i-Pharm Consulting

Clinical Project Management Director – Immunology / Oncology

28 Nov 2018
12 Dec 2018
Clinical Research
Contract Type
Clinical Project Management Director – Immunology / Oncology – Late Phase

i-Pharm Consulting have partnered with a global Pharmaceutical company to source an experienced Clinical Project Management within Oncology or Immunology to join their Late Stage division.

This position is an excellent opportunity for an experienced Clinical Project Management professional to join a successful team and influence the future direction of various Immunology / Oncology based trials. In this role, you will act as a leading figure in supporting global clinical directors and trial design teams in finding and structuring clinical information driving optimal designs for late stage oncology drug development.

You will be part of a truly global team alongside some of the most respected statistical programming, information practice and analytics specialists in the industry. Your medical expertise, understanding and communication to the various Clinical Project team members is essential to future success of this division.


Office based - Maryland


Excellent salary & benefits package on offer

You will also lead key drug meetings and committees by establishing the scope, goals and deliverables supporting business goals in collaboration with senior management and decision makers. This will include developing and controlling deadlines as well as preparing progress reports.

The significant areas for contribution are:

* Influencing late stage drug development decisions by using data to support clinical trial design
* Using techniques such as: text mining, data visualization, competitor intelligence, and benchmarking extract key relevant information proactively enabling clinical drug design decision makers to make timely and objective decisions
* Lead the design team by collaborating with project stakeholders to plan and schedule project timelines tracking project landmarks
* Facilitate access to complex information for the drug project and ensure access to and (re)use of clinical information, documents and data


To be considered for this opportunity you will have demonstrable experience of late stage oncology drug development.

You will have a real passion for clinical data and information and proven insightful ability to know what information to seek, how to find it, and how to share it with the teams in a clear and meaningful way. You will be a creative thinker with an appetite for doing things differently.

You’ll be excited by the prospect of playing a lead role within late stage oncology drug development projects. An excellent communicator with great listening skills, who can absorb information and respond in a concise manner.

In addition, you will also have:

* Deep understanding of the late stage clinical drug development process in oncology, immuno-oncology or immunology
* Good understanding of project management techniques and methods
* Experience in clinical information or science information setting in the application of information and knowledge management
* Demonstrated leadership capability – including ability to influence stakeholders
* Good organizational skills and the ability to multitask; can set priorities and follow a timeline
* Great attention to detail
* Bachelors and/or advanced degree in a Life Science or related subject, +/- MBA, or equivalent relevant experience


Medical Information / Oncology / Late Phase / Late Stage / Immunology / Medical Affairs / Clinical Trial Management / Pharmaceutical / Biopharma / Clinical Management /Clinical trial Management / Clinical Project Director / MSL / Medical Science Liaison / Oncology / Immunology / Immuno-Oncology / Maryland / East Coast USA

Job Type: Full-time

Salary: $160,000.00 to $180,000.00 /year

Job Type: Full-time

Salary: $160,000.00 to $180,000.00 /year

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