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Job Details

Associate Director Clinical Scientist

Company: Barrington James Clinical
Location:
Reference: jharvey
Closing Date: 23 Dec 17
Type: Full Time
Salary (£): Competitive
Benefits:

Job Summary:

Associate Director Clinical Scientist required for one of the most up and coming small global oncology sponsor companies in the US and EU.

Requirements:

Role: Associate Director Clinical Scientist (Oncology)

Location: New Jersey

 

My client, a small global Oncology sponsor company are looking for an Associate Director Clinical Scientist to join their team. They are not only located in the US but have offices globally across Europe. This role as the Associate Director Clinical Scientist would be an office based opportunity with flexibility and this is a chance to be part of a pivotal part of the company's growth for this year.

 

What makes this client stand out over your current role is that it is an opportunity to work on the ground level with a biotech company. This is an opportunity to work in the most desired and attractive area in the Life Sciences Industry. My client are about to take the market by storm with 8 products and 4 entering the early phase pipeline. They offer less red tape than other companies and a chance to put your own stamp on the development of the clinical trials. The right candidate will work on early phase Oncology trials and help the company not only grow but also themselves personally as this will be a hands on role. The AD Clinical Scientist will work closely with the Clinical Ops Team as well as the medical monitors on the following: 

 

Role expectations and Requirements:

  • Develop and maintain the study documents (protocol, consent template, IB, etc.)
  • Assist in writing the reports done annually, integrated medical reports, responses to regulatory authorities and boards, and other documents requiring data summarization
  • Serve as primary clinical liaison with biostatistics/data management team to ensure CRFs are appropriately designed
  • Perform the data review ongoing there, including data from vendors, AE/SAE reconciliation, etc.  
  • Follow up the key data findings to ensure resolution
  • Perform the pharmacovigilance data review and analysis, including participation in safety review team meetings
  • Develop and/or conduct training for study protocols, e.g. on the oncology disease area or therapeutic compounds
  • Provide the scientific oversight of vendors
  • Participate in scientific advisory boards; prepare and present clinical data at meetings externally 
  • Collaborate with the Clinical Operations to identify, engage, and train potential investigators, including participation in study site visits as needed
  • Review/develop the data review plans, statistical analysis plans, data output formats, etc.
  • Author and/or review clinical research SOPs
  • Support the clinical program leaders regarding ad-hoc requests from upper management

Qualifications

  • BS/BA degree in biological sciences or similar field
  • Minimum of 8-10 years of experience in the bio-pharmaceutical industry or other relevant clinical research experience, preferably in oncology
  • Working knowledge of ICH GCPs and other relevant regulatory/health authority experience
  • Strong writing and analytic skills, ideally with experience writing/presenting clinical documents and summarizing data
  • Experience with interacting with clinical investigators and medical experts.
  • Experience in working with CROs, including vendor selection, contract negotiation, managing CRO during clinical trial setup and conduct is preferrred
  • Demonstrated ability to work independently, exercise sound judgment, and adapt to changing work environment(s)
  • Excellent verbal, written, and interpersonal communication skills
  • Ability to travel up to 20%

If you think you have matched the required skill set of the expectations and requirements above then do not hesitate to apply. This is the chance to really join and get yourself in with a global company and grow with a organization that has ambitious and solid plans for growth in 2017.

If you are tired of being in a larger organization or not feeling fulfilled in your current role then do NOT miss out!

 

In order to apply, please contact Jack Harvey at 646 415 8221

 

**Interviews are STARTING ASAP**

Apply for this job: Associate Director Clinical Scientist

Contact Information:

Address:  Head Office
Victoria House Consort Way Horley Surrey
RH6 7AF
England
Tel:  01293 776644
Fax:  01293 822333
Website:  Visit Our Web Site

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