| Job Field | Grade | Speciality | Region | Actions |
| Clinical Research | Any Grade | CRA | Any Location (United Kingdom) | Details |
| I am currently seeking Clinical Research Associates (CRA's) of all levels, preferably of one years experience and above.
The positions are on a permanent contract and are either office or home based in various locations across the country.
The client is a large international Contract Research Organisation (CRO) who have a global presence.
Call Paul on 0044 1293 776 644 or email on... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Any Grade | CRA | Any Location (Spain) | Details |
| I am currently seeking Clinical Research Associates (CRA's) of all levels, preferably of one years experience and above.
The positions are on a permanent contract and are either office or home based in various locations across the country.
The client is a large international Contract Research Organisation (CRO) who have a global presence.
Call Nick on 0044 1293 776 644 or email on... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Any Grade | CRA | Any Location (Spain) | Details |
| An excellent opportunity for Clinical Research Associates with one years experience looking to take the next step in their clinical careers. This position provides a great chance for those willing to take a step over to a dynamic and expanding CRO. Excellent career potential and training provided within a dynamic and expanding company.
REQUIREMENTS:
My client is looking for personnel to... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Any Grade | CRA | Any Location (United Kingdom) | Details |
| My client requires an experienced CRA for a new position arising due to new studies in the United Kingdom.
The successful candidate can be either field or office based in the South or the Midlands. If you are field based you will need to be able to go to the offices in either the South or the Midlands as required.
You will have at least 3 years CRA experience with a minimum of 12 months... [Full Details] |
| Salary: Negotiable (30000 - 40000 £) |
| Clinical Research | Any Grade | Any Discipline | Any Location (China, Hong Kong,... | Details |
| A Leading Global CRO is looking for a QA Auditor in the Asia Pacific region.
* Heavy Travel is to be expected with this position (Hong Kong and other countries).
* Ability to speak Mandarin is a must. Clinical GCP Auditing (Internal & External) in Asian region experience required.
* Looking at 1+ year's worth of experience.
If interested, contact Tommy at +65 6597 7008 and email... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Regulatory Affairs | London (United Kingdom) | Details |
| Senior Regulatory Affairs Consultant (Biopharm) – London
Introduction
Our client is seeking to appoint a new Senior Regulatory Affairs Consultant (Biopharm). The Senior Regulatory Affairs Consultant (Biopharm) will be experienced in Bio-Pharmaceutical markets gained within CRO/Consultancy or Pharmaceutical companies.
Client Profile
The client is one of the longest established and... [Full Details] |
| Salary: Negotiable (35000 - 45000 £) |
| Regulatory And Drug Safety | Any Grade | QA | Buckinghamshire (United Kingdom) | Details |
| Senior Quality Compliance Associate / Senior GLP Auditor - Buckinghamshire or Home based or Any EU Location
Introduction
Our client is seeking to appoint a Senior Quality Compliance Associate / Senior GLP Auditor. The Senior Quality Compliance Associate / Senior GLP Auditor will conduct GLP audits of investigator sites, vendors, databases and study reports.
Client Profile
The... [Full Details] |
| Salary: Negotiable (34000 - 35000 £) |
| Regulatory And Drug Safety | Any Grade | QA | Hampshire (United Kingdom) | Details |
| Senior Quality Assurance Associate – Hampshire
Introduction
Our client is seeking to appoint a new Senior Quality Assurance Associate. The Senior Quality Assurance Associate will be responsible for working with vendors supporting regulatory inspections, GMP support / compliance and ensuring technical agreements are in place with vendors and reviewing them on a regular basis. GMP auditing... [Full Details] |
| Salary: Negotiable (41000 - 48000 £) |
| Regulatory And Drug Safety | Any Grade | Regulatory Affairs | London (United Kingdom) | Details |
| Regulatory Affairs Officer (Department Lead) - London
Introduction
Our client is seeking to appoint a new Regulatory Affairs Officer. The Regulatory Affairs Officer will provide both technical and administrative expertise to new and existing licenses. The Regulatory Affairs Officer will be the main person responsible within the business for Regulatory Affairs and therefore this person must... [Full Details] |
| Salary: Negotiable (23000 - 26000 £) |
| Regulatory And Drug Safety | Any Grade | Regulatory Affairs | Nottinghamshire (United Kingdom) | Details |
| Regulatory Affairs Manager – Nottingham
Introduction
Our client is seeking to appoint a new Regulatory Affairs Manager. The Regulatory Affairs Manager will have CTA experience along with line managment experience as this person will be managing a team of 3-5 people. The Regulatory Affairs Manager should have investigational medicinal product (IMP) experience with hands on clinical trials... [Full Details] |
| Salary: Negotiable (55000 - 65000 £) |
| Regulatory And Drug Safety | Any Grade | Regulatory Affairs | London (United Kingdom) | Details |
| Regulatory Affairs Manager – London
Introduction
Our client is seeking to appoint a new Regulatory Affairs Manager. The Regulatory Affairs Manager will have CTA experience along with line managment experience as this person will be managing a team of 3-5 people. The Regulatory Affairs Manager should have investigational medicinal product (IMP) experience with hands on clinical trials... [Full Details] |
| Salary: Negotiable (55000 - 65000 £) |
| Regulatory And Drug Safety | Any Grade | Regulatory Affairs | London (United Kingdom) | Details |
| Regulatory Affairs CMC Consultant – London
Introduction
Our client is seeking to appoint a new Regulatory Affairs CMC Consultant. The Regulatory Affairs CMC Consultant will support the clients consultancy and outsourcing services for CMC Research and the manufacture of marketed products for the EU.
