Clinical Trial Operations Manager III - OQSIE
Bridgewater, NJ 08807
About the Job
Title: Clinical Trial Operations Manager III
Duration: 03 months contract (Possible extension)
Location: Bridgewater, NJ
This position is not to directly manage trials but does require several years of Clinical Trial Experience in any therapeutic area (Pharma or Biotech)
Please try to stay to the lower end of the rate card
• The TMAIII is responsible for assisting the CTM/CDM/CTOM/TM associates/TL/GL within a Trial
• Operations Group dedicated to a Therapeutic Area BU or across one or more TSUs/DPUs/GMA/USMA,
• etc. in a specific geographical site with the global trial initiation, conduct and reporting of trial
• progress by coordinating and performing assigned operational activities. The TMAIII may need to
• take-on CPA-level administrative tasks as required to meet business needs and to support a
• customer-oriented approach for Trial Operations. Able to mentor CPAs and other TM associates as
• appropriate. Proven ability to proactively identify and propose solutions to operational activities.
• Can manage routine responsibilities autonomously.
Skills:
• Must have TMF / eTMF experience
• Publisher experience is a strong plus
• Knowledge and operational experience working in the clinical trial environment
• Familiarity with Windows-based computer applications (eg, MS EXCEL, ACCESS and Powerpoint)
• and working in clinical trial management systems (eg, IMPACT)
• Excellent interpersonal and communication skills (verbal and written) including good English and
• ability to maintain a high-level of confidentiality
• Self motivated, detail-oriented, ability to handle multiple tasks efficiently and effectively, and
• excellent organizational skills required
• Ability to work effectively in a team
Education:
• Bachelor's degree +6 years of experience in pharmaceutical industry or clinical-related
• discipline including +4 years clinical research experience, familiarity with medical terminology,
• general understanding of the R&D process and previous exposure to GCPs/ICH is required.
• Able to mentor CPAs and other TM associates as appropriate.
• Proven ability to proactively identify and propose solutions to operational activities. Can manage
• routine responsibilities autonomously.
Duration: 03 months contract (Possible extension)
Location: Bridgewater, NJ
This position is not to directly manage trials but does require several years of Clinical Trial Experience in any therapeutic area (Pharma or Biotech)
Please try to stay to the lower end of the rate card
• The TMAIII is responsible for assisting the CTM/CDM/CTOM/TM associates/TL/GL within a Trial
• Operations Group dedicated to a Therapeutic Area BU or across one or more TSUs/DPUs/GMA/USMA,
• etc. in a specific geographical site with the global trial initiation, conduct and reporting of trial
• progress by coordinating and performing assigned operational activities. The TMAIII may need to
• take-on CPA-level administrative tasks as required to meet business needs and to support a
• customer-oriented approach for Trial Operations. Able to mentor CPAs and other TM associates as
• appropriate. Proven ability to proactively identify and propose solutions to operational activities.
• Can manage routine responsibilities autonomously.
Skills:
• Must have TMF / eTMF experience
• Publisher experience is a strong plus
• Knowledge and operational experience working in the clinical trial environment
• Familiarity with Windows-based computer applications (eg, MS EXCEL, ACCESS and Powerpoint)
• and working in clinical trial management systems (eg, IMPACT)
• Excellent interpersonal and communication skills (verbal and written) including good English and
• ability to maintain a high-level of confidentiality
• Self motivated, detail-oriented, ability to handle multiple tasks efficiently and effectively, and
• excellent organizational skills required
• Ability to work effectively in a team
Education:
• Bachelor's degree +6 years of experience in pharmaceutical industry or clinical-related
• discipline including +4 years clinical research experience, familiarity with medical terminology,
• general understanding of the R&D process and previous exposure to GCPs/ICH is required.
• Able to mentor CPAs and other TM associates as appropriate.
• Proven ability to proactively identify and propose solutions to operational activities. Can manage
• routine responsibilities autonomously.
Source : OQSIE