Clinical Study Manager

Clinical Study Manager
  • $0.76 - $66.19 per Hour
    HOUR
  • Temporary
  • Research Triangle Park NC, US Research Triangle Park WAKE US 27560
Job Ref: JO000103636
Sector: Science
Date Added: 29 July 2020


Clinical Study Manager

Basic Qualifications: Bachelor Degree in Life Sciences. Prior GSK experience with prior HIV experience is highly desirable. Minimum of 5 years of experience from a CRO or Pharma working in clinical research, or clinical operations roles in the conduct of multi-center, international, clinical studies. (Examples are Study Manager, Clinical Research Scientist, Study Operations Leader). Understanding of running clinical trials and clinical training and/or applicable clinical research experience. Knowledge of using clinical trial master file (TMF) systems (paper or electronic) and associated business processes Knowledge of Trial Master File industry accepted standards, such as the DIA’s TMF Reference Model. Excellent working knowledge of International Conference on Harmonization/ Good Clinical Practice (ICH/GCP) regulations for sponsor study records. Excellent interpersonal and communication skills, including the ability to establish and maintain effective working relationships with customers, peers and stakeholders. Proven record of being customer driven, ability to learn processes quickly, a self starter, and able to work in independently as well as in matrix team environment. Analytical / logical, with superior organizational skills and attention to details, addresses assignments in a timely and efficient manner.
Key Responsibilities: Support the responsible clinical scientists in the operational conduct of clinical studies by assisting with all aspects of the maintenance of clinical studies. These will include ensuring uninterrupted supply of study medication, appropriate safety monitoring, data collection, reporting of regulatory agency required updates, participating in identifying and implementing solutions to combine clinical studies from various programs into rollover trial(s). Ensures effective management of the study plan including all activities, budget, and timelines and other related duties as assigned. Ensures effective communications with Staff in the regions/countries with regards to study conduct.

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SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

SRGTalent
29/08/2020 12:00:00
USD 0.76 0.76
Contact Consultant:
Jamison McClam

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