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Medical Director Hematology (Haematologist) - Office Based Excellent Salary, Car and Bonus

Employer
Barrington James
Location
Reading, Berkshire (GB)
Salary
Highly Competitive, Car and Bonus
Start date
17 Apr 2019
Closing date
17 May 2019

Job Details

This position offers:

Work for a Leading CRO on Hematology / Oncology Trials

Excellent basic plus car and bonus

Career progression to Senior Medical Director

Job security and stability in a consistently growing CRO

 

 

Medical Director, you will provide therapeutic expertise and to the external customers. You will use your therapeutic knowledge to help build on the foundations of our existing business (BD).  Key responsibilities in this challenging and highly varied role consist of medical study monitoring, including (but not limited to) the review of trial protocols, providing medical and scientific support to the clinical teams and investigation sites, medical review of clinical laboratory results, and input to final study reports.  An excellent communicator, and ideally have “commercial” skills within marketing and sales.

Participate in all aspects of Medical/Scientific Services' involvement on assigned trials. Offer leadership, management and direction to assigned staff. Assists in the implementation of department mission, goals and objectives, oversight of operations, development of policies and procedures and standards for the department.

RESPONSIBILITIES
• Serves as Regional Medical Advisor on assigned projects.
• Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
• Performs review and clarification of trial-related Adverse Events (AEs).
• Performs medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative.
• Provides medical support for the Analysis Of Similar Events (AOSE).
• Performs medical review of Adverse Event coding.
• Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
• Performs review of the Clinical Study Report (CSR) and patient narratives.
• Available 24 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites.
• Attends and presents at Investigator Meetings.
• Provides therapeutic area/indication training for the project clinical team.
• Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
• Serves as Scientific Advisor and provides guidance to Project Managers on the medical and scientific aspects of assigned projects.
• Provides support to the proposal development team which may include, but is not limited to, reviewing the protocol for feasibility, giving guidance as to anticipated enrollment, and general advice as to the various risks associated with running a particular study.
• Participates in development of Medical and Scientific Services portion of client proposals including the budgeting process.
• Serves as a resource, and may participate in strategic business development activities including presentations to prospective clients, professional meetings, and other business development activities for Medical & Scientific Services.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Ability to establish and meet priorities, deadlines, strategic department goals and objectives.
• Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility.
• Ability to establish and maintain effective working relationships with co-workers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE
• A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education, along with a medical license, or equivalent, from the country or region in which he/she resides and works is required, plus experience in clinical medicine, in addition to clinical trials experience as an investigator or in the Pharma, CRO, or Biotech industry. Specialty Board certification required; or equivalent combination of education, training and experience

Want to find out more and APPLY NOW?

This opportunity has understandably been incredibly popular. We encourage all interested candidates to apply without delay as it is likely that recruitment will close prematurely. Please direct all questions (if necessary) to “Chris” at cswain (at) barringtonjames (dot) com alongside a copy of your CV.

Company

We’re great at what we do. A collection of the worlds finest Life Science recruiters working for the worlds best Life Science consultancy.

Originally, a purely contingency and contract recruiter, focused in the UK, Barrington James is now a sophisticated, highly effective provider of human resources solutions up to full RPO, partnering the pharma, medical devices, and healthcare industries right across the globe.

Company info
Website
Telephone
01293 776644
Location
Victoria House
Consort Way
Horley
Surrey
RH6 7AF
GB

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