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Customer Service Representative with French or Italian

2010-09-08 00:00:00

Title: Customer Service Representative with French or Italian
Salary: Not Disclosed
Location: Limerick - Ireland
Languages: English, French, Italian
Posted: 8th Sep 2010

Description:
Cook Medical�, is a dynamic and innovative US multinational medical device company, a world-leader in the field of minimally invasive medical devices, offers exciting opportunities to join their team. We are currently recruiting for an Customer Service Representative with fluent Italian to join our team.

The main focus of this role is to provide a professional, friendly and efficient service to customers throughout Europe. Input customer orders to the Cook European order-entry system and provide timely and accurate responses to customer queries.

The ideal candidate will have:

- Leaving Certificate or equivalent and relevant certificate/diploma.
- Fluency in Italian or French and English
- Excellent telephone manner and interpersonal skills.
- Excellent data entry skills
- Computer literacy: Good working knowledge of Microsoft� Office.
- Positive attitude and proven problem-solving skills.
- Availability and willingness to travel on company business. Representatives may be required to spend time overseas for training purposes.

Please note you may be asked to complete an on line interview for this position.

Bilingual Client Relationship Manager

2010-09-07 00:00:00

Title: Bilingual Client Relationship Manager
Salary: �20,000
Location: Dublin - Ireland
Languages: English, French, Flemish
Posted: 7th Sep 2010

Description:
Client Relationship Manager

Our client, a global multinational pharmaceutical and medical device company with a prestigious product portfolio requires a motivated self starter to join their Sales Development Team. Focusing on the EMEA region the Sales Development Representative will have a proactive, technical and professional approach to this elite sales market.

This is a new initiative to target and develop a new market segment. The person will have a very prestigious product to offer prospective clients who are in a growing market segment.

Duties:

� Manage and maintain a database of accounts with associated Sales Revenue and Key Performance targets
� Strengthen existing relationship with customers and initiate new customers
� Discover how customers use their promotional products and prepare consultative promotional solutions to meet each customer�s unique situation
� Coordinate with other departments as necessary to meet customer expectations
� Participation in product projects when required

Ideal Candidate:

� Good telephone manner: courteous, clear speech, good call management, assertive and professional
� Educated to degree level in Human Biological Sciences, Pharmacy or other relevant course.
� Be fluent in one of the following languages: English, French, Flemish.
� Have previous experience within a sales environment, particularly direct sales and with a proven sales ability preferably in the pharmaceutical or medical device.
� Be adept at identifying and developing new sales opportunities for the company
� Have the ability to maintain professionalism under pressure
� Be computer literate, with good keyboard skills; familiar with different on-line data-base packages
� Possess good communication and listening skills with a pleasant telephone manner
� Possess good problem solving skills
� Be a good team player

Bilingual Client Relationship Manager

2010-09-07 00:00:00

Title: Bilingual Client Relationship Manager
Salary: �20,000
Location: Dublin - Ireland
Languages: German, Italian, Spanish
Posted: 7th Sep 2010

Description:
Client Relationship Manager- Germany

Our client, a global multinational pharmaceutical and medical device company with a prestigious product portfolio requires a motivated self starter to join their Sales Development Team. Focusing on the German region the Client Relationship Manager will have a proactive, technical and professional approach to this elite sales market.

The person will have a very prestigious product to offer prospective clients who are in a growing market segment.

Duties:

� Manage and maintain a database of accounts with associated Sales Revenue and Key Performance targets
� Strengthen existing relationships with customers and initiate new customers
� Discover how customers use their promotional products and prepare consultative promotional solutions to meet each customer�s unique situation
� Coordinate with other departments as necessary to meet customer expectations
� Participation in product projects when required

Ideal Candidate:

� Good telephone manner: courteous, clear speech, good call management, assertive and professional
� Educated to degree level in Human Biological Sciences, Pharmacy or other relevant course.
� Be fluent in one of the following languages: Italian, Spanish, German.
� Have previous experience within a sales environment, particularly direct sales and with a proven sales ability preferably in the pharmaceutical or medical device.
� Be adept at identifying and developing new sales opportunities for the company
� Have the ability to maintain professionalism under pressure
� Be computer literate, with good keyboard skills; familiar with different on-line data-base packages
� Possess good communication and listening skills with a pleasant telephone manner
� Possess good problem solving skills
� Be a good team player

Operations Supervisor with European Language

2010-09-07 00:00:00

Title: Operations Supervisor with European Language
Salary: Negotiable
Location: Dublin - Ireland
Languages: English, Swedish, Bulgarian
Posted: 7th Sep 2010

Description:
Berkley Pharmaceutical and Life Sciences is currently recruiting an Operations Supervisor to be based in Ireland, Bulgaria or Sweden

This is an expanding company and the role will sit in a new European hub for Medical Communications working with a top Pharmaceutical organisation.

