1+ months

Clinical Scientist - Remote

WIRB-Copernicus Group (WCG)
Work Remotely

General Information

Location: Remote

Organization: Analgesic Solutions

Job Type: Full Time - Regular

Description and Requirements

The Clinical Scientists at Analgesic Solutions, a subsidiary of WCG support assigned projects by interacting and communicating with industry clients and internal stakeholders to ensure quality and timely delivery of all service offerings. The Clinical Scientist represents Analgesic Solutions' scientific expertise at all external meetings. The Clinical Scientist co-leads all assigned projects with the Executive Director of Clinical Science and Project Management, and collaborates cross-departmentally to ensure the success of the project.

Location:  US Remote

Vaccination Requirement:

To be considered for U.S.-based positions unless currently employed by WCG, where permitted by applicable law (including any applicable reasonable accommodation, medical or religious exemption), candidates must have received or be willing to receive the COVID-19 vaccine by start date.

Education Requirements

  • Graduate degree in a science discipline or other relevant field is required.

Qualifications / Experience:

  • Five years of experience in the clinical research industry required; experience in the area(s) of pain and/or analgesics is preferred
  • Minimum 3 years of experience as a clinical scientist, clinical trial science lead or similar role with client-facing scientific responsibilities
  • Practical knowledge of subjective and objective study endpoints as part of sponsored clinical research is required
  • Ability to function reliably and effectively in a fast-paced, highly detail-oriented environment, and manage multiple projects simultaneously
  • Ability to lead through influencing and negotiating; demonstrated leadership skills and ability to integrate in a team, motivate others and communicate clearly and effectively
  • Strong problem solving/decision making skills, demonstrated by ability for independent critical thinking, solution generation and engagement in active scientific exchange
  • Solid understanding of basic and intermediate research methods and statistics, mastery of spreadsheets and data output, experience with statistical analysis software (e.g., SPSS, R, SQL)
  • Ability to interpret data and explain the importance of the data to different audiences.
  • Strong scientific review and writing skills. Experience authoring scientific journal publications, conference presentations, and/or conference posters is preferred.
  • Demonstrated ability to assess complex situations and devise impact-generating solutions
  • Demonstrated ability to present in front of large audiences from varied backgrounds
  • Strong understanding of Good Clinical Practice (GCP)
  • Knowledge of Placebo Response and patient-reported outcomes is strongly preferred

Essential Duties / Responsibilities:

  • External-facing clinical representative responsible for the independent management of international clinical trials
  • Own scientific responsibility and co-lead each assigned project, along with accountability for ensuring that the scientific integrity is maintained and all necessary analyses are conducted and effectively communicated
  • Actively participate in internal and external project meetings
  • Review, synthesize, monitor, interpret, and address data issues regarding study/site/subject level metrics; present study findings and dashboards to clients by reviewing data, any areas of concern, and recommendations for timely intervention
  • Develop proficiency in multiple proprietary database and dashboard systems
  • Review and/or resolve clinical quality, clinical content, or training-related issues
  • Responsible for conducting site staff training at Investigator Meetings
  • Provide scientific support to external and internal stakeholders, leveraging strong communication and negotiation skills and strategies
  • Respond to and resolve external inquiries regarding clinical content, questions, findings
  • Communicate with all internal stakeholders and coordinate resources to meet project objectives
  • Assist with or take responsibility for the development of project deliverables (e.g., Data Operations Plan, analysis presentations, logs, reports, training content), tailored to clients' needs and SOW
  • QC highly-detailed client-facing deliverables
  • Work with Business Development to review potential studies, RFPs, as needed
  • Develop and nourish peer-to-peer relationships with external consultants, key opinion leaders, and Clinicians, both regionally and in research areas of interest
  • Actively participate in research and publications efforts and report research results externally through peer-reviewed journals, conferences, or other appropriate venues
  • Identify the need for and contribute to the development of departmental and cross-disciplinary work instructions, process guidelines and standard operating procedures to ensure all processes and procedures meet SOP/GCP requirements

Travel Requirements:

  • Occasional travel may be required

#LI - Remote


Posted: 2021-08-02 Expires: 2021-10-04

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Clinical Scientist - Remote

WIRB-Copernicus Group (WCG)

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