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Surgical Science Liaison

Coloplast

Minneapolis, MN · HybridFull-time$103–150K/yrSeen todaySeen in employer's feed today

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At a glance

Compensation
$103–150K/yr
Location
Minneapolis, MNHybrid
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Master's degree

Job overview

The Surgical Science Liaison connects scientific initiatives with stakeholders, partnering with investigators and research sites and translating scientific data across R&D, Clinical Affairs, Marketing, and other teams. The role supports study design, publications, site training, scientific education, and external engagement. It is described as full-time and remote, with frequent office time in Minneapolis or Arlington and anticipated travel of 50%.

Skills & qualifications

RequiredNice to have

Skills

Surgical AnatomySurgical ProceduresTissue-Based Medical DevicesClinical Study Protocol WritingScientific Research MethodologiesClinical Development ProcessesInterpersonal SkillsRelationship BuildingScientific CommunicationPublication WritingPublication Review and EditingAnalytical ThinkingCritical ThinkingInformation SynthesisScientific Talking PointsStatistical AnalysisResearch Study Design

Qualifications

Advanced Scientific DegreeMaster's or Ph.D. In Relevant Scientific Field2+ Years Industry ExperiencePhysician and KOL Experience

Full job description

Job Duties

Surgical Science Liaison

Location:

US

Job Family:

Quality Assurance

Country/Region:

United States

The Surgical Science Liaison serves as the bridge between our organization's scientific initiatives and key stakeholders. This role provides executive-level scientific partnership to Principal Investigators (PIs) and research sites. This role translates complex scientific data between R&D, Key Opinion Leaders (KOLs), Clinical Affairs, and Marketing to drive innovation and ensure scientific accuracy in all communications, both written and oral. The SSL will be called on to draft and edit scientific publications, work with the Trial Council to refine protocol proposals, engage with the medical community regarding proposals for scientific studies and actively present, persuade, and defend technology with a comprehensive understanding of published data.

This role is a full-time remote role with dedicated time in either our Arlington, VA or Minneapolis, MN office, reporting to the Director of Clinical Development. While this role can be remote, we are looking for someone who can be in our Minneapolis, MN or Arlington, VA offices frequently.

Major Areas of Accountability

Lead study design discussions with Health Care Providers (HCPs) and Clinical Development team for Randomized-Controlled Trials (RCTs) and Investigator-Initiated Studies (IISs)

Manage manuscript writing process and submission process, contribute to the writing process and support medical professionals involved in the writing process

Facilitate site training for RCTs and IISs, provide overall study design support

Develop and maintain relationships with HCPs and Key Opinion Leaders (KOLs) to gather scientific insights for Clinical Development studies and key strategic initiatives

Identify and evaluate research ideas from the field, conducting preliminary analysis before presenting to clinical development teams

Translate complex research findings into accessible training materials for medical affairs and sales teams

Partner with Marketing to ensure scientific accuracy and integrity in core messaging

Synthesize scientific data to support development of educational content and materials

Stay current with scientific developments in relevant therapeutic areas

Represent the company at scientific conferences and professional meetings

Facilitate scientific exchange between external experts and internal teams

Provide scientific expertise to cross-functional teams when needed

Work cross-functionally between R&D, Clinical Development, Medical Education & Marketing departments

Anticipated travel: 50%

Kerecis employees are required to conduct business to the highest ethical and professional standards; comply with applicable laws and regulations, the Advamed Code of Ethics on Interactions with Healthcare Professionals, and company policies

Other job duties as assigned

Basic Qualifications

Advanced scientific degree in relevant scientific field (e.g., life sciences, biochemistry, pharmacology, or related discipline) from an accredited college or university

Knowledge of surgical anatomy, and surgical procedures with tissue-based medical devices

Understanding of and experience in writing clinical study protocols

Strong understanding of scientific research methodologies and clinical development processes

Excellent interpersonal and relationship-building skills

Superior communication abilities, with talent for translating complex scientific concepts for diverse audiences

Demonstrated ability to build collaborative relationships with researchers and healthcare professionals

Willingness and ability to write, review, edit and guide publications to demonstrate the scientific product benefits

Strong analytical and critical thinking skills

Ability to synthesize information from multiple sources and to utilize that to write compelling scientific publications

Ability to boil down key publication takeaways into key talking points for sales and Medical Affairs team

Preferred Qualifications

Master's or Ph.D. in relevant scientific field (e.g., life sciences, biochemistry, pharmacology, or related discipline) from an accredited college or university

2+ years of experience in pharmaceutical, biotechnology, or medical device industry

Experience working with physicians, Key Opinion Leaders and other medical professionals within the relevant field

Familiarity with statistical analysis and design experience for research studies

Base Salary Range: $103,000 - $150,000

This job description is intended to set forth the core functions required for this position and describe the general nature of the work to be performed. It may not contain a comprehensive inventory of all duties, responsibilities, and qualifications required of employees to do this job. Job duties, responsibilities and activities may change or be supplemented at any time as necessary. Kerecis is an Equal Opportunity Employer.

61750

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EOE M/W/Vets/Disabled

Minimum Education Required

High School Diploma or Equivalent

Minimum Experience Required

2 - 20 years

Shift

First (Day)

Number of Openings

1

Public Transportation Accessible

Yes

Veterans Encouraged to Apply

No

Physical Required

Yes

Drug Test Required

Yes

Compensation

$11.41 / Hourly

Postal Code

55411

Job Type

Full Time

Place of Work

On-site

Requisition ID

61750

Job Benefits

Not specified

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