Qureos Mentor

The START Center for Cancer Research

<div><p>The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering <b>&quot;Hope Through Access&rdquo;</b> to cutting edge trials throughout the United States and Europe.
 </p><p>We are seeking a<b> CTMS Entry Coordinator</b>. This role will assist the Clinical Research Coordinators in all tasks to support their roles. It will require an understanding of research terminology and basic protocol interpretation.
</p><p><b>Work Schedule:</b> Monday-Friday, 8am-5pm</p><p><b>
Location:</b> Myrtle Beach, SC</p><p>
 <b>Essential Responsibilities</b></p><ul><li>
Collect, de-identify, enter/transcribe, and transmit/submit clinical data in paper and/or electronic case reports forms (CRFs), including correction and query resolution for assigned investigational drug studies. This includes but is not limited to images, lab results, and ECGs.
</li><li>Collaborate with Clinical Research Coordinator to ensure data timepoints are accurate and provide query resolution.</li><li>
Contact patients in follow-up as needed per protocol.</li><li>
Review and utilize protocols as guides for study activities for assigned studies.</li><li>
Assist with the setup and formatting of study-specific Eligibility, Study Schedules, and Flow Sheets documents per protocol.</li><li>
Assist with CTMS upkeep, including but not limited to tracking patient visits, IRB re-consents, Serious Adverse Events (SAEs) and Deviations.</li><li>
Ensure that data transmissions remain current for assigned studies.</li><li>
Provide support and information to onsite and remote monitors as necessary.</li><li>
Comply with all applicable regulations, guidelines, and procedures pertaining to data loading, EDC systems, and clinical research.</li><li>
Share responsibility with Data Coordinators to identify lab facilities and normal lab values used for assigned studies so that lab certifications can be requested for the study file.</li><li>
Attend meetings regarding assigned studies as needed, including site initiation visits, Roster meetings and Forms Committee.</li><li>
Communicate as needed with accounts receivable staff regarding transmitted data.</li><li>
Other duties may be assigned at any time.</li></ul><p></p><p><br>
 <b>Required Education and Experience:</b></p><ul><li>
High School diploma or equivalent.</li><li>
One year of research administrative experience within a healthcare, pharmaceutical, or research organization.</li><li>
Knowledge and training in general office administration skills, including computer applications, filing systems, etc.
</li><li>Familiarity with medical terminology.</li><li>
Strong organizational skills and a sense of timeliness in completing projects.</li><li>
Must be detail-oriented and able to understand instructions and work independently.</li></ul><p><b>
 Best-in-Class Benefits and Perks</b></p><p>
We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package&mdash;based on experience&mdash;along with comprehensive benefits designed to support you both personally and professionally:
</p><ul><li>401(k) retirement savings plan with employer match</li><li>
Eligibility for an annual performance bonus, based on role and company results</li><li>
Generous paid time off and paid holidays</li><li>
Comprehensive medical, dental, and vision coverage and optional insurance options</li><li>
Company‑paid life and disability insurance for added financial protection</li><li>
Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one</li><li>
Flexible FSA and HSA plans to support your financial wellness</li><li>
Commitment to a supportive environment that values balance, wellbeing, and flexibility</li><li>
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.</li></ul><p>
 <b>More About START</b></p><p>
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history.</p><p>
 Learn more at STARTresearch.com.
 </p><p><b>Ready to be part of a team changing the future of cancer treatment?</b></p><p>
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.</p><p>
 We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.</p></div><p></p>

