Simbec Orion Group Ltd

Oncology Associate Medical Director

Location
New York, United States
Salary
Competitive
Posted
12 Feb 2021
Closes
14 Mar 2021
Ref
VA106
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Simbec-Orion is a responsive and agile full-service CRO, with wide therapeutic experience and specialist expertise in clinical pharmacology, oncology and rare diseases. Perfectly structured, we provide full-service clinical development solutions for small and mid-size drug developers - headed up by a centralised leadership team.

With a focus on tailormade and scalable solutions, we'll adapt our delivery style, communications and operations to suit the demands of your project, helping you achieve your clinical and commercial objectives. Because our goal is the same as yours; to improve patients' lives.

Main Duties and Responsibilities:

We are looking for an Oncology Associate Medical Director to join our Medical - Clinical Development department.

You will assume medical responsibility for clinical studies conducted by Simbec‑Orion and are responsible for the clinical interpretation of data to ensure clinical trials are conducted such that subjects' rights, safety and wellbeing are protected and that the clinical trial data is reliable. You will also assist in cross-departmental medical monitoring activities and work with the wider cross-functional team that includes Clinical Operations, Project Management, Pharmacovigilance, Business Development, Biometrics and Regulatory and Technical Writing.

Minimum Requirements:

Essential:
  • Medical Degree
  • Previous experience working in a field of Oncology
  • Experience in medical monitoring, review of patient, laboratory, and safety within a clinical research environment
  • Experience in business development activities including feasibility and strategic advice for proposal development and bid-defence meetings
  • Excellent organization and time management skills.
  • Ability to effectively manage any changes to priorities/deadlines
  • Professional communication and presentation skills
  • Strong computer skills including but not limited to the knowledge of electronic data capturing systems and MS-Office products such as Excel and Word

Desirable:
  • GMC Registered with a License to Practice
  • Post-graduate Qualification in Clinical Pharmacology / Pharmaceutical Medicine
  • Pharmacovigilance experience
  • Previous experience of working within a CRO, biotech or pharmaceutical company


Simbec-Orion is an equal opportunity employer. Simbec-Orion will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law.