Requisition Number: 8337
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 3,500+ 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 Medical Affairs does at Worldwide
Medical Affairs plays a pivotal role throughout the entire life cycle of a clinical investigation, exerting its influence from the initial stages of Business Development to the final Regulatory Submissions. Within this multifaceted domain, the dedicated members of the Medical Affairs team provide essential support to the broader project team, contributing to the cultivation of the scientific and medical principles that define Worldwide's philosophy.
What you will do
Tasks may include but are not limited to:
- Serves as Global Lead Medical Monitor (GLMM) for pan-regional and/or global trial(s) to which s/he is assigned, providing 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.
- 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, review of relevant therapeutic/clinical literature, and attendance in conferences and meetings.
- Assists in the annual attainment of departmental revenue targets and any other activities as directed by senior management.
What you will bring to the role
- Experience reviewing and/or assisting in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs, etc.) as directed by senior management.
- Proven track record of independently supporting 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.
- Exhibits the necessary skillset to mentor 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.
- Robust clinical/therapeutic acumen in medical subspecialty.
- Working knowledge of GCPs and regulatory requirements relating to clinical development and safety to assure compliance with ethical, legal and regulatory standards.
Your experience
- Medical Degree from an accredited institution of Medical Education.
- Experience in Obesity, T2DM and T1D.
- 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.
We love knowing that someone is going to have a better life because of the work we do.
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