Role/Opportunity
� The Operations Supervisor is responsible for the day to day operations of the medical information/call center project team.
� Providing support to staff members so that contracted services are provided in accordance with client and company policies and procedures and within regulatory guidelines.
� Responsible for the training and supervision of medical information staff, including Medical Information Associates and/or Customer Assistance Specialists.
� An integral part of this supervision is the development, coaching, and mentoring of the consultants to ensure quality operations.
� Maintain client relationships

Skills/Experience
� BS in Pharmacy
� 4-5 years experience
� Some projects may allow for the following requirements; BSN or equivalent experience, RN license OR significant experience in the healthcare or pharmaceutical industry with responsibilities involving counselling or providing medical information.
Or equivalent combination of education, training and experience that provides the knowledge, skills and abilities to perform the job.
� Supervisory experience preferred
� Pharmacovigilance experience preferred
� Multi-lingual - proficient in English and at least one other required language

Berkley Pharmaceutical and Life Sciences is a specialist recruitment consultancy which recruits pharmaceutical, clinical and medical device professionals throughout Ireland, Asia, UK and Australia

Dutch speaking Technical Sales

2010-09-07 00:00:00

Title: Dutch speaking Technical Sales
Salary: �24,000 - �26,000
Location: Glasgow Area - Scotland, United Kingdom
Languages: English, Dutch
Posted: 7th Sep 2010

Description:
Our client, a well established Company based outside Glasgow require a fluent Dutch speaker reporting to the Divisional Sales Manager. The successful candidate will be fluent in both Dutch and English with first class communication and interpersonal skills. The role will be to develop business within the food and drink industry and commercial laboratories selling the company product. The role involves extensive customer service, selling and maximising on customer accounts, providing customer support, face to face demonstrations and troubleshooting.

The successful candidate will be a highly ambitious, enthusiastic self-starting candidate with excellent organisational and multi-tasking skills. A life science background and or experience within the food industry would be highly advantageous. A desire to meet and exceed sales targets is a must and candidates will benefit from a competitive commission structure.

This is an excellent opportunity for recent Graduates with a Degree in Sciences, or those candidates looking to progress their career with a rapidly expanding organisation.

If you require any information, please call Lisa Slipchuk on 0141 243 4490 or email your CV to lisa.slipchuk@pertemps.co.uk

German speaking Technical Sales Executive

2010-09-07 00:00:00

Title: German speaking Technical Sales Executive
Salary: �24,000
Location: Glasgow Area - Scotland, United Kingdom
Languages: English, German
Posted: 7th Sep 2010

Description:
Our client, a well established Company based outside Glasgow require a fluent German speaker reporting to the Divisional Sales Manager. The successful candidate will be fluent in both German and English with first class communication and interpersonal skills. The role will be to develop business within the food and drink industry and commercial laboratories selling the company product. The role involves extensive customer service, selling and maximising on customer accounts, providing customer support, face to face demonstrations and troubleshooting.

The successful candidate will be a highly ambitious, enthusiastic self-starting candidate with excellent organisational and multi-tasking skills. A life science background and or experience within the food industry would be highly advantageous. A desire to meet and exceed sales targets is a must and candidates will benefit from a competitive commission structure.

This is an excellent opportunity for recent Graduates with a Degree in Sciences, or those candidates looking to progress their career with a rapidly expanding organisation.

If you require any information, please call Lisa Slipchuk on 0141 243 4490 or email your CV to lisa.slipchuk@pertemps.co.uk

Scientific Inside Sales

2010-09-07 00:00:00

Title: Scientific Inside Sales
Salary: OTE �25k +
Location: Glasgow Area - Scotland, United Kingdom
Languages: French, German, Swedish
Posted: 7th Sep 2010

Description:
An opportunity is available with a leading international supplier of research instrumentation and consumables across the biotechnology and life sciences markets. Our client is looking for a Inside Sales Representative working with their range of customers across the European markets. Applicants should ideally have a degree in biology and be fluent in one of the following languages, French, Spanish, Danish, Swedish.
The role is an entry level position, is based in Scotland and offers an on target package of �25k +.
Qualifications and Experience:
� BSc (or higher) in biological/chemical sciences
� General laboratory experience and familiarity in laboratory instrumentation both hardware and software
� Strong computer skills
� Fluency in English, fluency in a second European language (French, German, Swedish, Danish, Spanish)
� Customer facing or telephone sales experience would be advantageous
The ideal candidate will be an excellent communicator with strong customer focus. Also you will also be well organised, and able work independently.
To apply for this position please send your CV to scientific@inveniaresourcing.com or call +44 (0)113 3662014.

