join us

The strength of any organisation is in its people. This is particularly true of Cmed. We are seeking to fill the following positions.

Biostatistics
Clinical
Technology
Data Management

Biostatistics

Director/Global Head of Biostatistics

Geographical Location	Horsham, W. Sussex, UK
Contact Information	Sarah Thompson, sthompson@cmedresearch.com, +44 (0)1403 755050
Applications Before	30th September 2008
Remuneration	Competitive

About

Cmed is rapidly developing an industry leading reputation in the conduct analysis of Bayesian/ adaptive trial design and we are seeking a Senior statistician with both extensive Pharma and CRO experience to take this forward as Director/ Global Head of Biostatistics. You will be based in our Head Office in Horsham, West Sussex

We provide excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits.

Principal Duties and Responsibilities

Cmed provide a complete statistical service including statistical input to study design, protocol development, consultancy, planning, specifying and performing statistical analyses, conducting their write-up, and collaboration in the production of integrated study reports.

Your role will include:-

The recruitment and development of all staff, Statistics and SAS Programming infrastructure implementation and maintenance, resourcing the department to meet timelines and deliver on budget. You will also be responsible for the financial performance of the department, including forecasting and compliance with MIS processes.

Further, you would lead development of 'best-in-class' analysis and reporting processes to ensure operational efficiency of Cmed Biostatistics' function. You would also ensure the group works in partnership with other Cmed line units, processes and partners to include, but not be restricted to, DMO, HR, Finance and MIS.

Candidate Profile

You will have a BSc and/or an MSc in Statistics and significant relevant experience as a lead statistician and department manager of personnel in a CRO or pharmaceutical company. You will have a strong Statistical methodology background in Phase II to IV clinical trials. Previous experience of Oncology and Early Phase Trials will be an advantage, with at least 8 years experience in Biomedical Statistics or SAS Programming (statistical programming) within a CRO or pharmaceutical company. You should also possess excellent knowledge/experience in SAS Programming and have expertise in global clinical trial practices, procedures and methodolgies.

We are looking for dynamic, professionals with a depth of statistical understanding and associated clinical trials experience, as well as a sound knowledge of SAS. You will also need to be pro-active with a proven ability to work in multidisciplinary teams to agreed timelines, and most importantly, to be able to communicate effectively to both Statisticians and Non-Statisticians alike.

Senior Biostatistician, UK

Geographical Location	Horsham, W. Sussex, UK
Contact Information	Sarah Thompson, sthompson@cmedresearch.com, +44 (0)1403 755050
Applications Before	30th September 2008
Remuneration	Competitive

About

We are seeking ambitious individuals to join our growing Biostatistics group based in Horsham, West Sussex to contribute to our statistical design, analysis and reporting services. We provide excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits

Principal Duties and Responsibilities

You would be involved in all of the above areas, and would be responsible for statistical aspects of projects which could range in size from small early phase I trials to larger later phase II-IV trials across a comprehensive range of therapeutic areas. In the role you would provide input to study protocols, program and conduct statistical analyses providing high quality "report ready" statistical output and critically review results and conclusions to ensure their valid and correct interpretation.

Further, you would develop key documents including the Statistical Analysis Plan, Quality Control and Project Conventions Plans, and, working closely with our Statistical Programmers review the derived data set specifications and trial safety data tables, listings and figures they produce. You would also be responsible for providing the statistical input into parts of the Data Management process including reviewing the eCRF (or CRF), database structure and data cleaning strategies.

Candidate Profile

You will have a BSc and/or an MSc in Statistics and have at least 4 years relevant experience in the area of the design and analysis of clinical trials. Experience of the design and analysis of Oncology studies would be desirable although not essential.

Senior Statistical Programmer, UK

Geographical Location	Horsham, W. Sussex, UK
Contact Information	Sarah Thompson, sthompson@cmedresearch.com, +44 (0)1403 755050
Applications Before	30th September 2008
Remuneration	Competitive

About

Cmed are seeking experienced Statistical Programmers to join their growing Statistical Programming group based in Horsham, West Sussex.

