Market Research & Patient Support Programs (MAP) PV Scientist

Job description

  Job facts

With responsibility for Pharmacovigilance (PV) compliance of Market Research and Patient Support Programs (MAP), you'll ensure MAPs are conducted in compliance with global and local regulations and procedures. Partnering with Operations Vendor Management, you will oversee and support the activities performed by vendor (TCS) staff for MAP related PV activities including PV Approval of the MAPs, case transmission verification (CTV), source data quality check (SDQC) and case collection. Oversight, education and training of Service Providers conducting MAPs on Roche's behalf will also form part of your role as well as ensuring all dedicated systems and tools on which the process rely are effectively maintained and updated. You will act as deputy to the MAP PV Responsible during his/her absence and will partner with the Roche commercial function in the field of the MAP safety.

Your expertise and commitment will be instrumental in achieving excellent levels of program compliance. You'll represent PDS Operations at forums and carry out discussions with service providers, communicating accountabilities, deliverables and results.

Establishing monitoring, audit and inspection readiness activities in order to effectively gather and collect information, you'll develop processes and metrics which allow the identification of improvement opportunities and thorough assessment of operational processes. You'll collaborate with functional teams in determining processes and completion of agreed CAPA activities and develop methods for ensuring consistent delivery of processes across operations sites.

·  Who we are

Our UK Pharmaceutical head office is situated in Welwyn garden City, Hertfordshire, with beautiful country side surrounding the area. Supported by major motorways & airports as well as being a 30 minute train ride to London, access is easy. With over 1400 people occupying our site in Welwyn, you can expect opportunities in Early Development (pRED), Product Development (PD), Commercial (Rx) and of course our corporate function.

Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.

Desired profile

Who you are

You're someone who wants to influence your own development. You're looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.

With a degree in the field of healthcare or life sciences or an equivalent, you'll bring experience of working in a pharmaceutical safety role, experienced in working in an operational capacity and applying pharmacovigilance regulatory guidelines in practical scenarios. An effective team player who is confident in communicating and building relationships, you'll be skilled in leading projects to conclusion through good decision making and problem solving. You like to work in a global environment with cross-functional responsibilities.

In return we offer a competitive salary plus the excellent benefits you would expect from a bluechip organisation, including a genuine interest in your development.

Closing date: 6 September 2016

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