CLINICAL RESEARCH ASSOCIATE - LISBON

2010-09-03 00:00:00

Title: CLINICAL RESEARCH ASSOCIATE - LISBON
Salary:
Location: Lisboa - Portugal Centro, Portugal
Languages: English, Portuguese
Posted: 3rd Sep 2010

Description:
Responsibilities include: Perform site selection, initiation, monitoring and close-out visits. Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. May provide assistance to less experienced clinical staff.

Successful candidates will hold a Degree, in a scientific or healthcare discipline, advanced level of English, complimented all by solid prior monitoring experience.

A competitive salary is on offer and this is an urgent requirement so for immediate consideration and a full job description on a request please forward your CV to beatriz.deluis@secpharma.com or call + 44 (0) 207 255 6600

Swedish/Dutch - Scientific Sales Associate - Based in Glasgow, Scotland

2010-09-03 00:00:00

Title: Swedish/Dutch - Scientific Sales Associate - Based in Glasgow, Scotland
Salary: �Market Rate + Benefits
Location: Glasgow Area - Scotland, United Kingdom
Languages: Dutch, Swedish
Posted: 3rd Sep 2010

Description:
This highly reputable and progressive organisation seeks ambitious and enthusiastic Swedish/Dutch speaking Life Science/Biotechnology graduates to add value to their fast paced, commercial sales team based near Glasgow. Your key remit will include researching and developing relationships with target companies within the Life Sciences sector.

This role is primarily telephone and email based and requires excellent communication skills along with the ability to build lasting business relationships with both clients and colleagues. Candidates will ideally be of graduate calibre and have some experience in a targeted sales environment.

An excellent opportunity to kick-start your career in the life sciences industry with a first class, global organisation.

Clinical Study Manager

2010-09-03 00:00:00

Title: Clinical Study Manager
Salary: €70000 - €85000 per annum + Bonus + Benefits inc relocation
Location: Switzerland
Languages: English
Posted: 3rd Sep 2010

Description:
A leading Pharmaceutical company with an excellent reputation for retaining some of the brightest talent in the industry, currently has five vacancies for Clinical Managers to join their hugely sucessful team!!

This opportunity will enable you to increase your experience and allow you to develop your career within a global context.

You will serve as a Clinical Manager supporting the study data cleaning while actively ensuring quality, consistency and integration of study data. You will lead and participate in the preparation and delivery of study documents while facilitating strong external partnerships and work with marketing companies, CRO's and academic clinics to identify and resolve operational feasibility issues.

To apply for this role you must have a University degree in biological science, health related field or licensed registered nurse, strong communication skills and demonstrate relevant industry or health related experience. A good candidate will be able to recognize safety data trends and have a thorough understanding of clinical trial design on Oncology. Field monitoring experience is an advantage. This role would ideally suit an experienced Senior CRA or Clinical Project Manager.

In return you will receive the finest training and advancement opportunities offering a supportive development environment.

For immediate consideration please forward your CV to james.brown@secpharma.com or call + 44 (0) 207 255 6600 for further details

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business

CLINICAL RESEARCH ASSOCIATE II - 'ONCOLOGY' STUDY, PHASE II-III

2010-09-03 00:00:00

Title: CLINICAL RESEARCH ASSOCIATE II - 'ONCOLOGY' STUDY, PHASE II-III
Salary: NEGOTIABLE
Location: Croatia
Languages: English, Croatian
Posted: 3rd Sep 2010

Description:
My client is a leading international CRO in Croatia and currently is looking for a Clinical Research Associate II (CRA II) with strong experience in monitoring the clinical trials, ready for a challenging job in an international organization. The successful applicant will have the opportunity to work on varied projects, therapeutic areas and phases of development. This is a full-time, office based position.

