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Clinical Study Manager - Home Based

Clinical Study Manager - Home Based

Job Title: Clinical Study Manager - Home Based
Contract Type: Contract
Location: Home Based
Industry:
Salary: £ Competitive
Start Date: ASAP
Reference: 15857 BT
Contact Name: Brian Tappy
Contact Email: brian.tappy@nextphaserecruitment.com
Job Published: May 03, 2018 10:58

Job Description

To be home based in the UK with a flexible working hours contract, are you a Clinical Study Manager with extensive global trial leadership experience in Oncology studies? Would you consider a challenging long-term contract with an innovator in the Oncology field leading a team passionate about their work? Are you looking to form a long-term relationship with an organisation that engages contractors in strategic roles? If the answer to each of these questions is YES then please do read on…………

The Company

The company is a highly successful pharmaceutical company that is expanding through exceeding performance targets. The organisation has a high investment ratio in drug development with a record number of compounds in clinical studies and more planned. Oncology is a strategic therapeutic area where the company has further clinical trial funding as it continues to enhance its position as a pioneer and innovator in this field.  

The Role

The focus of this role is study ownership and study team leadership of an Oncology study that will be running in multiple countries (Europe and Asia Pacific at least) dependent on patient availability. The study will be complex in nature and involves an emphasis on aspects such as patient recruitment strategy and data quality plus overall leadership abilities.

The Study Manager is responsible for all aspects of the assigned study from conception to final medical report including the budget and measurable deliverables. The responsibilities encompass all aspects of the planning, implementation, analysis and reporting of the study within the timelines and budgets. An important element is the identification and management of a cross-functional international team. There will be an initial focus on patient recruitment strategy and ongoing emphasis on quality of data.

A full job specification is available on request.

The Contract

The contract is for an initial 12 months which will extendable by 12-month periods. The expectation is to work with the company for the duration of the study phase as a minimum however they look to secure long term relationships with contractors. The company is highly “contractor friendly” with a significant proportion of clinical management staff being “in-sourced colleagues”. The contract provides the security of a 2-month notice period with a competitive daily rate and flexible 7 hour working day.

We can accommodate notice periods with a flexible start date; securing the right candidate is of prime importance. 

Experience

We are seeking a committed individual with global clinical trial management and leadership experience in Oncology studies. Due to the international nature of the studies and study team you will need to demonstrate a strong appreciation of working with a variety of cultures. Candidates will be considered from pharmaceutical, bio-tech, CRO and not-for-profit environments.