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Senior Clinical Research Associate 2 - Single Pharma Sponsor

Job Title: Senior Clinical Research Associate 2 - Single Pharma Sponsor
Contract Type: Permanent
Location: Sydney, Australia
Industry:
Salary: $120000 - $127500 per annum
Start Date: 2019-01-13
Reference: BH-97354
Contact Name: Christopher Parkinson
Contact Email: christopher.parkinson@nesgt.com
Job Published: January 13, 2019 22:00

Job Description

A passionate CRO with unmatched career development into a Project Management path is looking for a SCRA2 to join them and focus on a single sponsor where appropriate.
They will be glad to welcome you to their great team, and achieve new heights together.

The scope of responsibilities will include:
  • Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
  • Site management, general administration of clinical research studies in Australia.
  • Contact for clinical investigators, vendors and support services in regard to study progress
  • Monitoring trial progress and ensuring that the project timelines are met
  • Facilitation of site budgets and contract negotiations
  • Effective and open communication within the project team
  • Delivering onsite training of investigators and staff
  • Preparation and delivering of presentations at Investigator's Meetings
  • Preparation for and attendance at company's audits; resolution of audit findings
  • Support to global Regulatory Affairs in procurement of site regulatory documents
  • Maintenance of appropriate documentation regarding clinical site management
  • Participation in feasibility research
  • Participation in query resolution
  • Maintenance of study-specific automated tracking systems
Qualifications:
  • University degree in Life Sciences, Pharmacy, MD or RN or an equivalent combination of education, training and experience
  • At least 3 years of experience at a similar position, with full scope of monitoring responsibilities within Phase I-IV Clinical Trials
  • Independent monitoring experience in Australia
  • Experience in regulatory submissions, contract negotiations, site management and feasibility assessment
  • Fluent English, spoken and written
  • Team oriented with excellent communication and interpersonal skills including a positive and professional attitude to tasks and projects
  • Attention to detail, organizational and time-management skills
  • Demonstrated ability to multitask and work proactively in a fast-paced environment
  • Good problem solving abilities, flexibility
  • Ability to travel 
  • Demonstrated computer skills (MS Office applications)
  • Full working rights in Australia
Please get in touch for more information.