Challenges:

The responsibility of a Clinical Research Associate II (CRA II) is to perform the full clinical monitoring aspect of the assigned projects in accordance with Company's SOPs and GCP. The duties will span from feasibility visits, pre-study and study initiation visits, through the preparation of the concise reports of monitoring visits to performing the close-out activities in compliance with regulatory requirements. Overall you will ensure the completeness and accuracy of all study aspects, submit RA and EC submission documentation, coordinate all study material and site related study documentation. Additionally, you will assess, monitor and train study site staff as required.

Experience

Ideally you will have a degree in Medicine or Pharmacy and cardiovascular experience but other life science degree (biology, physical or health studies, nursing degree) is acceptable with at least 2 years monitoring experience. You will have a thorough understanding of clinical research principles and processes, and will be able to work diligently and methodically. You will have strong interpersonal skills and be a team player. Additionally, you will posses excellent planning and organizational skills with effective time management and exceptional oral and written communication skills both in Croatian and English language.

If you are interested in this opportunity or know somebody who might be suitable/interested, please feel free to contact me or pass my contact details for further information.
To apply please send your CV to Matus.Hlivjak@secpharma .com or contact me on 0044 207 255 6600 for additional information.

Senior SAS Programmer - Switzerland

2010-09-03 00:00:00

Title: Senior SAS Programmer - Switzerland
Salary: €85000 - €100000 per annum
Location: Switzerland
Languages: English, French, German
Posted: 3rd Sep 2010

Description:
Senior SAS programmer – Switzerland

A leading pharmaceutical company are currently seeking an expert SAS programmer to oversee implementation of projects and potentially move on to manage a team. This is an ideal position for an experienced programmer with aspirations to reach the highest level.

Responsibilities:

Implementation, development and maintenance of systems that analyze and report on clinical data using SAS and other data analysis and database tools.
Engage in constant stake-holder management throughout projects to ensure a positive experience for end-users.
Trouble-shooting and presenting technical solutions to the project team.
Maintaining up to date documentation for system and quality standard requirements.
Recommend and develop new processes, standards and procedures for system use.

Qualifications and skills:

Excellent SAS programming knowledge
Understanding of data management procedures
Working with large, complex datasets to create table and listings and generate reports.
Excellent communication and stakeholder management skills
Previous managerial or supervisory experience would be advantageous

For immediate consideration please forward your CV to simon.boorman@secpharma.com or call 0207 255 6600 and ask for Simon Boorman.

Key words: SAS, statistical programmer, BASE, MACRO, GRAPH, STAT, clinical trials, pharmaceutical, CRO Switzerland, Zurich, Geneva, Basel

Head of Clinical Research & Development

2010-09-03 00:00:00

Title: Head of Clinical Research & Development
Salary: €120000 - €130000 per annum + Bonus + Benefits
Location: Germany
Languages: English
Posted: 3rd Sep 2010

Description:
My client a leading Pharmaceutical company who has recently reported some impressive quarterly results and has undergone a sustained period of growth owing to an innovative and revered pipeline, currently has a high profile opening for a Head of Clinical Research Development to join their R&D team.

Within this role you will assume responsibility for the region (Northern & Central Europe) and be responsible for planning and execution of all clinical studies in the region while assuming management of the Global Clinical Research team working within this region (initially 26 employee’s rising to 80 as responsibility grows).

This is a multifunctional role incorporating Operational Management, Scientific and Strategic input and finally direct line management and will require an individual who is able to handle working within this type of environment.

Suitable applicants will hold an advanced University Degree (MD is desirable though not essential) and have extensive experience in clinical studies for pharmaceutical products across all phases of development. You must have experience managing/building a successful multi-national team and an in depth knowledge of clinical trial methodology and operations. English is the only language required for this position however additional European languages are an advantage.

In return my client can offer a unique opportunity to join a fast-growing company in a business critical position. A competitive salary and benefits package would be available to suitable applicants including relocation assistant where appropriate.

For immediate consideration and a full job description please forward your CV to james.brown@secpharma.com or call + 44 (0) 207 255 6600

CLINICAL RESEARCH ASSOCIATE

2010-09-03 00:00:00

Title: CLINICAL RESEARCH ASSOCIATE
Salary:
Location: Barcelona - Spain
Languages: English
Posted: 3rd Sep 2010

Description:

Responsibilities include: Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. May provide assistance to less experienced clinical staff.