Client Profile
The client provides consultancy and outsourcing services to a... [Full Details] |
| Salary: Negotiable (35000 - 40000 £) |
| Regulatory And Drug Safety | Any Grade | QA | Buckinghamshire (United Kingdom) | Details |
| Quality Assurance Auditor (GCP) – Buckinghamshire
Introduction
Our client is seeking to appoint a Quality Assurance Auditor (GCP). The Quality Assurance Auditor (GCP) is responsible for the independent planning and conduct of audits of the clinical research activities of the company, business partners and vendors. These audits provide an independent quality assessment to ensure... [Full Details] |
| Salary: Negotiable (30000 - 40000 £) |
| Regulatory And Drug Safety | Any Grade | QA | Hertfordshire (United Kingdom) | Details |
| Qualified Person (QP) - Hertfordshire
Introduction
Our client is seeking to appoint a new Qualified Person (QP). The Qualified Person’s (QP’s) primary accountability will be to ensure that all GMP/GDP activities are compliant, in addition to providing Quality Assurance expertise to both the sales and development divisions.
Client Profile
The client is a globally leading research... [Full Details] |
| Salary: Negotiable |
| Regulatory And Drug Safety | Any Grade | Regulatory Affairs | London (United Kingdom) | Details |
| Head of EU Regulatory Affairs – London
Introduction
Our client is seeking to appoint a Head of EU Regulatory Affairs. The Head of EU Regulatory Affairs will report to the Vice-President Global Regulatory Affairs based in the US.
The Head of EU Regulatory Affairs is a key position within the European organisation and will provide oversight for EU Regulatory Affairs strategies and... [Full Details] |
| Salary: Negotiable (134000 - 135000 £) |
| Licensing & Contracts | Any Grade | Business Development | Any Location (Singapore) | Details |
| My client is a multinational well-established company with offices around the globe. They are leader in their domain and are currently looking for a Key Account Director to develop their sales in China.
This exciting new opportunity will entail the following responsibilities:
1. Deliver sales of key accounts and markets to meet or exceed target.
2. Plan and deliver key account business... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Any Grade | Any Discipline | Any Location (Czech Republic, Germany,... | Details |
| Leading international CRO, flagman on clinical research market has fantastic position for experienced CRA.
This is permanent position, can be office or home based depending on location.
It is unique opportunity as it will provide with expanded functionality and independent working environment, also it will give experience in innovative enrolment system.
Company offers: ongoing training,... [Full Details] |
| Salary: Negotiable (28000 - 40000 €) |
| CRM (Clinical Research Management) | Any Grade | CRM | Any Location (Germany) | Details |
| My client is a leading Medical Device company and has is currently expanding their Clinical Research team due to their unprecedented success through the recession.
You're responsibilities
Responsible for the design, implementation and initiate of Clinical trials
Must be able to ensure study protocols are compliant with standards set
responsible fir the affective site control and... [Full Details] |
| Salary: Negotiable (100000 - 125000 €) |
| CRM (Clinical Research Management) | Any Grade | CRM | Any Location (Switzerland) | Details |
| My client is a leading Medical Device company and has is currently expanding their Clinical Research team due to their unprecedented success through the recession.
You're responsibilities
Responsible for the design, implementation and initiate of Clinical trials
Must be able to ensure study protocols are compliant with standards set
responsible fir the affective site control and... [Full Details] |
| Salary: Negotiable (130000 - 170000 Other) |
| Clinical Research | Any Grade | CRA | Any Location (Switzerland) | Details |
| My client is a top Device company that specialises in Cardiovascular products. Due to the success in 2010 they are now looking to add to their Clinical Research team
You’re Responsibilities
Managing all aspects of clinical trials ensuring patient safety, compliance with regulations and quality of the data.
Conducting monitoring visits at various sites
Assist on site qualification,... [Full Details] |
| Salary: Negotiable (40000 - 50000 €) |
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