Connecting

Senior Clinical Research Associate -SCRA-Auckland NZ

Job Title: Senior Clinical Research Associate -SCRA-Auckland NZ
Contract Type: Permanent
Location: Auckland, New Zealand
Industry:
Salary: $110000 per annum, Benefits: Car+Benefits
Start Date: 2019-06-20
Reference: BH-110523-1
Contact Name: Faiza Khan
Contact Email: faiza.khan@nesgt.com
Job Published: June 21, 2019 06:40

Job Description


Perfect Opportunity for experienced CRA to move into the SCRA role in New Zealand -Auckland .

Clinical Research Associate/Senior Clinical Research Associate (SCRA)


Benefits
  • Generous salary package, car allowance & Bonuses
  • Work within a competitive, niche therapy area
  • Progress quickly, following an industry leading programme
  • Location:Auckland - NZ
  • Reasonable Travel 
  • Work from Home or Office with flexibility.
Qualifications:
  • Must have at least  2+ years for the role CRA and 4 years of Experience for the role SCRA is required in the clinical capacity.
  • Experience should be Including conducting independent monitoring visits, from either a pharmaceutical company or a CRO environment.
  • Full working rights and Valid Visa -
  • (Candidates holding No Work Visa or Full working Rights will not be facilitated by the client)
Role/Description:
  • To perform the activities associated with the site-level feasibility, evaluation, initiation, patient recruitment and retention, monitoring and collection of data, and closeout of clinical trial sites in the geographic area assigned.
  • Responsible for Site management, set up, routine monitoring and close out visits
  • Writing monitoring reports
  • Liaising with investigators and other members of a multi-disciplinary team
  • Variety of therapy areas, which may include oncology, cardiovascular, CNS, respiratory and/or infectious diseases
  • Delivering onsite training of investigators and staff.
  • Monitoring trial progress and ensuring that the project timelines are met.
  • To act as an extension of, and whenever appropriate a surrogate in the field for, the TA study teams and other HQ-based Development Operations functions
  • To align execution activities with agreed-upon project priorities, timelines and quality/productivity specification, in compliance with GCP and local laws and regulations governing the conduct of clinical research.
We provide high-quality employment, competitive salary, excellent working conditions and a personable supportive environment. It is a great chance to join the company that really cares for its people, and invests in their professional development and success.


Apply:Please feel free to contact at faiza.khan @ nesgt. com for more information/Call 02-9696 8008. Faiz a Khan.