Successful candidates will hold a Degree, in a scientific or healthcare discipline and, will have an excellent command of English in all complimented by solid prior monitoring experience and lead CRA responsibilities: Your expertise as a Senior or Lead CRA will ensure that clinical stages of research projects are completed in accordance with customer high expectations

In return my client offers career opportunities providing flexibility and growth across the organisation, competitive salary and benefits package, work-life balance initiatives and social events. This is an urgent requirement so for immediate consideration and a full job description on a request please forward your CV to beatriz.deluis@secpharma.com or call + 44 (0) 207 255 6600

Director of Market Access & Health Economics

2010-09-03 00:00:00

Title: Director of Market Access & Health Economics
Salary:
Location: South East, United Kingdom
Languages: English
Posted: 3rd Sep 2010

Description:
Due to their continued growth, my client is looking for a Director of Health Economics and Market Access to join their London based office. This is a fantastic opportunity to join a highly respected global company and shape both Market Access strategy and the direction and development of a new department. The company, a London based consulting firm has offices in both Europe and the USA, and can call a number of the world’s largest pharmaceutical companies its clients.

To find out more about this position call Will Guy on 0044 207 255 6665 for a confidential discussion or email william.guy@secpharma.com.

In this post you will responsible for:

•Setting up the new Health Economics and Market Access department.
•Assisting in business development by helping to maximise relationships with clients and contacts.
•Providing HE/MA support for project teams, including group training and individual mentoring.
•Undertaking direct or shared supervision of projects with challenging HE/MA content.
•Providing input into the strategic development of the company.

To be considered for this role you should possess the following skills and experience.
•MSc in Health Economics or a closely related discipline
•At least 3 years’ experience in a health economics/market access role within the healthcare industry, preferably in a global environment.
•Excellent written and spoken English

Due to logistical and legal reasons my client can only consider candidates who already have to correct documentation to work within the UK.

To apply forward your CV to william.guy@secpharma.com with a short cover note detailing your salary expectations and suitability for the position. Alternatively call Will Guy 0044 207 255 6665 for further information and a confidential discussion on this and other opportunities within the industry.
SEC are an ISO9001:2000 accredited specialist Recruitment Company working within the Pharmaceutical, Biotech and CRO industries. If you are interested to learn more about further appointments within HEOR or Market Access across the UK and Mainland Europe contact Will Guy on 020 7 255 6665 for a confidential discussion.

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business

Senior Director CNS

2010-09-03 00:00:00

Title: Senior Director CNS
Salary: �110000 - �130000 per annum + Benefits
Location: Derbyshire - East Midlands, United Kingdom
Languages: English
Posted: 3rd Sep 2010

Description:
My client an expanding Contract Research Organisation currently has an exciting high profile opportunity to join their organization. Owing to growth my client has recently restructured into four therapeutic pillars offering further client development opportunities around their four core therapeutic specialties. As a result of this restructure they are currently seeking a Senior Director to head up the CNS Global Division.

Based anywhere in my clients network of office’s in the EMEA or from home you will assume overall responsibility for the CNS group. Your principal responsibilities will include but not be limited to; line management of the CNS group incorporating recruitment, training, development and performance review of personnel. Coupled with this you will take on Program management responsibilities for all CNS studies currently being undertaken by my client. You will oversee, and conduct budget reviews and provide financial analysis support as and where required.

The suitable applicant will be tasked with working with existing sponsors to further promote growth within the CNS group, and in cooperation with business development and senior management assist in strategic acquisition of new business.

Suitable applicants will be degree educated or hold a nursing equivalent qualification and have long proven track record working within CNS. This will include managing Global Studies and ideally incorporate line management of personal up to Project Director level. You will have superior leadership and interpersonal skills and a proven ability to negotiate with clients in a professional manner.

You must hold a fluency in English and additional European languages are highly desirable.
In return my client can offer a competitive salary and remuneration package and the opportunity to work in a business critical role within a rapidly growing organization realizing your passion in CNS. Flexibility will be offered to office (where appropriate) or home-based working and travel is approximated at 30 %.

Urgent consideration will be given to suitable applicants, to apply or for further information please forward your CV to james.brown@secpharma.com or call + 44 (0) 207 255 6600.

Clinical Project Manager

2010-09-03 00:00:00

Title: Clinical Project Manager
Salary: €600 - €700 per day
Location: Switzerland
Languages: English
Posted: 3rd Sep 2010

Description:
My client is a pioneer in discovering and developing innovative products. Employees become part of an exciting and dynamic global team – they are committed to finding the best, and are now looking for a Clinical Study Manager to join their team in Basel on a 6 month contract.

