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Description andRequirementsJOB SUMMARY:The Clinical Scientist supports assigned projects by interacting and communicating with investigative sites, study sponsors, andinternal stakeholders to ensure quality and timely delivery of all clinical service offerings. The Clinical Scientist represents WCG scientific expertise at allexternal meetings. The Clinical Scientist co-leads all assigned projects with ProjectManagement and collaborates cross-departmentally to ensure the success of the project. EDUCATIONREQUIREMENTS:Graduate degree in a life science discipline or other field relevant to the business focuspreferred.Bachelors degreerequired. QUALIFICATIONS/EXPERIENCE:Fiveyears of experience in the clinical research industryrequired; experience working for a biopharmaceutical sponsor or a clinical research organizationpreferred.Minimum 3years of experience as a clinical scientist, clinical trial sciencelead, clinical site educator/supervisor or similar role with client-facing scientific responsibilities.Minimum 4years of experience with the administration and/or training of rating scales with practical knowledge of study endpoints as part of sponsored clinical research isrequired.Ability to function effectively in a fast-paced environment andmanagemultiple projects simultaneously.Ability toleadthrough influencing and negotiating; demonstratedleadership 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.Strong communication and negotiation skills across audiences with a demonstrated ability to assess complex situations and devise impact-generating solutions based on incomplete data.Demonstrated ability to present in front of large audiences from varied backgroundsrequiring the ability to tailor the discussion to meet their needs.Fluent in English; bi-lingual or multi-lingual skills arepreferred.Strong understanding of Good Clinical Practice (GCP). ESSENTIAL DUTIES/RESPONSIBILITIES:To perform thisjobsuccessfully, an individual must be able to perform each essential duty and responsibility satisfactorily. Therequirements listed below are representative of the knowledge, skills, and/or abilityrequired. External facing clinical representative responsible for the independent clinicalmanagement ofinternational 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 and remediations are conducted and effectively communicated.Actively participate ininternal andexternal project meetings (e.g., weeklyexternal client call, Investigators meetings).Review, monitor, and proactively address issues regarding study level metrics; present study dashboards to sponsors by reviewing data, any outliers or areas of concern, as well as any actions taken to address these concerns.Resolve clinical quality or training related issues.Responsible for the calibration of clinical team, conduct rater training events, and remediations as specified in the study-specific training plans.Provide scientific support toexternal andinternal stakeholders, leveraging strong communication and negotiation skills and strategies.Respond to and resolveexternal inquiries regarding WCG scoring or (link removed)municate with allinternal stakeholders and coordinate resources to meet project objectives.Assist with or take responsibility for the development of project deliverables (e.g., scale verification, electronic form development, training materials for in-person or online training, etc.).Work with Business Development to review potential studies, RFPs, as needed.Develop and nourish peer-to-peer relationships withexternal consultants, key opinionleaders, and clinicians, both regionally and in research areas of interest.Actively participate in research and publication efforts and report research resultsexternally through peer-reviewed journals, conferences, or other appropriate venues.Identify the need for and contribute to the development of departmental and cross-disciplinarywork instructions, process guidelines and standard operating procedures to ensure all processes and procedures meet SOP/GCPrequirements.Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.Proficient knowledge of MS Office, specifically Word, Excel, PowerPoint and the ability to produce detailed reports and presentations using these tools.Attendance and punctuality are essential functions of the position.Ability to provide documentation allowinginternational travel. TRAVELREQUIREMENTS:This role mayrequire up to 20% travel which may be domestic orinternational, including overnight and weekend stays, consistent with project needs and office location. EXPECTED ANNUAL BASE SALARY:$87,480 to$136,000GPS LEVEL: P4 #HP#LI-REMOTE#LI-JK1 WCG is proud to be an equal opportunity employer Qualified applicants will receive consideration for employment without regard to race, color, national origin or ancestry, religion or creed, sex, sexual orientation, genderidentity, age, marital status, disability, genetic information, citizenship, veteran status, reprisal or any other legally recognized basis or status protected by federal, state or local law.