Medical Project Coordinator (Mid/Night Shift) | Overnight Jobs HQ
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Lensa

Medical Project Coordinator (Mid/Night Shift)

Lensa

Healthcare Night Shift Full-time

Job Description

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Thermo Fisher Scientific. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

A day in the Life:

  • Coordinates and reviews safety data, utilizing line listings, company dashboard(s) and/or other visualization tools. Reviews data for safety trends, coding consistencies, and potential follow up with investigator sites. Identifies potential issues and resolves or escalates as appropriate
  • Reviews safety data and may provide summations for safety review meetings. May review designated sections of aggregate reports.
  • May help to create/review safety and medical management plan(s) on studies (as applicable) and ensures that the processes included in plan documents are reflective of the contract and services requested.
  • May help Manage routine project implementation, forecasting and coordination, including review of metrics and budget considerations.
  • Monitors the status of the data review and escalates any delays and/or risks to all stakeholders, including study leads.
  • May present at business development, client, and investigator meetings and participate in strategy/business development calls.
  • Resolves complex problems through in-depth evaluation of various factors and offers solutions.
  • May serve as the primary point of contact for clinical/data management project teams.
  • May assist management in training and mentoring.

Education

  • Bachelors degree in Nursing or related Health Sciences (Physician's Assistant) or licensed RN

Experience

  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years), to include 2+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance)

Knowledge, Skills, Abilities

  • Knowledge of GCPs for medical oversight of clinical trials and SAE processing
  • Knowledge of drug development and safety reporting
  • Knowledge of safety data trending to include coding
  • Working knowledge of biostatistics, data management and clinical procedures
  • Strong problem solving and critical thinking skills
  • Good oral and written communication skills
  • Good Strong attention to detail
  • Ability to work in a collaborative team environment
  • Ability to maintain a positive and professional demeanor in challenging circumstances

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

If you have questions about this posting, please contact support@lensa.com

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