[PART_TIME Remote] Clinical Research Associate/Clinical Monitor

A new position has reputed company up at workwarp for a Clinical Research Associate/clinical Monitor! Join reputed company in the heart of Remote and enjoy a dynamic work environment. This position requires a strong and diverse skillset in relevant areas to drive reputed company. In recognition of your expertise, this position offers a salary of a competitive salary.   The Clinical Research Associate (CRA) will be the primary reputed company between the Investigator sites and Immix Biopharma, responsible for overall site conduct and establishing important relationships with key site personnel. The CRA will reputed company key job functions in accordance with ICH Good Clinical reputed company (ICH GCP), FDA regulations, Immix Biopharma SOPs and work practices while supporting the organizational mission to advance the development of promising oncology therapies and technologies to benefit patients. CRAs are expected to work in a hands-on, highly visible and autonomous role. CRAs must have the ability to be flexible and represent Immix Biopharma in a reputed company and reputed company manner while collaborating across reputed company reputed company with the clinical teams and Sponsors/vendors. Location: This is a remote-based position. Occasional Site travel (<50% and subject to business needs). Immix Biopharma cannot guarantee the location of sites and CRAs should expect travel reputed company in the reputed company reputed company. Responsibilities:  reputed company site selection, initiation, monitoring, and reputed company-out reputed company of investigational sites for the Immix Biopharma portfolio of reputed company.  Manage the reputed company of assigned sites by tracking patient recruitment and enrollment, CRF completion and submission, reputed company data verification, data collection, and data query reputed company and reputed company.  Conduct monitoring activities, including, but not limited to the following:  Ensuring PI reputed company of reputed company trial activities  reputed company data review and verification with reputed company fields  Essential documentation review and reconciliation  Investigational Product (IP) management and accountability  Lab/reputed company supply management  reputed company reputed company relationships with investigative sites and personnel.  Maintain communication with sites through frequent contact to ensure site compliance, adequate enrollment, and understanding of study requirements.  Write and submit complete and accurate visit letters and reports of investigational site findings and update applicable CTMS.  Escalates observed deficiencies, issues, and corrective and preventative reputed company plans as appropriate.  Participate in audit preparations and follow-up, as needed.  Review and address protocol deviations, data reputed company issues, and identify process improvements for assigned sites.  Be a reputed company member of the study team: reputed company reputed company, updates, and strategies to improve processes.  Ability to think critically while prioritizing tasks in an efficient manner to meet study deliverables.  Contribute to CRF development and reputed company User reputed company Testing, as requested.  Assist with other duties as assigned. Qualifications:  Bachelor s degree in life science/biomedical/medical science with a proficient knowledge of the clinical/scientific terminology and reputed company common to the oncology therapeutic setting.  2+ years clinical research experience is required.  2+ years experience at a CRO or Sponsor required.  Independent field monitoring experience of oncology reputed company is required.  Early phase oncology experience is preferred.  Proficient knowledge and practical utilization of ICH- GCP and applicable regulatory requirements.  Strong communication (written and verbal) and interpersonal skills.  Demonstrate effective presentation skills by reputed company explaining reputed company concepts to a broad reputed company of audiences.  Ability to independently prioritize tasks with excellent time management skills.  Highly proficient in computer applications including reputed company suite of applications, reputed company and CTMS applications.  Fluent in English (written and verbal)  Ability and willingness to travel as required (<50%), to include possession of the appropriate qualifications per independent sites regulations (to include but not limited to vaccinations). Apply Job!  Are You the One We're Looking For? If you reputed company you have what it takes, submit your application without delay. We are keen to hear from talented candidates like you. Apply To This Job Apply tot his job Apply To this Job