Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

Intake Associate

Expired Job

Counsyl South San Francisco , CA 94080

Posted 3 months ago

  • Input and manage patient data from a variety of sources, and ensure that orders are fully processed at the highest level of accuracy

  • Support in the recognition and development of process efficiencies

  • Work closely with a tight-knit team and be prepared to roll up your sleeves to get things done

  • Collaborate with other teams (Customer Success, Billing Operations, EMR, Accessioning) to ensure correct order handling

  • Be the bridge between the laboratory and Customer Success for a seamless customer experience

  • Identify issues and trends and collaborate with your team and leadership to develop best practices to ensure we are providing the best service and experience to all customers

  • Participate in projects that extend beyond your day to day to stretch you to think outside the box or explore new aspects of Counsyl or our customers' experience

About you

  • Associate's or Bachelor's diploma required (or in progress)

  • Exceptional attention to detail and organizational abilities

  • Strong problem-solving skills and ability to make timely decisions in a fast-paced environment

  • Excellent communication skills with the ability to present information in a clear, concise manner

  • Able to prioritize appropriately to get things done

  • Thrive in a dynamic, fast-paced, team-based environment

  • Expert knowledge of Google Apps and Mac OS X

  • Excellent typing skills - must be able to type 70+ wpm and 7,000+ KPH (there will be a test!)

Counsyl, Inc. (the "Company"), a wholly-owned subsidiary of Myriad Genetics, Inc. doing business as Myriad Women's Health, is a leading personalized medicine company dedicated to being a trusted advisor transforming patient lives worldwide with pioneering molecular diagnostics. Myriad discovers and commercializes molecular diagnostic tests that: determine the risk of developing disease, accurately diagnose disease, assess the risk of disease progression, and guide treatment decisions across six major medical specialties where molecular diagnostics can significantly improve patient care and lower healthcare costs. Myriad is focused on three strategic imperatives: maintaining leadership in an expanding hereditary cancer market, diversifying its product portfolio through the introduction of new products and increasing the revenue contribution from international markets. For more information on how Myriad is making a difference, please visit the Company's website: www.myriad.com.

Myriad is an equal opportunity employer and as such, affirms in policy and practice to recruit, hire, train and promote, in all job classifications without regard to race, color, religion, gender, age, sexual orientation, gender identity, national origin, disability status or status as a protected veteran.

Reasonable accommodation will be provided for qualified individuals with disabilities and disabled veterans in job application procedures. We believe that diversity lends a regional, national, and global advantage to the clients we serve. Our workforce consists of dynamic individuals, with a range of backgrounds, talents, and skills.


See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Senior Associate StudyManager (Jp4654)

3 Key Consulting

Posted Yesterday

VIEW JOBS 11/19/2018 12:00:00 AM 2019-02-17T00:00 <strong>Job Title:</strong> Senior Associate Study Manager (JP4654)<br /> <strong>Location:</strong> South San Francisco, CA 94080<br /> <strong>Employment Type</strong>: Contract<br /> <strong>Duration:</strong> 12 months with likely extensions<br /> <strong>Business Unit:</strong> Medical Sciences<br />  <br /> <em>​<a href="http://3keyconsulting.com/">3Key Consulting</a> is looking for a </em>Senior Associate Study Manager  <em>for a leading, international pharmaceutical company headquartered in Thousand Oaks, CA </em><br />  <br /> <strong>Ideal Candidate - </strong><br /> • Phase 1 experience<br /> • Minimum 5 years experience in clinical research management<br /> • Oncology trial experience<br /> • Global trial experience<br /> • Strong scientific background- academic or experience in clinical research setting.<br /> • Protocol writing experience - a plus<br /> • Strong authoring protocols experience in clinical study reports.<br /> <br /> <strong>Responsibilities: </strong> <ul> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Planning, management and reporting of clinical studies conducted by Early Development or the Functional Service</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Provider through oversight of cross-functional study activities</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Identification and resolution of issues</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Communication of study timelines and deliverables ensuring studies are conducted in accordance with SOPs, GCP and regulatory guidance</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Contributing to the First in Human Portal document/Global Development Plan</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Contributing to/authoring protocols, relevant sections of annual safety reports, clinical study reports, and publications</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Management and/or oversight of study budget, timelines and insourcing/outsourcing partners to the required standards<br />  </li> </ul> <strong>Preferred Qualifications: </strong><br /> MS or RN<br /> 7+ years of experience in life sciences or medically related field<br /> 4+ years of bio-pharmaceutical clinical research experience obtained working on industry-sponsored or industry-partnered clinical trials at academic institutions or working on clinical trials in a biotech, pharmaceutical or CRO company<br /> Management experience of direct reports<br /> Experience in oversight of Functional Service Providers, outside vendors (CRO’s, central labs, imaging vendors, etc)<br />  <br /> <strong>Why this position is open: </strong><br /> Backfill for EW that was converted to an Amgen FTE<br />  <br /> <strong>Top 3 Must Have Skill Sets</strong><br /> • Phase 1 experience<br /> • Minimum 5 years’ experience in clinical research management<br /> • Oncology trail experience<br /> • Global Trial experience<br /> • Strong scientific background- academic or experience in clinical research setting.<br /> • Protocol writing experience- a plus<br /> • Strong authoring protocols experience in clinical study reports.<br />  <br /> <strong>Day to Day Responsibilities: </strong> <ul> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Planning, management and reporting of clinical studies conducted by Early Development or the Functional Service Provider through oversight of cross-functional study activities Identification and resolution of issues</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Communication of study timelines and deliverables ensuring studies are conducted in accordance with SOPs, GCP and regulatory guidance</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Contributing to the First in Human Portal document/Global Development Plan</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Contributing to/authoring protocols, relevant sections of annual safety reports, clinical study reports, and publications</li> <li style="padding: 0; margin: 0;" style="padding: 0; margin: 0;">Management and/or oversight of study budget, timelines and insourcing/outsourcing partners to the required standards</li> </ul>  <br /> <strong>Employee Value Proposition: </strong><br /> Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people’s lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world’s leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.<br />  <br /> <strong>Red Flags: </strong><br /> Consistent short tenured positions/jobs<br /> CRO’s are more service providers and are more heavy in the PM side of things and tend to not be best fit.<br />  <br /> <strong>Interview Process: </strong>Telephone and in-person<br /> <br /> We invite qualified candidates to send your resume to <a href="mailto:resumes@3keyconsulting.com">resumes@3keyconsulting.com</a>.<br /> If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com. You are welcome to share this posting with anyone you think might be interested in applying for this role.<br />   3 Key Consulting South San Francisco Ca

Intake Associate

Expired Job

Counsyl