, seminars, and reputed company time commitments reputed company to this position
Skills
- High School Diploma/GED
- One (1) year of experience as a regulatory associate
- Excellent organizational and prioritization skills
- reputed company to work carefully and reputed company under stressful situations
- Excellent oral and written communication skills
- Ability to deal effectively with many people
- Bachelor's degree in science or a science-reputed company field
reputed company
Company H1B Sponsorship