We provide excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits

Principal Duties and Responsibilities

Cmed provide a complete statistical service to pharmaceutical and biotechnology companies. You would be responsible for the statistical programming deliverables of projects ranging from early phase I trials to larger phase II-IV trials across a comprehensive range of therapeutic areas. You would carry out the statistical programming for both the production and QC of derived data sets, data listings, data summaries, figures and statistical appendices for global Phase I-IV trials. Further, you would specify programming strategy, devise and implement project conventions and, working closely with our Biostatisticians, input into project QC plans.

Candidate Profile

We are looking for professionals with excellent SAS programming skills accompanied by an in depth understanding of clinical trial reporting processes. You will also need to be pro-active with a proven ability to work in multidisciplinary teams to agreed timelines, and most importantly, to be able to communicate effectively with people from other disciplines.

You will have a BSc/BA or equivalent in computer science, mathematics, statistics, life sciences or related field(s) and have at least 4 years relevant experience in reporting clinical trials data.

Clinical

Lead C R A

Geographical Location	Horsham, UK
Contact Information	recruitment @cmedresearch.com, 01403 755050
Applications Before	30 September 2008
Remuneration	Competitive

Principal Duties and Responsibilities

Line management of field based CRA's: Goal setting (with Clinical Project Manager), problem solving, pastoral care.
Present project specific training to study team.
Assist with site recruitment and start up activities.
Perform qualification, initiation, monitoring and close out visits as necessary.

Candidate Profile

3+ years of experience as a CRA within Pharma/CRO industry.

Technology

Software Test Engineer

Geographical Location	Horsham, W. Sussex, UK
Contact Information	Sarah Thompson, sthompson@cmedresearch.com, 01403 755050
Applications Before	30th September 2008
Remuneration	Competitive

About

We are seeking an experienced software tester to join our team based in Horsham, West Sussex, We provide excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits.

Principal Duties and Responsibilities

The Software Test team play a pivotal role in ensuring the consistent quality and timely delivery of our unique software, Timeaus. As a Software Test Engineer you will be working within a small team of other testers and along developers and end users.

Candidate Profile

This position would appeal to candidates with previous expereince of working as a Software Tester who have an intersting in working on a product provding cutting edge services within the Clinical Trials arena. The successful candidate will be degree qualified and have at least 2 years experience in a similar role.

Good communication skills are essential for all positions as well as the ability to work effectively in teams, a can do attitude and enthusiastic personality.

Data Management

Director of Data Management Operations

Geographical Location	New Providence, NJ, US
Contact Information	lburroughs@cmedresearch.com, +1 214 491 2909
Applications Before	31 Aug 2008
Remuneration	Competitive

About

Are you looking for an opportunity to have a direct impact on the success of a growing organization?
Would you like to have your achievements recognized by Senior Management?
Now imagine yourself working for a company that offers the opportunity to make a difference.
Now imagine yourself working for a company with an emphasis on work life balance.
Now imagine that same company can collect clinical trial data electronically in a remote African village without electricity or access to the internet.

Sound impossible?

At Cmed anything is possible.

Cmed is an eCRO, based in the US and Europe that uniquely combines a Clinical Research Organization and a state of the art technology development company. The operational activities of our CRO division are underpinned by Timaeus. We believe Timaeus is the world's most sophisticated and complete electronic data capture and management system that can work anywhere in the world there is mobile phone or satellite coverage.

Let us show you how we have captured the impossible.

Principal Duties and Responsibilities

As Director, Data Management Operations (US) you will:

Ensure that Cmed Inc. delivers quality data management service and projects to clients and achieves agreed upon revenue margins
Use your expertise to oversee the coordination of data management operations and project deliverables, ensuring project milestones are met according to agreed upon timelines with high quality
Be responsible for the continued growth, development and management of the U.S. Data Management Operations Team to ensure their performance meets/exceeds both the business and their own personal goals/objectives
Ensure resources are managed effectively in US DMO, including reviewing the productivity and utilization of the group
Provide accurate forecasting figures for the annual budget and manage P&L throughout the year to ensure that the budgetary goals are met or exceeded
Lead and support the continuous improvement and implementation of processes and technologies within DM
Provide technical expertise and solutions to solve problems and improve efficiency across functions, projects and customers
Monitor quality and efficiency across projects to identify trends and opportunities for improvements
Attend customer meetings and leading discussions of project requirements and strategic planning
Exhibit credibility and expertise in Business Development activities with existing and potential new clients
Provide operational input into proposals including participation in client presentations

Candidate Profile

We are looking for a sharp, accomplished person who has the proven management experience to lead a very talented Data Management Operations team, who enjoys interacting with clients, and has previous department and program budgetary responsibilities. It's a great environment and a great opportunity for the right person - maybe for you or maybe someone you know...

