Associate, NCDR Research Studies

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    "ShortDescriptionStr": "The Research Study Manager will serve as the project manager and primary point of contact for a portfolio of registry-based research studies for the National Cardiovascular Data Registry (NCDR).  This individual will support the complete lifecycle of research studies by assisting in the development of study protocols, drafting contractual agreements, and ensuring the timely completion of study milestones by collaborating with a cross functional team to ensure high quality client deliverables. This role requires an individual with strong attention to detail, broad cardiovascular clinical knowledge and analytic skills with an engaging, collaborative, and client-focused approach to working with a multitude of internal and external stakeholders.",
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    "ExternalDescriptionStr": "<p>The Research Study Manager will serve as the project manager and primary point of contact for a portfolio of registry-based research studies for the National Cardiovascular Data Registry (NCDR). &nbsp;This individual will support the complete lifecycle of research studies by assisting in the development of study protocols, drafting contractual agreements, and ensuring the timely completion of study milestones by collaborating with a cross functional team to ensure high quality client deliverables. This role requires an individual with strong attention to detail, broad cardiovascular clinical knowledge and analytic skills with an engaging, collaborative, and client-focused approach to working with a multitude of internal and external stakeholders.</p>",
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    "CorporateDescriptionStr": "<div>\n <p>At the American College of Cardiology, we bring our hearts to work.</p>\n <p>We are a 500-person organization dedicated and committed to our mission to transform cardiovascular care and improve heart health for all for more than 75 years. When you join our team, you become part of a culture that envisions a world where science, innovation and knowledge optimize cardiovascular care and outcomes.</p>\n <p>Every day, we are committed to supporting our more than 60,000 members and their patients around the globe and in doing so, ensure our staff have a positive environment of teamwork, collaboration, professionalism and excellence. To learn more about why ACC has been recognized as a great place to work, please visit our site, <a href=\"https://www.acc.org/jobs\" target=\"_blank\" rel=\"nofollow\">www.acc.org/jobs</a>.</p>\n <p><b>What We Offer:</b><br>\n   ACC values all members of our College family, including ACC staff. As the foundation of the organization, ACC staff enjoy world-class benefits and a culture of work-life balance. Our benefit offerings include insurance (medical, dental, vision, basic life, and short- and long-term disability, and supplemental options), generous paid time off (pre-loaded vacation and sick, 12 holidays and an organizational shut-down during the last week of the year, parental leave, 2 community service days, and half-day summer Fridays), tuition assistance and a very competitive 10% retirement contribution after a year of service, and much more! You can visit our careers site for an overview of our <a href=\"https://ibyrjb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/ACCJobs/jobs\" target=\"_blank\" rel=\"nofollow\">full offerings.</a>&nbsp;Please note that these offerings may change at any time.</p>\n <p>ACC believes in fair and equitable pay. Multiple factors are taken into consideration when we determine what salary to offer a selected candidate. These factors include, but are not limited to, the scope and responsibilities of the role, the selected candidate’s work experience, education and training, as well as internal equity, market, and business considerations. Our salary ranges differ based on the cost of labor in the local market where the job will be performed.<br>\n   The salary ranges for will vary based on the local labor market; ACC’s Recruitment Team will be able to provide more information to candidates during initial discussions.</p>\n <p><b>EEOC:</b><br>\n   ACC is proud to be an equal opportunity and affirmative action employer. We celebrate diversity and are committed to creating an inclusive environment for all candidates and employees. All employment is decided on the basis of qualifications, merit and business need. Equal Opportunity Employer, including individuals with disabilities and veterans. ACC is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, you may contact Katie Sarreal, HR Business Partner at [email protected]&nbsp;or (202)375-6351.</p>\n</div>",
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    "ExternalResponsibilitiesStr": "<ul><li>Serve as study manager for FDA, NIH and industry-sponsored and investigator-initiated research studies by implementing reliable methods to support clinical research activities.</li><li>Contribute scientific, clinical, data, and technical expertise to guide the execution of complex research projects. &nbsp;This includes, but is not limited to:<ul><li>Leading research focus interactions with clients in the medical device and pharmaceutical industries and provide clinical registry expertise and guidance to support custom data analytics and research study requests.</li><li>Reviewing inbound research questions, requests, and study protocols to determine the feasibility of conducting studies within the context of the NCDR infrastructure.</li><li>Working closely with physician members, and member committees to facilitate clinical, scientific, and strategic review of new research proposals.&nbsp;</li><li>Work closely with the data analytics team and data analytics centers to review and assess the suitability of research proposals</li><li>Work closely with the data analytics team and data analytics centers to facilitate the completion of accepted projects.</li><li>Drafting study procurement documents that accurately capture the scope of work to be performed and translate client requests into statements of work, project budgets, and project contracts.</li><li>Coordinating the activities of internal and external cross-functional teams and monitor the progress of study milestones and deliverables, ensuring quality and timeliness of project deliverables.&nbsp;</li><li>Preparing and submitting IRB applications.</li><li>Ensuring alignment of budgets with study needs and responsible for invoicing and tracking revenue and expenses for the life of the study.&nbsp;</li><li>Preparing and submit project status and effort reporting to stakeholders, including federal agencies, industry, committees, and internal staff.</li></ul></li><li>Represent ACC on internal and external groups, as assigned. Build and maintain excellent relationships with internal and external partners and clients.</li><li>Anticipate risk and identify challenges early on and communicate project risk as well as possible risk solutions to Team Lead.<ul><li>Work with internal IT teams, NCDR registry product managers and others as appropriate to ensure the logic and application of registry data for various study types. Serve as a liaison between ACC registry management teams and external research partners</li></ul></li></ul>",
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