Clinical Senior Analyst

Location
Cambridge
Salary
£0 per annum
Posted
06 Jul 2017
Closes
03 Aug 2017
Ref
J3942
Contact
William Blohm
Contract Type
Permanent
Hours
Full Time
Job Description:

We are currently looking for a Clinical IS Senior Analyst to join a leading company based in the Cambridge area. As the Clinical IS Senior Analyst you will be a business partner to the Clinical Development groups. Focused on gaining an in depth understanding of business partner processes across Clinical, Quality, Pharmacovigilance, Regulatory, Data Management and related functions; they create strong collaborative relationships and take a leading role in the selection, design, implementation, validation, delivery and adoption of new information systems.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Clinical IS Senior Analyst will be varied however the key duties and responsibilities are as follows:

- Develops close working relationships with the Clinical Development teams through effective project engagement and consistent delivery of business expectations.
- Delivers high-value systems aligned with business requirements, collaborating closely during system selection, design, implementation, validation, and rollout to production.
- Works closely with business partners and stakeholders to ensure systems meet regulatory requirements utilising a risk-based approach to system validation.
- Supports effective adoption of new systems by working closely with business partners to create high-quality training materials and user support.
- Gains a detailed knowledge of Clinical Development business processes through shadowing, process review, and collaboration.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Clinical IS Senior Analyst we are looking to identify the following on your profile and past history:

- Demonstrable experience overseeing the planning, delivery and maintenance of a portfolio of business critical computerised solutions on time and on budget.
- Working knowledge of the system design lifecycle, IT project management and development of validation/qualification documentation within a regulated environment.
- Interfacing and collaborating with both technical and non-technical colleagues including IT contractors/developers, business stakeholders and customers, vendors/suppliers, at all levels including senior management and board level.
- Strong decision making skills, able to develop positive coaching/mentoring relationships with matrixed team members.
- Excellent analytical and problem solving skills. Able to understand and absorb complex information and requirements.
- Excellent organisational skills, meticulous and methodical. Good at prioritising and flexible enough to adapt plans. Comfortable working to tight deadlines and within constraints.
- Excellent written and verbal communication skills, strong presentation skills, and able to communicate complex information in simple terms.
- Ability to develop pragmatic, innovative approaches to the adoption of technology/IS solutions within strict regulatory constraints.
- Forms trusting, collaborative and strategic relationships with internal stakeholders and external partners with skills in assertion, negotiation, influencing, tact and diplomacy.
- Can instil a culture of considered change management for his or her deliverables in order to drive effective adoption and maximise the customer experience.
- Has a Service' mentality, recognising and promoting the enabling value that technology can provide to customers.

Key Words: Clinical, Quality, Pharmacovigilance, Regulatory, Data Management, system selection, design, implementation, validation, analytical

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