Medical Science Liaison, Oncology

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GreenLight Clinical is seeking an experienced and proactive Medical Science Liaison, Oncology to join the team.

Summary about this job

Pharmaceuticals & Medical Devices

Company: GreenLight Clinical

Location: Sydney

Work type: Full Time

Salary: n\a

Phone: +61-7-4258-1711

Fax: +61-2-3964-8882

E-mail: n\a

Site:

Detail information about job Medical Science Liaison, Oncology. Terms and conditions vacancy

  • Full service Contract Research Organisation (CRO)
  • Collegial and collaborative in a fast-growing organisation working environment
  • Sydney-based with regular travel within Australia/Overseas

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 an experienced, highly motivated and enthusiastic Medical Science Liaison, to be the Oncology scientific expert responsible for all preclinical activities, driving the pipeline forward and ensuring clinical development and implementation.  

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

  • Development of partnerships with investigators, opinion leaders, healthcare professionals and sponsors
  • Scientific evidence-based advisor and communicator to both internal (clinical, data management, business development, statistical and marketing teams) and external stakeholders
  • Input and active participation with medical educational programmes, advisory boards and therapeutic area training.
  • Active participation in clinical trial operational activities such as study feasibilities and RA/HREC submissions
  • Planning, design and development of Protocol synopsis, Protocols, Investigator Brochures, Manual Of Procedures, Patient Informed Consent Forms and other essentials documents
  • Development, implementation and management of preclinical activities

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

Essential

  • BSc (Hons) and significant medical/clinical experience in Oncology
  • The ability to understand, process, communicate and present scientific information to a high standard
  • External customer focus with strong networking capabilities and integration with KOLs
  • Excellent influencing, networking, presentation and communication skills and a proven track record of team cross-functional team working
  • Ability to manage multiple projects and adapt priorities according to business and strategic needs, in a entrepreneurial, fast-paced environment
  • Ability to travel locally or internationally

Desirable

  • PhD, MB BS, MB ChB
  • Minimum 2 years pharmaceutical/CRO industry experience is preferable.


Would you like to know more?

If you want to know more about the position including a copy of the job description, you are welcome to contact [email protected] We look forward to hearing from you.

 

About Applying

To apply for this role, please send your application to [email protected]  by 5.00pm AEST 13 July 2018.

*Applications must specify residency or work visa status, include a CV and a Cover Letter which includes responses to the role requirements (Selection Criteria) detailed above.


Greenlight Clinical is an EEO employer and values diversity. We encourage applications from women, Aboriginal and Torres Strait Islanders, people with disability, LGBTIQ individuals and applicants of diverse cultures 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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