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Senior Clinical Data Manager

08c84dac E79e 44fa 9484 4cd440390eb1 19000101 000001 · Cambridge, MA, US, Cambridge, MA · Active · $144,000–$167,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company08c84dac E79e 44fa 9484 4cd440390eb1 19000101 000001
TitleSenior Clinical Data Manager
Normalized title-
Department / team-
LocationCambridge, MA, United States
Work model-
Employment typeFull Time
Salary$144,000–$167,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-03-31 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from 08c84dac E79e 44fa 9484 4cd440390eb1 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Cambridge.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

Company08c84dac E79e 44fa 9484 4cd440390eb1 19000101 000001
Source3bc242f4-b3c0-49b7-ad56-c269f0dfc936
ATS providerADP Workforce Now Recruiting

Description

PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. We’re driven by our passion for the human aspect of our work and our compassion for the people whose lives have been improved by the innovations we help bring to market. Our clients include national and international biopharmaceutical and medical device companies of all sizes. RESPONSIBILITIES Responsible for all Data Management tasks from study start-up to database lock for assigned studies. Lead multiple large and complex studies, performing and delegating tasks as appropriate. Effectively interact with sponsors and manage vendors. Mentor junior personnel. Develop SOPs and study-specific procedures. Develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, add Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock Procedures Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies Lead, coordinate, and perform User Acceptance Testing (UAT) tasks for complex studies and modules Ensure proper completion of QC and UAT of EDC tools and modules, including database testing, data export testing, and testing of custom programming Coordinate with Sponsor and Vendors to ensure efficiency and quality of electronic data receipt, integration, and reconciliation Troubleshoot technical issues as appropriate Design “smart” listings and study-specific processes for effective data review, query issue and resolution Manage queries and trends to ensure data completeness and integrity Perform coding of adverse events, medical conditions and medications. Perform SAE reconciliation Lead and perform pre-lock and data lock tasks Prepare training materials and user guides for EDC data collection tools, deliver user training Participate in client and team meetings as required, providing status updates and advising on best practices as appropriate Design, generate, and review status metric reports, identifying and communication trends as needed Ensure archiving of study databases and related documents Organize and file study documentation Provide input to cross-functional study timelines and resource requirements to ensure timely completion of project milestones for complex studies Provide regular status updates, keeping cross-functional study team, management, and sponsors informed of any changes Provide study specific training for team members and end users, as appropriate Implement technical solutions, new tools, and resolve complex issues Lead large and complex projects Lead client and team meetings as required Delegate tasks as appropriate, providing mentorship and following through completion Interact with sponsors and manage vendors for complex studies Assist with identification of project scope changes Present at sales and marketing meetings for prospective clients Develop SOPs and manuals EDUCATION Minimum BS in a scientific or health related field or equivalent EXPERIENCE Minimum 9 years of experience in Clinical Data Management SKILLS Knowledge of medical terminology and pharmaceutical notation Expertise with EDC systems, such as Medidata Rave, InForm, Medrio Excellent organizational and time management skills Strong collaboration and leadership skills PHYSICAL REQUIREMENTS Incumbents generally must be able to, with or without accommodation, have the proficient use of both sensory perception/clarity and muscle control/coordination. This may include vision (near, far, color, glare control), hearing (auditory attention, sound localization), speech, strength, agility, dexterity flexibility, steadiness or reaction time. The salary range for this position here noted is representative of a good faith estimate of all experience levels for this position. PROMETRIKA considers several factors when extending and offer, including but not limited to the role, the function and associated responsibilities, the candidate’s work experience, education/training background and parity with current employees in the same or similar positions.