Successful candidates will possess a minimum of 10 years experience in clinical development as a clinical data manager in the pharmaceutical industry, at least 5 years demonstrated experience managing a team, and at least 2 years experience with electronic data management systems. A Bachelor's Degree in life sciences, computer programming or other health care related field is required. Candidates with previous Oncology and/or CRO experience are strongly preferred.

In addition, the position also requires superior interpersonal and communication skills; the ability to mentor and coach others in a positive manner; the ability to manage multiple and varied tasks with enthusiasm; the ability to independently exercise professional judgment; the ability to operate effectively in a deadline-driven global environment; a strong client focused approach to work; and a thorough understanding of resource & budget management.

At Cmed we currently offer our Full Time U.S. employees:

Rapid career advancement and training opportunities with a mentoring program
A commitment to work life balance with 20 vacation, 12 holidays, 3 personal days annually, and paid sick time
Increased vacation with years of service
Exciting, state of the art technology
The opportunity to make a difference and be recognized in a dynamic, growing company
Plus many more great benefits

Team Manager Coding

Geographical Location	Horsham, W. Sussex, UK
Contact Information	sthompson@cmedresearch.com
Applications Before	30th September 2008
Remuneration	Competitive

About

If you are an ambitious individual looking for an opportunity to grow professionally and have a direct impact on the success of the company, then we are seeking you to join our growing Coding group based in Horsham, West Sussex. This exciting and highly visible role will enhance your current experience and put you on the path for career advancement. All while gaining exposure to a wide variety of therapeutic areas and studies, experience on a leading-edge electronic clinical trial data acquisition and management system, and satisfaction in your career. We are looking for a sharp, accomplished person who has the proven team management experience to lead a very talented team of Coding managers, who enjoys interacting with clients, and has previous expereince of managing a team or department., to

We provide excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits

Principal Duties and Responsibilities

Manage, direct and co-ordinate all activities and resources for the Coding Team within Data Management Operations. Act as a consultant on the requirements for specific sponsors to ensure that the coding of clinical data is performed as per our sponsors Standard Operating Procedures/Working Practices to ensure Heath Authority Regulations are met. Ensure that coding is of the highest quality so that the clinical database can be locked according to ICH GCP standards.

Provide input into User Acceptance Testing (UAT) specifically for coded term fields and ensure that the correct version of the dictionary has been installed and that the synonym dictionary and the auto-encoding algorithm is functioning correctly. Liaise with the Trial Data Manager and the client to resolve coding problems and queries. Manually encode medical and therapy terms not automatically encoded by the data management system. Generate requests for new Medical and Therapy terms and changes to existing terms with the dictionary provider or client as appropriate. Review consistency and accuracy of medical and therapy terms before producing coding reports for the client. Provide medical terminology and therapy coding reports for the client. Ensure that these reports are approved with signed approval form, prior to database lock. Maintain the synonym dictionary and the algorithm components of the auto-encoder e.g. stop words, stop characters.

Candidate Profile

The successful candidate will hold a life science degree or nursing degree or relevant experience and have a high understanding of medical terminology, clinical trial methodology and ICH/GCP. High level of understanding of physiology, pharmacology, clinical study objectives and the drug development process. They will also have at least 5 years of experience in the coding of clinical data using commercial dictionaries such as WHODRUG, MedDRA preferred, and 3 years experience of supervising or managing a team.

The successful candidate must be comfortable with presenting to customers and acting as a company representative and have a professional, positive and enthusiastic attitude in addition to excellent organisational, planning, resourcing and leadership skills, excellent interpersonal and communication skills and the ability to operate effectively in a global working environment.

A very good investigative and meticulous approach to all activities and tasks. Good negotiation and problem solving skills. Ability to work effectively and efficiently with internal partners.

