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Senior Medical Director, Oncology, EU, (REMOTE)

Employer
Worldwide Clinical Trials
Location
HOMEWORKING, Nottingham, United Kingdom
Salary
Competitive
Start date
16 Oct 2019
Closing date
15 Nov 2019

View more

Discipline
Medical Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

The Medical Affairs team at Worldwide Clinical Trials is hiring a Senior Medical Director, Medical Monitor, ONCOLOGY, EU (REMOTE)

We're Worldwide Clinical Trials, the Uncommon CRO. Founded by physicians dedicated to advancing medical science and built on an unwavering commitment to operational excellence, we strategically balance science, medicine, operations, and commercial intelligence to achieve successful drug development. Combining therapeutic expertise - most notably in Neuroscience, Cardiovascular, Immune-Mediated Inflammatory Disorders, Oncology and Rare Disease - with proactive insights and rigorous operations, we successfully manage clinical trials across more than 60 countries.

ROLE:
To provide medical management and professional medical support for clinical research projects at Worldwide Clinical Trials as the assigned Medical Monitor (MM).  To assist in activities requiring Medical & Scientific support, including but not limited to:  assistance with feasibility assessments, medical training and provision of medical/clinical input to the design of study protocols and/or clinical development programs as well as assistance with business development activities, as directed by the department head.

RESPONSIBILITIES:
Tasks may include but are not limited to:
  • Medically manages clinical trials to which s/he is assigned as MM
  • Serves as Global Lead MM (GLMM) for pan-regional and/or global trial(s) to which s/he is assigned
  • Collaborates with the other members of the Medical & Safety project team to process Serious Adverse Events (SAEs)
  • Provides therapeutic and protocol-specific training to the project teams
  • Contributes medical input into the design of clinical development programs, study protocols, research papers, client focused white papers, etc.
  • Provides after hours medical support for projects to which s/he is assigned
  • Independently supports Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management
  • Reviews and/or assist in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs etc.,) as directed by senior management
  • Maintains a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings (company-wide project tracking, medical management meeting, etc.) , review of relevant therapeutic/clinical literature and attendance in conferences and meetings
  • Interacts with staff in other functional areas within the company to ensure the highest level of client satisfaction through successful execution of projects
  • Identifies, documents and appropriately resolves out-of-scope work as directed by senior management
  • Assists in the annual attainment of departmental revenue targets and any other activities as directed by senior management 
  • Maintains working knowledge of GCPs and regulatory requirements relating to clinical development and safety and assure compliance with ethical, legal and regulatory standards
  • Mentors other medical staff as directed by Senior management and by consistently displaying exemplary work ethics, compassion and integrity, support Senior Management's leadership of both the department and the company
  • Maintains clinical/therapeutic acumen in medical sub-specialty through online and/or in person scholarly programs/lectures
  • Demonstrates competence with the execution of SAE related medical review in Worldwide's electronic safety database
  • Perform other duties as assigned.  The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
     
REQUIREMENTS: 
  • Medical Degree from an accredited institution of Medical Education.
  • 6-8 years in the CRO, Pharma or Biotech industry with the medical monitoring or study physician role.
  • Valid passport and ability to travel if required.
#uncommoncro
#LI-EW1
#REMOTE
 
Description Key Responsibilities Benefits

Company

Find out more about working for our company

Worldwide Clinical Trials -hub-button

Brief Company Description; 

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

 

Company info
Website
Mini-site
Worldwide Clinical Trials
Telephone
+44 115 956 7711
Location
1st Floor Waterfront House
Beeston Business Park
Beeston
Nottingham
Nottinghamshire
NG9 1LA
United Kingdom

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