Full job record

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Org ID1496a74c-fa6f-47f4-9947-0299380762da
Source ID3bc242f4-b3c0-49b7-ad56-c269f0dfc936
Board ID3bc242f4-b3c0-49b7-ad56-c269f0dfc936
Provideradp_workforcenow
Provider Job Key564345
TitleSenior Clinical Data Manager
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CountryUnited States
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First Seen At2026-05-31 18:27:52Z
Last Seen At2026-06-06 11:43:19Z
Last Checked At2026-06-06 11:43:19Z
Last Changed At2026-06-06 11:43:19Z
Inactive At—
Source Posted At2026-03-31 18:13:00Z
Source Updated At—
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    "requisitionDescription": "<p><link href=\"https://static.workforcenow.adp.com/mas/mdf-components/24.28.20/styles/froala_editor.pkgd.min.css\" rel=\"stylesheet\" type=\"text/css\"><strong>PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. We&rsquo;re driven by our passion for the human aspect of our work and our compassion for the people whose lives have been improved by the innovations we help bring to market. Our clients include national and international biopharmaceutical and medical device companies of all sizes.</strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.25in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><br></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.25in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><strong>RESPONSIBILITIES</strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.25in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;' id=\"isPasted\">Responsible for all Data Management tasks from study start-up to database lock for assigned studies. Lead multiple large and complex studies, performing and delegating tasks as appropriate. Effectively interact with sponsors and manage vendors. &nbsp;Mentor junior personnel. &nbsp;Develop SOPs and study-specific procedures. </p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;text-indent:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><em>&nbsp;</em></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, add Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock Procedures</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Lead, coordinate, and perform User Acceptance Testing (UAT) tasks for complex studies and modules</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Ensure proper completion of QC and UAT of EDC tools and modules, including database testing, data export testing, and testing of custom programming</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Coordinate with Sponsor and Vendors to ensure efficiency and quality of electronic data receipt, integration, and reconciliation</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Troubleshoot technical issues as appropriate</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Design &ldquo;smart&rdquo; listings and study-specific processes for effective data review, query issue and resolution</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Manage queries and trends to ensure data completeness and integrity</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Perform coding of adverse events, medical conditions and medications.</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Perform SAE reconciliation</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Lead and perform pre-lock and data lock tasks</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Prepare training materials and user guides for EDC data collection tools, deliver user training</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Participate in client and team meetings as required, providing status updates and advising on best practices as appropriate</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Design, generate, and review status metric reports, identifying and communication trends as needed</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Ensure archiving of study databases and related documents</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Organize and file study documentation</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Provide input to cross-functional study timelines and resource requirements to ensure timely completion of project milestones for complex studies</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Provide regular status updates, keeping cross-functional study team, management, and sponsors informed of any changes</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Provide study specific training for team members and end users, as appropriate</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Implement technical solutions, new tools, and resolve complex issues</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Lead large and complex projects</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Lead client and team meetings as required</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Delegate tasks as appropriate, providing mentorship and following through completion</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Interact with sponsors and manage vendors for complex studies</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Assist with identification of project scope changes</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Present at sales and marketing meetings for prospective clients</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Develop SOPs and manuals</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;text-indent:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.5in;text-indent:-.25in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong>EDUCATION</strong></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Minimum BS in a scientific or health related field or equivalent</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;text-indent:0in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.5in;text-indent:-.25in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong>EXPERIENCE</strong></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Minimum 9 years of experience in Clinical Data Management&nbsp;</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.5in;text-indent:0in;font-size:16px;font-family:\"Times New Roman\",serif;'>&nbsp;</p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.5in;text-indent:-.25in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong>SKILLS</strong></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Knowledge of medical terminology and pharmaceutical notation&nbsp;</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Expertise with EDC systems, such as Medidata Rave, InForm, Medrio</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Excellent organizational and time management skills</li><li style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:0in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Strong collaboration and leadership skills&nbsp;</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.5in;text-indent:-.25in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong>&nbsp;</strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:0in;margin-left:.5in;text-indent:-.25in;font-size:16px;font-family:\"Times New Roman\",serif;'><strong>PHYSICAL REQUIREMENTS</strong></p><p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:.25in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'>Incumbents generally must be able to, with or without accommodation, have the proficient use of both sensory perception/clarity and muscle control/coordination. This may include vision (near, far, color, glare control), hearing (auditory attention, sound localization), speech, strength, agility, dexterity flexibility, steadiness or reaction time.</p><p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:.25in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;'><br></p><p style='margin-top:0in;margin-right:0in;margin-bottom:6.0pt;margin-left:.25in;font-size:16px;font-family:\"Times New Roman\",serif;text-align:justify;' data-pasted=\"true\"><em style='box-sizing: border-box; --tw-shadow: 0 0 #0000; --tw-ring-inset: ; --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000; color: rgb(38, 35, 33); font-family: \"Times New Roman\", serif; font-size: 16px; font-variant-ligatures: normal; font-variant-caps: normal; font-weight: 400; letter-spacing: normal; orphans: 2; text-align: start; text-indent: 0px; text-transform: none; widows: 2; word-spacing: 0px; -webkit-text-stroke-width: 0px; white-space: normal; background-color: rgb(255, 255, 255); text-decoration-thickness: initial; text-decoration-style: initial; text-decoration-color: initial;' data-pasted=\"true\"><span style='box-sizing: border-box; --tw-shadow: 0 0 #0000; --tw-ring-inset: ; --tw-ring-offset-width: 0px; --tw-ring-offset-color: #fff; --tw-ring-color: rgba(59,130,246,.5); --tw-ring-offset-shadow: 0 0 #0000; --tw-ring-shadow: 0 0 #0000; font-size: 16px; font-family: \"times new roman\", serif;'>The salary range for this position here noted is representative of a good faith estimate of all experience levels for this position. PROMETRIKA considers several factors when extending and offer, including but not limited to the role, the function and associated responsibilities, the candidate&rsquo;s work experience, education/training background and parity with current employees in the same or similar positions.</span></em></p><p></p>\n",
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