Associate Medical Director, Medical Affairs

4 months ago

United Kingdom Worldwide Clinical Trials Full time

**Requisition Number**7731**

**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 fast-paced 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 four-year 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

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