Principal Clinical Data Manager

Geographical Location	New Providence, NJ, US
Contact Information	lburroughs@cmedresearch.com, +1 214 491 2909
Applications Before	31 Aug 2008
Remuneration	Competitive

About

Tired of the daily grind?
Career and earning prospects going no where fast?
Now imagine yourself working for a company that offers the opportunity to make a difference.
Now imagine yourself working for a company with an emphasis on work life balance.
Now imagine that same company can collect clinical trial data electronically in a remote African village without electricity or access to the internet.

Sound impossible?

At Cmed anything is possible.

We are an eCRO, based in the US and Europe that uniquely combines a Clinical Research Organization and a state of the art technology development company. The operational activities of our CRO division are underpinned by Timaeus. We believe Timaeus is the world's most sophisticated and complete electronic data capture and management system that can work anywhere in the world there is mobile phone or satellite coverage.

Let us show you how we have captured the impossible.

At Cmed we currently offer our Full Time U.S. employees:

Rapid career advancement and training opportunities with a mentoring program
A commitment to work life balance with 20 vacation, 12 holidays, 3 personal days annually, and paid sick time
Increased vacation with years of service
Exciting, state of the art technology
The opportunity to make a difference and be recognized in a dynamic, growing company

As a result of our continued success, we are currently recruiting for experienced Principal Clinical Data Managers for our eDC Center of Excellence in New Jersey.

Principal Duties and Responsibilities

As a Principal Clinical Data Manager you will use your extensive knowledge and data management experience to provide oversight and coordination in the day-to-day management of data management projects ensuring that quality deliverables are on time, within budget and according to client expectations; provide input into proposals regarding resources and study deliverables; serve as primary contact with client to ensure appropriate communication and timely updates; and participate in bid defenses.

In addition to exceptional project management skills, you will also need strong people management and communication skills to effectively lead your internal team. You will have the ability to motivate and provide guidance to the study team. They will look to you as a leader/resource to provide direction/feedback into study related issues. You will review work produced by project teams and ensure all activities are meeting SOPs and client expectations. Plus you will be responsible for creating performance goals and performing staff appraisals for you team, as well as conducting on-to-one and team meetings.

Candidate Profile

Successful candidates will have a Bachelors degree in life sciences or related discipline or equivalent work experience; at least 5 years of Clinical Data Management experience from within the CRO/Pharmaceutical industry with at least 3 years leading and overseeing a CDM team; and be proficient in a Windows environment. Previous experience with eDC (electronic data capture) is strongly preferred.

If your current career path is impossible, what do you have to lose? Just give us a call.

Senior Clinical Data Manager

Geographical Location	New Providence, NJ, US
Contact Information	Lisa Burroughs, lburroughs@cmedresearch.com, + 1 215 491 2909
Applications Before	31 Aug 2008
Remuneration	Competitive

About

Tired of the daily grind?
Career and earning prospects going no where fast?
Now imagine yourself working for a company that offers the opportunity to make a difference.
Now imagine yourself working for a company with an emphasis on work life balance.
Now imagine that same company can collect clinical trial data electronically in a remote African village without electricity or access to the internet.

Sound impossible?

At Cmed anything is possible.

Let us show you how we have captured the impossible.

At Cmed we currently offer our Full Time U.S. employees:

Rapid career advancement and training opportunities with a mentoring program
A commitment to work life balance with 20 vacation, 12 holidays, 3 personal days annually, and paid sick time
Increased vacation with years of service
Exciting, state of the art technology
The opportunity to make a difference and be recognized in a dynamic, growing company

As a result of our continued success, we are currently recruiting for experienced Senior Clinical Data Managers for our eDC Center of Excellence in New Jersey.

Principal Duties and Responsibilities

As a Senior Clinical Data Manager you will use your existing knowledge and experience to provide oversight and coordination of clinical data management activities, on both an individual trial and project level. You will be tasked with management of paper based and eDC trials alike. You will monitor the status and progress of data management activities for assigned projects from study start-up to successful database lock to proactively ensure project deliverables meet sponsor requirements, are on schedule and within budget. Additionally, you will perform and often coordinate the following activities: the development and implementation of the Data Management Plan; implementation, coordination, and documentation of database user acceptance testing; data review; query generation; data coding; electronic data reconciliation; identification of protocol deviations; and project status updates to internal management as well as the Sponsor. Additionally, for eDC trials you will be responsible for coordinating site initiation and evaluation along with on site training of personnel on study specific data capture procedures.

