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Surgical Science Liaison

Role overview

Qualifications

  • Advanced scientific degree in relevant scientific field (e.g., life sciences, biochemistry, pharmacology, or related discipline)
  • 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

Responsibilities

  • 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

Key facts

  • Remote from: United States
  • Full time
  • Mid-level (2-5 years)
  • English

Other skills

  • Analytical Skills
  • Critical Thinking
  • Relationship Building
  • Social Skills
  • Verbal Communication Skills

About the company

Coloplast logo

Coloplast

Medical Devices & Equipment

Coloplast develops products and services to make life easier for people with deeply personal and private medical conditions. These conditions are often associated with trauma and taboo. The more intimate the condition, the greater the requirement to come closer to customers, understand their world and develop solutions that are sensitive to their special needs. We call this intimate healthcare. Closeness to all customers makes this possible. We listen to better understand needs and respond by finding new ways to do things better together. We lead the way by bringing the best ideas first and fast to market in the form of medical devices and service solutions. Deeply private and personal medical conditions are our focus. Our passion to make a real difference to people’s lives is what drives and unites us. Our culture supports high ambitions and releases the full potential of our own people to achieve them. Our business includes Ostomy Care, Continence Care, Wound & Skin Care, Interventional Urology and Voice & Respiratory Care. We operate globally, employing more than 14,500 people.

Company details

Company typeXLarge
IndustryMedical Devices & Equipment
Company size10001

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Job description

 

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. 

 

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Marcus Rivera

Chief Revenue Officer

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