Senior Clinical Site Manager

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GreenLight Clinical is seeking an experienced and proactive Senior Clinical Site Manager

Summary about this job

Clinical/Medical Research

Company: GreenLight Clinical

Location: Sydney

Work type: Full Time

Salary: n\a

Phone: +61-8-2001-9089

Fax: +61-2-4654-7807

E-mail: n\a

Site:

Detail information about job Senior Clinical Site Manager. Terms and conditions vacancy

  • Customer-Focused Full service Contract Research Organisation (CRO)
  • Collegial and Collaborative Working Environment
  • Full time , 12 months contract role, based in Sydney office

About Us
Greenlight Clinical is a full-service Contract Research Organisation (CRO) that addresses the clinical trial needs of both local and international pharmaceutical, biotechnology and medical device companies. Our dedicated team offers clients the unrivalled expertise of Investigators who have managed clinical studies and enrolled thousands of patients onto Phase I, II and III studies used for drug and device registration around the world.

We are currently seeking a highly experienced and collaborative Senior Clinical Site Manager/Project Manager to be responsible for the implementation and conduct of global or local Phase 1 - 4 clinical studies.


About the Role
Reporting to the Chief Scientific Officer / Head of Clinical Operations, this role’s responsibilities include but are not limited to:

  • Project management of assigned activities as assigned at the discretion of the Chief Scientific Officer and Head of Clinical Operations
  • Monitor clinical studies (remote, onsite or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations. Manage Investigative Sites remotely between visits via telephone calls and other channels of communication.
  • Mentoring and co-monitoring visits with junior, or new, clinical team members
  • Plan day to day activities for monitoring of a clinical study and ensure the accurate and timely submission of Monitoring Reports
  • Prepare and conduct on-site qualification, study initiation, interim monitoring and close-out monitoring visits at investigator sites

 

About You
In order to be considered for this role, you will possess the following role requirements (Selection Criteria):

Essential

  • Undergraduate degree or its international equivalent in clinical science or health-related field from an accredited institution
  • At least 3 years local experience in monitoring clinical trials with a Pharmaceutical or CRO background
  • Solid understanding of ICH / GCP regulations
  • Willingness to travel and a valid drivers licence and passport
  • Self- starter with ability to adapt and be flexible to changing priorities
  • Comfortable with broad responsibilities in an entrepreneurial, fast-paced company environment

We offer

  • Opportunity to be part of a growing organisation
  • An organisation that values their staff
  • Committed and hardworking team to work with
  • Rewarding opportunity to make a difference

Would you like to know more?

To learn more about GreenLight Clinical please visit our website on http://www.greenlightclinical.com/ and to obtain a copy of the job description which details more of the role accountabilities, you are welcome to contact [email protected]  

About Applying

To apply for this role, please send your application to [email protected]  by 5.00pm AEST 20 July 2018.

*Applications must specify residency or work visa status, include your CV and a Cover Letter which includes responses to the Selection Criteria detailed in the position description.


Greenlight Clinical is an EEO employer and values diversity. We encourage applications from people of diverse cultures, gender and ages.

The personal data collected will be used for recruitment purposes only. We reserve the right to conduct police checks and other screening procedures prior to employment being confirmed.

 

 

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