In addition to strong data and project management skills, you will need strong people management and communication skills to work effectively with your internal team, the client, and, in the case of eDC studies, the site. You will have the ability to motivate and provide mentorship to less experienced members of the Data Management team. They will look to you as a leader/resource to provide guidance/input into study related issues.

Candidate Profile

Successful candidates will have a Bachelors degree in life sciences or related discipline or equivalent work experience; at least 4 years of Clinical Data Management experience from within the CRO/Pharmaceutical industry; and be proficient in a Windows environment. Previous experience with eDC (electronic data capture) is strongly preferred.

Position also requires superior interpersonal and communication skills; attention to detail; the ability to independently exercise professional judgment; the ability to operate effectively in a deadline driven global environment; and an understanding of resource & budgeting.

If your current career path is impossible, what do you have to lose? Just give us a call.

Principal Clinical Data Manager

Geographical Location	Horsham, W. Sussex, UK
Contact Information	sthompson@cmedresearch.com, +44 1403 755050
Applications Before	30th September 2008
Remuneration	Competitive

About

Are you an extremely motivated, highly experienced Senior Clinical Data Manager who is looking for an opportunity to grow professionally and have a direct impact on the success of the company? If so, consider joining our team in our Horsham Office, West Sussex. This exciting and highly visible role will enhance your current experience and put you on the path for career advancement. All while gaining exposure to a wide variety of therapeutic areas and studies, experience on a leading-edge electronic clinical trial data acquisition and management system, and satisfaction in your career. We are looking for a sharp, talented person who works well independently, has the expertise to champion projects, who enjoys interacting with clients and motivating a team, but who can also have some fun and work well in a growing global team. It's a great environment and a great opportunity for the right person - maybe for you...

Principal Duties and Responsibilities

Candidate Profile

We offer a competitive benefits package, a pleasant working environment that stresses individual and team achievements, a commitment to work life balance, and outstanding career opportunities.

Senior Clinical Data Manager

Geographical Location	Horsham, W. Sussex, UK
Contact Information	sthompson@cmedresearch.com, +44 1403 755050
Applications Before	30th September 2008
Remuneration	Competitive

About

Are you a highly motivated, experienced Clinical Data Manager who is looking for an opportunity to have a direct impact on the success of the company and have your achievements recognized by Senior Management? If so, consider becoming a Senior Clinical Data Manager at Cmed (CRS) Ltd in our Horsham. West Sussex Office. This exciting and vital role will enhance your current experience and put you on the path to career advancement. In addition, you will gain exposure to a wide variety of therapeutic areas and studies, experience on a leading-edge electronic clinical trial data acquisition and management system, and satisfaction in your career.

Principal Duties and Responsibilities

Candidate Profile

Clinical Data Manager

Geographical Location	New Providence, NJ, US
Contact Information	Lisa Burroughs, lburroughs@cmedresearch.com, + 1 215 491 2909
Applications Before	31 Aug 2008
Remuneration	Competitive

About

Tired of the daily grind?
Career and earning prospects going no where fast?
Now imagine yourself working for a company that offers the opportunity to make a difference.
Now imagine yourself working for a company with an emphasis on work life balance.
Now imagine that same company can collect clinical trial data electronically in a remote African village without electricity or access to the internet.

Sound impossible?

At Cmed anything is possible.

Let us show you how we have captured the impossible.

At Cmed we currently offer our Full Time U.S. employees:

Rapid career advancement and training opportunities with a mentoring program
A commitment to work life balance with 20 vacation, 12 holidays, 3 personal days annually, and paid sick time
Increased vacation with years of service
Exciting, state of the art technology
The opportunity to make a difference and be recognized in a dynamic, growing company

As a result of our continued success, we are currently recruiting for experienced Clinical Data Managers for our eDC Center of Excellence in New Jersey.

Principal Duties and Responsibilities

As a Data Manager you will provide input into the professional management and coordination of clinical trial data (Phases I to IV). Ensure ongoing data entry from CRFs or other sources into the clinical trial database within agreed time frames to a high standard of accuracy. Identify, resolve or query problematical data observed during data entry raised by electronic checks or manual review. Perform timely update of tracking databases in order to maintain an accurate status of data processing (e.g. data entered, cleaned and QC'd). Potential to act as Trial Data Manager. Communicate effectively as appropriate with the client e.g. via e-mail with monitors in order to manage allocated data. Contribute into the design and usability testing of new databases and validation programming.