CTS Entry Coordinator

<div><p>The START Center for Cancer Research (&ldquo;START&rdquo;) is the world&rsquo;s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering &quot;Hope Through Access&rdquo; to cutting edge trials throughout the United States and Europe.<br>
<br>
The<b> Clinical Research Financial Analyst</b> is<b> </b>responsible for researching and mapping clinical research financials via reporting from START&rsquo;s CTMS system and identification and financial reconciliation of expenses from all participating sites and assist START Accounting in billing. This position plays a critical role in ensuring START can fully capture revenue for services provided, in particular for patient visit variations which require specialized coding and tracking to ensure payment by the clinical trial sponsor.</p><p>
This is a remote role. The annual base salary for this role is<b> $65,000 - $75,000</b>. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. In addition, employees in this role may be eligible for an <b>annual bonus of up to 10%</b> of base earnings.<br>
<br>
<b>Essential Responsibilities</b></p><ul><li>
 Research and map clinical research financials via Advarra Visit Variation Report to contract pricing.</li><li>
 Collaborate with Sponsors and CROs to organize direct invoicing in applicable scenarios.</li><li>
 Work with START Accounting to properly identify direct invoicing scenarios and indicate on necessary trackers.</li><li>
 Participate in larger reporting projects that assist in identification of rogue or potential erroneous trial expenses.</li><li>
 Attend Revenue Cycle task meetings with Leadership and Study Teams in order to align with CTMS visions and changing landscape.
</li><li> Work with Clinical site operations teammates and systems (ARIA) to provide necessary detail for sponsor billing and payment.</li><li>
 Assist in streamlining the mapping and reconciliation process to assist with company growth and scaling.</li><li>
 Other duties may be assigned at any time.
</li></ul><p><b>Required Education &amp; Experience</b></p><ul><li>
 Bachelor&rsquo;s degree in financial or business administration field (Accounting, Finance, Business Administration, or similar field).</li><li>
 Minimum of one year of CTMS experience, or equal experience of education and knowledge.</li><li>
 Clinical Trial Management System (OnCore specific) experience</li><li>
 MS Office Excel and other MS Office programs.</li></ul><p><b>
Preferred Education and Experience:</b></p><ul><li>
 Coding knowledge (CPT, HCPCS).</li><li>
 Three years of CTMS experience, in a healthcare or clinical research setting (Oncology experience) or equal experience of education and knowledge.</li><li>
 Three years Clinical Trial Management System (OnCore specific) experience.</li></ul><p><b>
Physical &amp; Travel Requirements:</b></p><ul><li>
Sitting: Must be able to sit for extended periods of time.
</li><li>Prolonged use of computer, keyboard, and mouse.
</li></ul><p><b>Best-in-Class Benefits and Perks</b><br>
We value our employees&rsquo; time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:</p><div><div><ul><li><p>
401(k) retirement savings plan with employer match</p></li></ul></div><div><ul><li><p>
Eligibility for an annual performance bonus, based on role and company results</p></li></ul></div><div><ul><li><p>
Generous paid time off and paid holidays</p></li></ul></div><div><ul><li><p>
Comprehensive medical, dental, and vision coverage and optional insurance options</p></li></ul></div><div><ul><li><p>
Company paid life and disability insurance for added financial protection</p></li></ul></div><div><ul><li><p>
Employee Assistance Program (EAP) providing confidential, no cost support for you and your family from day one</p></li></ul></div></div><div><div><ul><li><p>
Flexible FSA and HSA plans to support your financial wellness</p></li></ul></div><div><ul><li><p>
Commitment to a supportive environment that values balance, wellbeing, and flexibility</p></li></ul></div><div><ul><li><p>
We&rsquo;re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you&rsquo;ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.</p></li></ul></div></div><p></p><p><b><br>
More about The START Center for Cancer Research</b></p><p>
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world&rsquo;s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of &ldquo;Hope Through Access&rdquo;. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda &ndash; one of the most effective cancer drugs in medical history.</p><div><p>
Learn more at STARTresearch.com.</p></div><p><b><br>
Ready to be part of a team changing the future of cancer treatment?</b><br>
Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online.<br>
<br>
We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.</p></div>

Clinical Research Financial Analyst (Remote)

Join The START Center for Cancer Research and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

The START Center for Cancer Research

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CTS Entry Coordinator

Clinical Research Financial Analyst (Remote)