i-Pharm Consulting

Clinical Trial Manager – Home based - USA

North Carolina
13 Aug 2018
28 Jan 2019
Contract Type
The Client:

Our client is a successful vendor of choice for many Pharma and Biotech clients. They have an excellent reputation in the industry for giving employees a wealth of experience and opportunities internally. They have been involved in several ground-breaking discoveries over the last number of years and continue to work with exciting clients.

We have placed several other candidates in similar roles globally for this client. Feedback has always been very positive and their role openings are very sought after.

What Therapy Areas will you work within?

This position is available in the following teams with our client:

* Cardiovascular
* Oncology
* Internal Medicine
* General Medicine

Role Responsibilities and Scope:

* Management of Global Phase II/ III studies within various Indications of one of the above Therapeutic Areas from a clinical perspective
* The trials are globally based but your area of responsibility will be the US
* Site involvement at a level with CRAs when issues arise
* Forecast and manage budget and resource allocation within operational objectives
* Hold financial responsibility, tracking costs and profits
* Liaise with senior counterparts across the business to contribute to international departmental strategy
* Provide support to commercial teams, contributing to proposal and marketing material
* Lead by example, mentor and manage staff

To be suitable for this role you will:

* Several years’ experience in Clinical Research
* Excellent understanding of the principles of clinical study management
* Good clinical knowledge with an understanding of medical terminology
* Previous experience working within phases II / III for the Therapeutic Area you wish to work in
* At least 12 months experience in hands-on management of trials from a clinical stand point
* Ability to work independently
* Experience working in an international team environment under time and resource pressures.
* Excellent oral and written communication
* Proven leadership experience of integrated teams


Home based in the US with 20% travel for kick off meetings, investigator meetings


Competitive salary + benefits package on offer


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK, APAC, Europe and North America. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.



If you would like to discuss this vacancy further, please call Aoife on +1 347 967 5935 or email acronin@i-pharmconsulting.com. If this role is not suitable, Aoife is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


Permanent / Clinical Research / Clinical Study Manager / Clinical Trial Manager / Project Manager / Clinical Project Manager / CPM/ CSM / Clinical Operations / Biotech / Biopharma / Research / Niche Pharma / Boutique Pharma / Gene Therapy/ Rare Diseases / Medical / Oncology / Cardio / CNS / Cambridge / Boston / North East / Massachusetts / East Coast / America / New Jersey / New York / Connecticut / USA / i-Pharm New York / NYC / New York City / Alabama / Alaska / Arizona / Arkansas / California / Colorado / Connecticut / Delaware / Florida / Georgia / Hawaii / Idaho / Illinois / Indiana / Iowa / Kansas / Kentucky / Louisiana / Maine / Maryland / Massachusetts / Michigan / Minnesota / Mississippi / Missouri / Wyoming / Wisconsin / West Virginia / Washington / Virginia / Utah / Texas / Tennessee / South Dakota / South Carolina / Rhode Island / Pennsylvania / Oregon / Oklahoma / Ohio / North Dakota / North Carolina / New York / New Mexico / New Jersey / New Hampshire / Nevada / Nebraska / Montana

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