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| Job Field | Discipline | Region | Actions |
| Clinical Research | Clinical Study Admin | Buckinghamshire (United Kingdom) | Details |
| ----Company:
Our clients develop and market innovative, high-quality pharmaceutical products and services aimed at improving quality of life for people with medical needs across the world. This company aims to reach its values through organisational excellence, commitment to a high-performing culture, advanced medical education approaches, a decentralised structure, and strong customer... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Any Location (Switzerland) | Details |
| Principal Accountabilities and Responsibilities:
•Provides direction and leadership to one or more clinical operations teams
-Builds effective high performing operations teams through integration, motivation and optimising team performance.
-Ensures that each operations team member is aware of their specific area of responsibility, contribution to, and participation in, the operations... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Any Location (Germany) | Details |
| TITLE Associate Clinical Study Director
Based in South and West Germany
£ Excellent Rate + Benefits
Job Summary:
The world's leading pharmaceutical services company is looking for experienced and highly motivated Clinical Research Professionals with a proven track record in study management, who possess well developed communications skills, and who will enjoy working with teams both... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Any Location (Germany) | Details |
| TITLE Project Manager, Clinical Research
Based in Middle-, or West-Germany
Job Summary:
As Project Manager for the Strategic Research and Medical Safety Department, you will manage regionally-based clinical trials in phases IIIb and IV that are ful service in nature, ensuring that all project work is completed to the Sponsor's satisfaction, ensuring quality deliverables on time and within... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Hertfordshire (United Kingdom) | Details |
| Candidates with extensive project management and leadership experience are being sought by one of the largest employers of clinical research and medical sales professionals. This company, that offers the widest range of opportunities in the industry, is seeking 2 Global Studies Leaders on behalf of a top global Pharma, to work with its global Pharma Development Operations team at its office in... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Any Location (Switzerland) | Details |
| Requirements:
1.educated to a life science degree,
2.5 years of experience in clinical research and project management,
3. experience in execution of clinical trials within the budget and timescale.
4.You will also show excellent team leadership skills, and people management skills.
Responsibilities:
1.overall execution of clinical research activities in accordance with the... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | Berkshire, Hampshire, London - Central, Oxfordshire,... | Details |
| A FANTASTIC OPPORTUNITY TO WORK WITH A FAST GROWING MEDIUM SIZED GLOBAL PHARMACEUTICAL COMPANY AS A SCRA / JUNIOR PROJECT MANAGEMENT ROLE. THIS POSITION WILL ALLOW YOU TO STEP AWAY FROM MONITORING TO WORK CLOSELY WITH CRO'S IN DELIVERING PROJECTS
The role of a Senior CRA (SCRA) is to take a leadership role in overseeing specific aspects of individual clinical studies, working under the... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | Berkshire, Hampshire, Surrey, London - South (United... | Details |
| Senior Clinical Research Associate
Our client currently is a world leader in the field of biotechnology, developing products with the highest standards of quality, safety and efficacy for the benefit of their patients. Currently they are looking for a Senior Clinical Research Associate to work in their offices in the South East. The role presents an excellent opportunity to work in an... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | Bedfordshire, Cambridgeshire, Essex, Hertfordshire,... | Details |
| This organisation is one of the Global Leaders in Biotechnology. With operations in over 30 counties and leading edge research in Oncology there is huge potential for career development and growth. This is reflected in this organisations inclusion in ‘best 100’ employers rating as one of the best corporate employers in the UK.
Clinical Trial Administrator - Biotech - Cambridge
You will... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | Berkshire, Buckinghamshire, Gloucestershire, Oxfordshire... | Details |
| We are currently seeking an experienced (Senior) Clinical Research Associate who is looking to progress their career and develop more skills. If you are looking for an opportunity to move forward then this is the right opportunity for you! In addition to their very competitve salary, they offer a fantastic benefits package with relocation assistance where appropriate!
Position... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Hampshire (United Kingdom) | Details |
| There are excellent opportunities for experienced clinical research professionals to take clinical project management roles for one of the largest employers of clinical research and medical sales professionals, that offers the widest range of opportunities in the industry. They are seeking 2 Clinical Project Managers to work with a top global Pharma, in the Oncology or CNS therapeutic area, at... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | Any Location (Switzerland) | Details |
| Duties:
Act as a liaison between the company and investigator sites.
