Associate Medical Director, Medical Affairs - United Kingdom - Worldwide Clinical Trials

Worldwide Clinical Trials

Verified Company

United Kingdom

2 weeks ago

Posted by:

Tom O´Connor

beBee Recruiter

Description

Requisition Number7731**
Employment Type:Regular**
Who we are

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality.

Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.

Our talented team of 3,000+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers.

From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed.

We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity.

We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Join us

What an Associate Medical Director does at Worldwide

To provide support for clinical research projects at Worldwide as assigned by head of the Medical Affairs function or respective Therapeutic Medical Lead(s).

Management of electronic systems applicable to Medical Affairs. Support in medical data review, management and reporting.

What you will do

As directed by Medical Affairs management or Therapeutic Medical Leads provides initial review, compilation and reporting of study data.
Provide operational support to Medical Affairs function.
Prepares meeting agendas, manages functional project review documentation, develops and manages study documents pertaining to Medical Affairs, takes minutes for respective meetings.
Responsible for updating the functional documents repository.
Assists Medical Affairs management with internal budget management, tracking and forecasting
Assists with verification of contracted services as directed by Medical Affairs function head or Therapeutic Medical Lead(s)

What you will bring to the role

Excellent written and verbal communication skills
Ability to work independently and as a team member
Strong interpersonal skills in a fastpaced and rapidly changing environment
Ability to exercise independent judgment with sensitivity to decisions requiring supervisory approval
Ability to handle multiple tasks, including rapid response in generating new documents, forms and tools
Strong organizational skills
Knowledge and understanding of ICH, GCP and FDA or EU directive regulations (as applicable) as well as local regulatory requirements Excellent spoken and written English skills
Your experience
A minimum fouryear college curriculum with a major concentration in medical, biological, physical, health, pharmacy or other related science and minimum 5 years of industry experience or
MD degree with a minimum of 1 year of industry experience
Ideally will have had relevant experience in clinical management or project management roles.

Why Worldwide
We love knowing that someone is going to have a better life because of the work we do.

LI-FD1

LI-remote