Quality Assurance Analyst-PACE, Clinical - Riverside

Under the direct supervision of the Care Management (CM) Program Manager and the general supervision of the Chief Clinical Nursing Officer (CCNO), this role will be instrumental in ensuring data accuracy and identifying eligible care management members. · ...

Looking for someone strong in Spotfire with R-scripting experience or good experience in clinical data management reporting and Project management. · Minimum 3 years of experience, preferably within medium-large pharma or CRO, developing reports/dashboards in TIBCO Spotfire. · St ...

We know you re here to find a place where you can grow be supported and feel valued so here s what we bring to the table: · Competitive compensation $90 000 – $93 000 per year · Student loan repayment assistance/refinancing Receive $3 000 annually through GRADIFI and consolidate ...

We're more than a workplace — we're a community. Every day, we unite passion and purpose to support children teens and adults with developmental disabilities.We work as a team celebrate each other's wins and are committed to helping every client and team member reach their full p ...

We're more than a workplace — we're a community. Every day, we unite passion and purpose to support children, teens, · and adults with developmental disabilities.We work as a team, · celebrate each other's wins, · Treat every client · & family with care,respect,& understanding. · ...

+ $90,000 – $93,000 per year · Student loan repayment assistance/refinancing – Receive $3,000 annually through GRADIFI and consolidate loans at a competitive rate · In-house CEU events plus $1,000 CEU reimbursement · Health benefits: · Medical, Dental,and Vision (company cover ...

+We are seeking a Senior Clinical Supervisor to lead and inspire our team of Behavior Interventionists and Assistant Clinical Supervisors. This role involves providing supervision and mentorship, developing individualized treatment plans, collaborating with the team, delivering p ...

The primary responsibility of the Clinical Data clinical data analyst is to support CDM study start-up activities · Developing database specificationsAuthoring and executing test scriptsPreparing key CDM deliverables ...

The primary responsibility of the Clinical Data clinical data analyst is to support CDM study start‐up activities, · Define and specify clinically data collection requirements (e.g., eCRFs, CRFs) for assigned studies. · Maintain and develop assigned sections of Data Management de ...

We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients' lives. · As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to increase access ...

As the Clinical Device Management Associate Analyst, you will support device processes associated with clinical trials. · You will also ensure compliance with regulations and manage the lifecycle of device inventory and accountability to support clinical trials. · ...

We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations · Analyze clinical device data · Notify cross functional team members for data updates/changes · ...

The Clinical Research Finance Analyst will interface directly with business partners in the pharmaceutical and medical device industries to administer accounts receivable for a large clinical trial portfolio. · Administer accounts receivable for a large clinical trial portfolio. ...

Job Summary:Experience with CDM study startup activities will be prioritized. ...

We are looking for Senior Clinical Data Management Analyst for our client in Irvine, CA · Define and specify clinically data collection requirements (e.g., eCRFs, CRFs, edit checks and collection of external data) for assigned studies; including defining, performing, and coordina ...

The primary responsibility of the Clinical Data clinical data analyst is to support CDM study startup activities. · ...

The Clinical Trial Device Management Analyst will support device processes associated with clinical trials. · Partner with stakeholders to manage inventory and device accountability for sites · Ensure clinical sites are sufficiently set up and stocked with trial supplies and tra ...

The primary responsibility of the Clinical Data analyst is to support CDM study startup activities including developing database specifications authoring and executing test scripts and preparing key CDM deliverables. · ...

Clinical Trial Device Management Analyst supports device processes associated with clinical trials ensuring compliance with regulations managing lifecycle of device inventory accountability. · ...

The primary responsibility of the Clinical Data Analyst is to support CDM study start-up activities including developing database specifications authoring and executing test scripts and preparing key CDM deliverables · Define specify clinically data collection requirements e.g. e ...