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Medical Director, Gen Med/Rare Disease, EU (Remote)

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

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

Job Details

SUMMARY:
 
To provide medical management and professional medical support for clinical research projects at WORLDWIDE as the assigned Medical Monitor (MM). To assist in activities requiring Medical 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.    

LOCATION: This role can be home based anywhere in Europe.

 
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 teams 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
  • As directed 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  assure compliance with ethical, legal and regulatory standards
  • Assists in the mentoring of other medical staff) as directed by Senior management and by consistently displaying exemplary work ethics, compassion and integrity, supports Senior Management's leadership of both the department and the company
  • Maintains clinical/therapeutic acumen in medical subspecialty through online and/or in person scholarly programs/lectures
  • Demonstrates competence  with the execution of  SAE related medical review in WORLDWIDEs 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.
 

OTHER SKILLS AND ABILITIES:
 
  • Excellent computer skills (Word, Excel, Access)
  • Excellent spoken and written English skills
  • Excellent organizational and time management skills
  • Excellent communication skills
  • Excellent presentation skills
 
 
REQUIREMENTS:
 
  • Medical Degree from an accredited institution of Medical Education.
  • At least 2  years of medical monitoring in clinical research or related industry
  • Valid passport and ability to travel as required.
   
Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.

#LI-EW1
#CRO
#REMOTE
#RAREDISEASE
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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