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Skills: Medical Preprints, Reporting Standards, Analytical Skills, Organizational Skills, Prioritization
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$47k–$78k/yr
Full-time
Posted 1d ago
~40 hrs/week
Remote in Maryland, United States
Responsibilities
Oversee the operation of medical preprint queues to ensure turnaround times are met and harmful content is prevented. Collaborate with journal partners and internal teams to align editorial policies and reporting standards.
Requirements
Preferred experience of 1 year working with medical preprints and familiarity with medical reporting standards. Requires strong analytical and organizational skills with the ability to work independently.
Full job description
SSRN is Elsevier’s preprint server, working with over 1,200 Elsevier journals to offer submitting authors the option to preprint their research. Authors may also submit directly to SSRN through a journal‑independent de novo route.
One of SSRN’s recent successes has been strong growth in the clinical and medical disciplines, supported by notable partnerships such as Preprints with The Lancet and Cell Press journals. This growth coincides with the emergence of new funder policies that require authors to preprint their work and meet specific compliance criteria.
In this role, you will oversee the smooth operation of the medical queues, ensuring turnaround times are met and that all required reporting standards—including ethical information—are satisfied. You will also be responsible for ensuring that no potentially harmful preprints are posted. Occasional managerial oversight will be provided for complex situations and cases. Working closely with the Content Director, identify gaps in contractor coverage so that additional resources can be recruited, maintaining queue performance and health. In addition, you will deliver reporting on growth within the medical area and contribute to projects that promote excellence in medical preprinting.
• Responsibilities:
Oversee the smooth running of the medical queues such that turnaround times are met
Prevent the posting of medical preprints that may cause harm and ensure that appropriate ethics, funding and COIs are provided.
Work with journal partners such as Preprints with The Lancet to support their editorial policies as well as working on any reporting and / or projects.
Liaise with the Content Director over funders and their policies and how it affects SSRN policies and liaising on policy changes as needed.
Liaise with the Production and Product teams over changes in policies and approaches for identifying bad content in the medical and life science disciplines
Preferred Skills and Experience:
1 years’ experience of working on medical preprints and familiarity with reporting standards on medical papers is preferred
• Self- Starter and happy working independently or as part of a team
• Able to understand and advocate for the need of authors and readers.
• Strong analytical, organizational and prioritization skills
• Ability to work methodically, problem-solving and fact-checking
• Preferred understanding of preprint submission workflows. Be able to work with operations and production to accomplish shared goals.
Primary Location Base Pay Range: Home based-Maryland $46,700 - $77,700.
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Regulatory compliance and product data management solutions for medical device manufacturers and pharmaceutical labelers
Industry
IT Services and IT Consulting
Company size
5,001-10,000 employees
Founded
1961
Headquarters
Horsham, Pennsylvania
LinkedIn followers
7,796
Healthcare relies on regulatory product data submissions for quality, safety, reliability and transparency, benefitting the entire supply chain. Reed Tech is proud to play a role as both a regulatory consultant and technology partner. Meet FDA and other global health authorities' submission requirements with confidence. Reed Tech offers data conversion, publishing, electronic submissions and content management solutions for the life sciences industry.
Offices: 7 Walnut Ave, Horsham, Pennsylvania 19044, US
UDIGlobal Data Synchronization NetworkSPLLDR for BiologicsMedical Device Data ManagementDrug Product Data ManagementMedical Device Safety and QualityGlobal UDI submissionsDrug Label ResearchGUDID UDI
Regulatory compliance and product data management solutions for medical device manufacturers and pharmaceutical labelers
Industry
IT Services and IT Consulting
Company size
5,001-10,000 employees
Founded
1961
Headquarters
Horsham, Pennsylvania
LinkedIn followers
7,796
Healthcare relies on regulatory product data submissions for quality, safety, reliability and transparency, benefitting the entire supply chain. Reed Tech is proud to play a role as both a regulatory consultant and technology partner. Meet FDA and other global health authorities' submission requirements with confidence. Reed Tech offers data conversion, publishing, electronic submissions and content management solutions for the life sciences industry.
Offices: 7 Walnut Ave, Horsham, Pennsylvania 19044, US
UDIGlobal Data Synchronization NetworkSPLLDR for BiologicsMedical Device Data ManagementDrug Product Data ManagementMedical Device Safety and QualityGlobal UDI submissionsDrug Label ResearchGUDID UDI