Clinical Research Manager

Clinical Research Manager


We are looking for an enthusiastic, results and performance driven Clinical Research Manager to join our growing team in the medical aesthetics industry!  Based in either Toronto or Boston and reporting to the Senior Director, Product Marketing & Clinical Affairs, the Clinical Research Manager will be responsible for leading all phases of clinical research for new and existing devices.  Clinical Responsibilities range from Concept/Feasibility stages through Regulatory Clearances and Post-Market evaluations. The position collaborates closely with a variety of company entities, including R&D, marketing and regulatory departments.  Worldwide travel as required.  Position can be located in either our Toronto Head Office or home based office in the greater Boston area.

What you’ll do:

  • Prepare clinical development plans for new devices or modifications to existing devices.
  • Identify timelines, resource requirements and budgets for multiple clinical studies.
  • Outline proper study design & documentation including but not limited to Protocol, CRF, ICF, SIV as well as Source and Regulatory documentation as required.
  • Manage process from Study execution through completion, data analysis, summary and creation of scientific papers or abstracts.
  • Ability to Identify/Recommend investigators as well as initiate clinical studies and provide staff training.
  • Monitor clinical investigations, assuring protocol compliance, subject welfare and data integrity.
  • Ensure compliance with Corporate SOPs and Regulatory Authorities
  • Maintain Clinical File structure according to standard GCP policies and regulatory guidance
  • Maintain strong professional relationships with Key Opinion Leaders and Clinical Research sites.
  • Provide expertise and strong leadership and management to direct reports
  • Develop, maintain and motivate team to maximize productivity and efficiency.
  • Promote a sense of teamwork and collaboration with all departments.
  • Ensure QMS, Regulatory and Corporate SOPs are understood and followed by all direct reports
  • Publish department performance metrics and prepare monthly study progress reports
  • Ability to outline/review contracts with consultants, investigators, and CROs.
  • Maintain technical expertise through knowledge of clinical literature, attendance at professional meetings and participation in team meetings.
  • Regular travel to field clinical sites, providing clinical expertise, observation and written reports.
  • Perform other duties as assigned 

What you’ll need:

  • BS, RN or Master’s degree in medical life sciences
  • Five or more years as Clinical Research Associate or equivalent.
  • Minimum 2-3 years in Clinical Research Supervisory role
  • Experience with energy-based aesthetic devices is a plus
  • Strong interpersonal skills in the management and development of employees
  • Excellent analytical, organizational, and problem-solving skills
  • Ability to function as an independent investigator and able to multitask and prioritize tasks
  • GCP or Clinical Trial Design certification (medical device a plus).
  • Complete understanding of Regulatory / GCP guidelines associated with research programs.
  • Must have a valid driver’s license and a valid passport
  • Excellent writing, presentation and communication skills
  • Fluent in English, both written and verbal
  • Flexibility for occasional evening or weekend work, worldwide travel as required (<25%)

 

What you’ll be part of – our Venus Concept Culture:

Venus Concept believes in pushing boundaries while embracing creativity and innovation. Our employees are a critical part of our company’s performance and are at the core of its success. With a focus on entrepreneurship, community involvement, and personal development, we bring a new meaning to work-life balance.  We may be the fastest growing company in the medical aesthetics industry, but we are proud to foster a family-oriented culture.

Venus Concept is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals. Venus Concept is committed to accommodating persons with disabilities. Accommodations are available on request for qualified candidates during each stage of the recruitment process.

About Venus Concept
Venus Concept® is a leading global medical technology company that develops, commercializes, and delivers safe, efficacious, and easy-to-use aesthetic technologies and related practice enhancement services in a unique, industry-disruptive subscription-based business model. Venus Concept's devices have been designed in cost-effective and proprietary ways that enables the company to expand beyond the aesthetic industry's traditional markets of dermatology and plastic surgery, and into non-traditional markets—such as family practice, general practice, internal medicine, obstetrics and gynecology, and medical spas. The company has expanded its subscription platform and is now selling its devices in over 60 countries, including 22 with direct offices. Venus Concept now has over 400 global employees whose customer-centric approach has supported the company's rapid growth. For more information, please visit www.venusconcept.com.

Submit your resume/CV

Thank you for your interest in joining the Venus Concept team. Please fill out the form below and we will get in touch if it's the right match.

ALL FIELDS ARE MANDATORY