15 Oct

Senior Scientific Associate Jobs Vacancy in Charles River Laboratories Horsham

Position
Senior Scientific Associate
Company
Charles River Laboratories
Location
Horsham Papua
Opening
15 Oct, 2018 30+ days ago

Charles River Laboratories Horsham urgently required following position for Senior Scientific Associate. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.

Follow the online directions, complete all the necessary fields, and provide all relevant information so your application is submitted correctly. When you click the 'Apply this Job' button (open in new window) you will be taken to the online application form. Here you will be asked to provide personal and contact details, respond to employment-related questions, and show how you meet the key selection criteria.

Senior Scientific Associate Jobs Vacancy in Charles River Laboratories Horsham Jobs Details:

For 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.



Job Summary


Responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies assigned by TFM within safety assessment. Responsible for protocols/study plans, coordinate with technical teams to allow appropriate execution of the study, including establishing study schedules, ensuring adequate Standard Operating Procedures are available and adhered to, oversees adequate data recording and reporting, and ensure regulatory requirements/expectations are met for the assigned study(ies). Overall interpretation of preclinical toxicity studies, evaluation and preparation of reports from the data collected during these studies, communication with sponsor representatives, initiating contact with potential clients will be required, Familiarity with study costs and impact of changes will be required. May be involved with development of new technologies/procedures.


ESSENTIAL DUTIES AND RESPONSIBILITIES:

  • Function as an independent Study Director in accordance with the applicable Good Laboratory Practices (GLPs).
    • Designs, writes, reviews and edits, as necessary, Study Plans, amendments and study schedules that define and schedule all study activities.
    • Oversees and coordinates all aspects of study procedures, whether performed within the department or by service departments.
    • Ensures that projects are performed according to Standard Operating Procedures and Good Laboratory Practice regulations and is aware of appropriate regulations, guidelines and guidances.
    • Writes, reviews and edits, as necessary, draft or final reports that document all study related procedures and results.
    • Prompt verbal or written communication with Sponsors on study related business.

  • Understands regulations and GLP’s as they relate to primary area of focus.
  • Understands the study process from proposal to report.
  • Oversees and coordinates study conduct (protocol development, technical guidance, and reporting).
  • Assists in study planning, scheduling, and execution under the supervision of Sr. Scientist(s)/Scientific Manager.
  • Host client visits and telephone/video conferences with support/guidance from Sr. Scientist(s) as needed.
  • Effectively communicates with internal and external clients in a manner that generates confidence and builds trust.
  • Works on studies/programs of basic complexity.
  • Basic knowledge of Quality Assurance (QA)/Quality Control (QC) process
  • Interacts with veterinary staff, understands the IACUC process, and understands the Study Director role in animal welfare.
  • Gains familiarity with overall project costs and communicates with the technical supervisor as well as the Scientific Manager on issues of staffing and equipment.
  • May attend scientific meetings, conferences and training courses to enhance job and professional skills.


QUALIFICATIONS:

  • Education: Minimum of a Bachelor’s degree (BA/BS) or equivalent in Toxicology, Pharmacology, or related discipline. Prefer Master’s (MA/MS), Doctorate (PhD), PharmD, DVM, or MD degree or equivalent.
  • Experience: No work experience required.
  • An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.




About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 120 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.


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