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Clinical Trial Liaison

674a37b7 4b6a 4f38 A5e8 50a609cdab78 19000101 000001 · Lexington, MA, US, Lexington, MA · Remote · Active · $128,000–$142,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company674a37b7 4b6a 4f38 A5e8 50a609cdab78 19000101 000001
TitleClinical Trial Liaison
Normalized title-
Department / team-
LocationLexington, MA, United States
Work modelRemote / Remote
Employment type-
Salary$128,000–$142,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-02-25 / 2026-05-31
Changed / last seen2026-06-06 / 2026-06-06

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PageWhat it containsOpen
Company jobsActive postings from 674a37b7 4b6a 4f38 A5e8 50a609cdab78 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 Lexington.Open
Work model jobsActive Remote postings.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

Company674a37b7 4b6a 4f38 A5e8 50a609cdab78 19000101 000001
Source4f2fb43e-6107-4f34-ab57-87d29ca5c68a
ATS providerADP Workforce Now Recruiting

Description

The Clinical Trial Liaison (CTL) will be accountable for site engagement, communications and timely patient screening / enrollment of assigned sites for Kiniksa’s applicable studies. The CTL will collaborate closely with the Kiniksa Clinical Operations Team, Clinical Development Lead and Medical Affairs as well as the partner CRO for optimal trial execution. The ideal candidate will be self-motivated, with prior hands-on experience in executing clinical trials and a natural ability to build and foster productive relationships with clinical site personnel. This role will require significant travel (75%). The CTL will report to the Associate Director of Clinical Operations overseeing the global site engagement and recruitment strategy for the Clinical Operations department with a dotted line to Regional Clinical Operations Lead of assigned region(s). Responsibilities (including, but not limited to): Be the face of Kiniksa to Investigational Sites taking part in Kiniksa’s applicable studies Delivering on established KPIs related to patient identification, screening and enrollment targets per site and overall Developing and fostering relationships directly with clinical site staff and investigators to understand and address challenges in patient enrollment Developing and maintaining routine communication tools, such as enrollment reports and dashboards, for communicating overall study progress along key metrics, including key risks and challenges, to Senior Management and program team Supporting development and implementation of site-specific engagement plans for maximizing participation at individual clinical sites Supporting qualification, site initiation and/or interim monitoring visits with in-person/remote attendance to help amplify and support patient identification efforts Providing input into and/or developing study related materials to support study participant identification and screening, including support of local clinical site advertising materials Supporting CRO on feasibility and site selection efforts Qualifications: Bachelor’s degree in health or life science; nursing or advanced degree is preferred A minimum of 5 years’ hands-on clinical trial execution experience, with study coordinator experience highly preferred Excellent interpersonal and presentation skills, with a natural ability to establish rapport with a wide range of people Site monitoring and clinical quality compliance experience are strongly preferred Excellent communication skills, including use of MS Office based software tools for the development and maintenance of effective templates to track, monitor and summarize data and key messages for various audiences Strong oral and written communication skills in English Effective project management and risk mitigation skills Demonstrated ability to successfully enroll clinical studies in a timely manner Strong organization skills and demonstrated ability to work independently, navigate within a cross-functional matrix environment, and execute tasks with minimal oversight Ability to travel within the US and outside the US (up to 75%) with potential for overnight stays. Salary is commensurate with experience Kiniksa Benefits Summary - USA The expected salary range for Clinical Trial Liaison is $128,000 - $142,000 annually. Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks. In addition to base pay, this role includes a Bonus plan. Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Full job record