Candidate Profile

Ideally successful candidates will have a Bachelors degree in life sciences or related discipline or equivalent work experience; at least 2 years of Clinical Data Management experience from within the CRO/Pharmaceutical industry; and be proficient in a Windows environment. Previous experience with eDC (electronic data capture) is strongly preferred.

Position also requires excellent communication skills; attention to detail; the ability to independently exercise professional judgment; and the ability to operate effectively in a deadline driven global environment.

If your current career path is impossible, what do you have to lose? Just give us a call.

Clinical Data Associate II

Geographical Location	Horsham, W. Sussex, UK
Contact Information	Sarah Thompson, sthompson@cmedresearch.com, 01403 755050
Applications Before	30th September 2008
Remuneration	Competitive

About

We are seeking ambitious individuals to join our growing clinical data management group based in Horsham, West Sussex, to support paper based and electronic data capture clinical trials. We provide excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits

Principal Duties and Responsibilities

Provide input into the professional management and coordination of clinical trial data (Phases I to IV). Ensure ongoing data entry from CRFs or other sources into the clinical trial database within agreed time frames to a high standard of accuracy. Identify, resolve or query problematical data observed during data entry raised by electronic checks or manual review. Perform timely update of tracking databases in order to maintain an accurate status of data processing e.g. data entered, cleaned and QC'd. Be able to provide status information on allocated data to the Trial Data Manager. Communicate effectively as appropriate with the client e.g. via e-mail with monitors in order to manage allocated data. Contribute into the design and usability testing of new databases and validation programming.

Candidate Profile

We are seeking Life Science graduates (or equivalenet qualifications) for entrance Data Management positions (CDA II), to join our rapidly growing Clinical Data Management group based in Horsham, West Sussex. Successful candidates will become part of a fast paced and highly innovative team as a Clinical Data Associate II and as such will be responsible for supporting clinical trial data management at the cutting edge. Ideally degree in life sciences, pharmacy, nursing or nursing qualification (e.g. RN) but equivalent degree level qualifications considered. Good organisational, interpersonal and communication skills and the ability to operate effectively in a team environment. The individual needs to be able to work calmly under pressure and meet deadlines. A dynamic individual with a professional, positive and enthusiastic attitude. The individual should have a basic understanding of medical terminology, clinical trial methodology and ICH/GCP and the drug development process. They should have an investigative and meticulous approach to all activities and tasks and proven ability with clinical databases or equivalent.

Clinical Data Manager

Geographical Location	Horsham, W. Sussex, UK
Contact Information	Sarah Thompson, sthompson@cmedresearch.com, 01403 755050
Applications Before	30th September 2008
Remuneration	Competitive

About

We are seeking ambitious individuals to join our growing clinical data management group based in Horsham, West Sussex, to support "paper based" and "electronic data capture" clinical trials. We provide excellent training, personal development, career opportunities, international placements and a competitive package of salary, pension, private healthcare and other benefits

Principal Duties and Responsibilities

Provide input into the professional management and coordination of clinical trial data (Phases I to IV). Ensure ongoing data entry from CRFs or other sources into the clinical trial database within agreed time frames to a high standard of accuracy. Identify, resolve or query problematical data observed during data entry raised by electronic checks or manual review. Perform timely update of tracking databases in order to maintain an accurate status of data processing (e.g. data entered, cleaned and QC'd). Potential to act as Trial Data Manager. Communicate effectively as appropriate with the client e.g. via e-mail with monitors in order to manage allocated data. Contribute into the design and usability testing of new databases and validation programming.

Candidate Profile

Ideally degree in life sciences, pharmacy, nursing or nursing qualification (e.g. RN) but equivalent degree level qualifications considered. Typically at least 2 years experience in clinical trials ideally in the discipline of data management. Good organisational, interpersonal and communication skills and the ability to operate effectively in a team environment. The individual needs to be able to work calmly under pressure and meet deadlines. A dynamic individual with a professional, positive and enthusiastic attitude. The individual should have a basic understanding of medical terminology, clinical trial methodology and ICH/GCP and the drug development process. They should have an investigative and meticulous approach to all activities and tasks and proven ability with clinical databases or equivalent.