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
View more
- Discipline
- Medical Affairs
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
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
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
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.
- Website
- https://www.worldwide.com/
- 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
Get job alerts
Create a job alert and receive personalised job recommendations straight to your inbox.
Create alert