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Org ID952c9fe5-daa7-4a0c-b3f8-5d560f99a753
Source ID4f2fb43e-6107-4f34-ab57-87d29ca5c68a
Board ID4f2fb43e-6107-4f34-ab57-87d29ca5c68a
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Provider Job Key606879
TitleClinical Trial Liaison
Normalized Title
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Department
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Employment Type
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RegionMA
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First Seen At2026-05-31 18:30:04Z
Last Seen At2026-06-06 11:50:59Z
Last Checked At2026-06-06 11:50:59Z
Last Changed At2026-06-06 11:50:59Z
Inactive At
Source Posted At2026-02-25 00:08:00Z
Source Updated At
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    "requisitionDescription": "<div><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:115%;font-size:16px;font-family:\"Aptos\",sans-serif;' data-pasted=\"true\"><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">The Clinical Trial Liaison (CTL) will be accountable for site engagement, communications and timely patient screening / enrollment of assigned sites for Kiniksa&rsquo;s applicable studies. The CTL will collaborate closely with the Kiniksa Clinical Operations Team, Clinical Development Lead and Medical Affairs as well as the partner CRO for optimal trial execution.  &nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:115%;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">The ideal candidate will be self-motivated, with prior hands-on experience in executing clinical trials and a natural ability to build and foster productive relationships with clinical site personnel. This role will require significant travel (75%).&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:115%;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">The CTL will report to the Associate Director of Clinical Operations overseeing the global site engagement and recruitment strategy for the Clinical Operations department with a dotted line to Regional Clinical Operations Lead of assigned region(s). &nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:115%;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&nbsp;</span></p><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:115%;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\"><strong>Responsibilities&nbsp;(including,&nbsp;but not limited to):</strong>&nbsp;</span></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Be the face of Kiniksa to Investigational Sites taking part in Kiniksa&rsquo;s applicable studies&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Delivering on established KPIs related to patient identification, screening and enrollment targets per site and overall&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Developing and fostering relationships directly with clinical site staff and investigators to understand and address challenges in patient enrollment &nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Developing and maintaining routine communication tools, such as enrollment reports and dashboards, for communicating overall study progress along key metrics, including key risks and challenges, to Senior Management and program team&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Supporting development and implementation of site-specific engagement plans for maximizing participation at individual clinical sites&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Supporting qualification, site initiation and/or interim monitoring visits with in-person/remote attendance to help amplify and support patient identification efforts&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Providing input into and/or developing study related materials to support study participant identification and screening, including support of local clinical site advertising materials&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Supporting CRO on feasibility and site selection efforts&nbsp;</li></ul><p style='margin-top:0in;margin-right:0in;margin-bottom:8.0pt;margin-left:0in;line-height:115%;font-size:16px;font-family:\"Aptos\",sans-serif;'><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\"><strong>Qualifications:</strong>&nbsp;</span></p><ul style=\"margin-bottom:0in;margin-top:0in;\" type=\"disc\"><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Bachelor&rsquo;s degree in health or life science; nursing or advanced degree is preferred&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">A minimum of 5 years&rsquo; hands-on clinical trial execution experience, with study coordinator experience highly preferred &nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Excellent interpersonal and presentation skills, with a natural ability to establish rapport with a wide range of people&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Site monitoring and clinical quality compliance experience are strongly preferred&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Excellent communication skills, including use of MS Office based software tools for the development and maintenance of effective templates to track, monitor and summarize data and key messages for various audiences &nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Strong oral and written communication skills in English&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Effective project management and risk mitigation skills&nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Demonstrated ability to successfully enroll clinical studies in a timely manner &nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Strong organization skills and demonstrated ability to work independently, navigate within a cross-functional matrix environment, and execute tasks with minimal oversight &nbsp;</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Ability to travel within the US and outside the US (up to 75%) with potential for overnight stays.</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\">Salary is commensurate with experience</li><li style=\"margin: 0in 0in 8pt; line-height: 115%; font-size: 14px; font-family: arial, sans-serif; color: rgb(0, 0, 0);\"><a href=\"https://www.kiniksa.com/join-us\" rel=\"noreferrer noopener\" target=\"_blank\" title=\"https://www.kiniksa.com/join-us\" style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">Kiniksa Benefits Summary - USA</a></li></ul><p 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; margin-top: 0px; margin-bottom: 1rem; line-height: 1.25; color: rgb(38, 35, 33); font-family: Circular, -apple-system, BlinkMacSystemFont, \"Segoe UI\", Roboto, Oxygen, Ubuntu, Cantarell, \"Fira Sans\", \"Droid Sans\", \"Helvetica Neue\", sans-serif; font-size: 16px; font-style: normal; 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-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\"><span data-pasted=\"true\" 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(0, 0, 0);\">The expected salary range for Clinical Trial Liaison is $128,000 - $142,000 annually. Compensation decisions are based on objective criteria including role responsibilities, experience/qualifications, internal equity, geographic location, and external market benchmarks. In addition to base pay, this role includes a Bonus plan.&nbsp;</span><br 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;\"></span></p><p 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; margin-top: 0px; margin-bottom: 1rem; line-height: 1.25; color: rgb(38, 35, 33); font-family: Circular, -apple-system, BlinkMacSystemFont, \"Segoe UI\", Roboto, Oxygen, Ubuntu, Cantarell, \"Fira Sans\", \"Droid Sans\", \"Helvetica Neue\", sans-serif; font-size: 16px; font-style: normal; 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;'><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-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</span></p></div>\n",
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