Unicon Pharma Inc ยท 1 day ago
Clinical Trials Management Associate
California, United States
Full-time
Onsite
New Grad, Entry LevelUnicon Pharma Inc is involved in the pharmaceutical industry, and they are seeking a Clinical Trials Management Associate. The role involves conducting site evaluations, ensuring compliance with protocols, and assisting in the coordination of CROs or vendors for clinical trials.
BiotechnologyMedicalPharmaceutical
Hiring Manager
Satish Reddy
Responsibilities
Must meet all requirements for Clinical Research Associate position and have demonstrated proficiency in all relevant areas. With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required:
Assures site compliance with the routine protocol and regulatory requirements and quality of data. Assists in the setting and updating of study timelines
Assists in CRO or vendor selection
With guidance from supervisor coordinates CROs or vendors
Drafts and coordinates review of protocols, informed consents, case report forms and monitoring plans
Assists in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepancies
Participate or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teams (May participate in abstract presentations, oral presentations and manuscript development)
Working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of routine clinical trials
Qualification
Required
Must meet all requirements for Clinical Research Associate position and have demonstrated proficiency in all relevant areas
With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required
Assures site compliance with the routine protocol and regulatory requirements and quality of data
Assists in the setting and updating of study timelines
Assists in CRO or vendor selection
With guidance from supervisor coordinates CROs or vendors
Drafts and coordinates review of protocols, informed consents, case report forms and monitoring plans
Assists in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepancies
Participate or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teams
Working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of routine clinical trials
Company
Unicon Pharma Inc
Unicon Pharma provides customized workforce solutions for life sciences companies, bringing innovative treatments from concept to reality.
Founded in 2013
201-500 employees
H1B Sponsorship
Unicon Pharma Inc has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (71)
2024 (58)
2023 (71)
2022 (80)
2021 (91)
2020 (87)
Funding
Current Stage
Growth StageLeadership Team
Ravi Kollipara
CEO
Company data provided by crunchbase