You will be working in their oncology department and your responsibilities will include the design and management of the trial(s). You will be expected to work independently and collaboratively on a project; coordinating Clinical Research Organisation’s and also assisting and supporting the team.

A suitable candidate will have a BS / BA in Biological Sciences or a nursing equivalent with 3 years experience in the clinical trials environment. Experience in clinical trial design, trial monitoring practices and the drug development process is essential. A demonstrable amount of experience in the Oncology/Hematology area would also be a bonus. Successful candidates should also have a notice period of 1 month or less.

My client is offering a very competitive rate and the opportunity for a strong candidate to have a high extension possibility.

For immediate consideration and a full job description please send through your full CV to Lauren at Lauren.McCarthy@secpharma.com or call +44 207 255 6600.

SENIOR CLINICAL RESEARCH ASSOCIATE-VALENCIA

2010-09-03 00:00:00

Title: SENIOR CLINICAL RESEARCH ASSOCIATE-VALENCIA
Salary:
Location: Spain
Languages: English, Spanish
Posted: 3rd Sep 2010

Description:
Responsibilities include: Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports and other required study documentation. May provide assistance to less experienced clinical staff.

Successful candidates will hold a Degree, in a scientific or healthcare discipline and, will have an excellent command of English in all complimented by solid prior monitoring experience and lead CRA responsibilities: Your expertise as a Senior or Lead CRA will ensure that clinical stages of research projects are completed in accordance with customer high expectations

In return my client offers career opportunities providing flexibility and growth across the organisation, competitive salary and benefits package, work-life balance initiatives and social events. This is an urgent requirement so for immediate consideration and a full job description on a request please forward your CV to beatriz.deluis@secpharma.com or call + 44 (0) 207 255 6600

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business

VB.NET Developer - Global End Client

2010-09-03 00:00:00

Title: VB.NET Developer - Global End Client
Salary: €60000 - €85000 per annum + BENEFITS
Location: Switzerland
Languages: German
Posted: 3rd Sep 2010

Description:
VB.NET Developer - Perm- Basel, Switzerland- up to 90K - 120KCHF

Note : Candidates must be EU nationals and Fluent in German and English

My client is a global end client based in Switzerland and are recruiting for VB.NET Developer with fluency in German and English. They have the ability to attract and retain the brightest talent in the industry and have ambitious plans to keep improving and growing and are looking for people as innovative as themselves.

Job Responsibilities
- Developing Financial Data Warehouse using VB.NET WinForms (Visual Studio 2008)
- Fulfilling given development tasks independently including testing and presenting the solution to customers
- Taking over responsibility for projects
- Creating development standards and keeping documentation up to date

Candidate Requirements
- Information Technology education
- At least 2 - 3 years VB.NET experience
- Strong relational data base know how (SQL Server, DB2, Oracle)
- Expert in SQL (DDL, DML)
- Financial Reporting experience
- Good team player and used to work in a lively, international environment
- Open for new and changing environments
- Customer focused and solution oriented
- Fluency in English and German

In return, you will be offered an excellent competitive salary and generous social benefits. You will have the possibility for development and advancement within a constantly growing company. You will have the chance to work in an innovative, stimulating and multicultural environment.

How to apply

For immediate consideration or for more information, please forward your CV to Liz CRANE at SEC Recruitment.

You must be eligible to work in Switzerland (Swiss National, EU National or Swiss Permit).

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business

CRA I/II, SrCRA

2010-09-03 00:00:00

Title: CRA I/II, SrCRA
Salary: $2200 - $3600 per month + Negotiable
Location: Russia
Languages: English, Russian
Posted: 3rd Sep 2010

Description:
Our client is one of the leading global CRO and currently is looking to hire experienced Clinical Research Associates in various grades (CRA I/II, SrCRA) to monitor their clinical research studies.

You will be responsible for the monitoring cycle of the clinical study from site selection, initiation through the monitoring visits, provide support in RA and EC submissions, study tracking and close-out visits.

The successful candidate will have medical/science background with wealth of independent clinical monitoring experience. The position is office based and candidate must be fluent in Russian and English language both spoken and written. The successful applicant will possess good oral and written communication skills will be computer literate and will have the ability to review and evaluate clinical data.

For the successful candidates company offers a competitive salary, ongoing development, learning plans and training.

If you are interested in this position or know someone who might be suitable/interested, please feel free to contact me or pass my contact details for further information.

To apply, please send your CV to Matus.Hlivjak@secpharma.com or alternatively call on 0044 207 255 6600 for additional details.

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business.