participate in Study Team meetings and write minutes
Review clinical study documents for accuracy and completeness of questionnaires, approvals and renewals, IRB membership lists and assurance numbers, ICFs,
advertisements, protocols, and amendments, laboratory certifications and lab values, and review study... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Any Location (Germany) | Details |
| Duties:
•Provides input to clinical study design and protocol
•Coordination of operational and logistical tasks related to international phase I-III vaccine clinical trials according to ICH-GCP guidelines and national and international regulations
•Acting as the primary contact to the associated CRO Project Manager and Clinical Study Investigators
•Submission of documents to and... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | Any Location (United Kingdom) | Details |
| Leading a group of study managers and CTAs, the senior study manager is responsible for delivering the operational aspects of one or more clinical studies from protocol feasibility through database release. Their primary deliverable is high-quality, timely and cost-effective data. The senior study manager also contributes beyond database release to support effective study reporting and... [Full Details] |
| Salary: Negotiable (50000 - 55000 £) |
| CRM (Clinical Research Management) | Clinical Study Admin | Any Location (Germany) | Details |
| In this position you are responsible for
•Preparation/coordination of international clinical trials phase I-IV
•Leading an international, multi-disciplinary study team
•Planning, tracking and controlling the study budget and study timelines
•Manage risk assessment and mitigation plans
•Leading the site selection, feasibility and trial submission process of international clinical... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Any Location (United Kingdom) | Details |
| The Clinical Programme Scientist is a key role for a world class pharmaceutical company that develops safe, effective and innovative pharmaceutical products and now ranks as the fastest-growing among the UK's top 50 pharmaceutical companies. The successful candidate will be based in the company's office in the south-east of England and will represent clinical science on the regional (US/EU)... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Berkshire (United Kingdom) | Details |
| This exciting and challenging role is with a leading global CRO that has a record of phenomenal success in the market place. The company has helped to develop or commercialise every single one of the world's top 30 selling drugs and their Study Start-Up Group ensures fast patient recruitment and start-up for both local studies and complex multi-site, multinational studies. They require an... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | Any Location (Spain) | Details |
| Participación del diseño de protocolos de ensayos clínicos y análisis e interpretación estadística de los datos generados.
Formación y Experiencia:
Formación específica:
• Diplomatura en Estadística. Deseable Licenciatura en Matemáticas. Se considerarán candidaturas de Licenciados en Ciencias de la Salud con experiencia en Clinical Research y experiencia en biometría.
• Conocimientos... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | Buckinghamshire (United Kingdom) | Details |
| ----Company:
With over 50 years of health care experience, our client has earned a reputation as an innovative leader in pharmaceutical and health care research and development.
By devoting a significant portion of their revenues to research and development, this company seeks to use proprietary technology to develop unique pharmaceutical products that create value and achieve a... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Berkshire (United Kingdom) | Details |
| Perm: Berkshire Office Based, Associate Director of Clinical Site Start-Up Group – Line Management
Contact Information:
Lee Dunn
Tel: +44 (0) 207 255 6665
Lee.dunn@1st-pharmapeople.com
http://www.1st-pharmapeople.com
Job Summary:
In this role you will be charged to: Develop and implement department procedures and manage overall team activities. Assist with the formulation,... [Full Details] |
| Salary: 55000 - 62000 £ |
| CRM (Clinical Research Management) | Clinical Study Admin | Berkshire (United Kingdom) | Details |
| Perm: Berkshire Office Based, Line Manager of Clinical Site Start-Up Group – 50+ Associates
Contact Information:
Lee Dunn
Tel: +44 (0) 207 255 6665
Lee.dunn@1st-pharmapeople.com
http://www.1st-pharmapeople.com
Job Summary:
The purpose of this role is to Line Manage the Site Start-Up Group of over 50 associates that ensures fast patient recruitment and start-up for both local... [Full Details] |
| Salary: 40000 - 50000 £ |
| Clinical Research | Clinical Study Admin | Cambridgeshire (United Kingdom) | Details |
| Job Title: Contracts Co-ordinator
Location: Cambridgeshire
We are assisting one of our clients in finding a Contracts Co-ordinator for their office in Cambridge.
The basic purpose of this position is to support all activities of the Contracts team. The Contracts Co-ordinator will work with Contracts team to assist in the completion and execution of contracts with clinical study sites... [Full Details] |
| Salary: Negotiable |
| Clinical Research | Clinical Study Admin | West Lothian (United Kingdom) | Details |
| SUMMARY
Our client, a CRO focused on streamlining and supporting the drug development process for biotechnology and pharmaceutical innovators, currently have an exciting opportunity for a Quality Associate to join the GMP Quality team on a Temporary Maternity Cover basis.
In return our client offers a challenging position with attractive salary within a world leading... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Kent (United Kingdom) | Details |
| An experienced Project Planner is needed by early June for an office based, 6 month contract role with one of the world's premier research-based pharmaceutical companies, that discovers, develops, manufactures and markets a wide range of innovative, pharmaceutical products for humans and animals around the world. The successful candidate, who will ideally come from a pharmaceutical background,... [Full Details] |
| Salary: Negotiable |
| CRM (Clinical Research Management) | Clinical Study Admin | Cambridgeshire (United Kingdom) | Details |
| A Bio-Pharmaceutical company is currently seeking a full time Clinical Project Manager to join their thriving team in Cambridgeshire. You will be responsible for managing the clinical trials within program budgets and timelines demonstrating your ability to deliver results under deadlines and enjoy working in a fast paced environment. You will be working within the therapeutic areas of... [Full Details] |
| Salary: Negotiable |
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