Regulatory Efficacy Specialist

REF: - INTERCONNECTEMEA00285- DIVISION: - Smiths Interconnect- JOB FUNCTION: - Legal and ComplianceAbout us - Employing over 2,000 people globally our in house capabilities encompass design, development, manufacturing and testing to respond quickly and accurately to customer's needs and provide the most reliable connectivity solutions.We have a fantastic...

Overview: Work as a statistician on clinical trials; producing and validating complex outputs to excellent quality whilst adhering to deliverable timelines. Producing and reviewing Statistical Analysis Plans (SAPs), protocols and other pertinent study documentation. Acting as lead statistician within a reporting team environment, being responsible for...

**Biostatistician - Contract - 6 months initial contract - Hybrid/Netherlands** We are a prestigious Life Sciences Consultancy with a powerful and successful consultancy base, seeking for a highly skilled and experienced biostatistician to join our team as a contractor. The contractor statistician will be responsible for providing statistical support for...

Overview: **THE COMPANY** Phastar is a multiple award-winning global biometric Contract Research Organization (CRO) that is accredited as an outstanding company to work for by Best Companies. We partner with pharmaceutical, biotechnology and medical device organizations to provide the expertise and processes to manage and deliver on time, quality...

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...

**Job Overview** Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. **_At least 3 years' experience with submissions....

IQVIA Biotech is looking for an experienced Clinical Study Start-up professional in the UK to join our Study Start-Up Unit. The Study Start-up Specialists are responsible for conducting and facilitating specific start-up activities that may include site identification, feasibility, essential document collection and review, ICF customization, EC and CA...

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...

Job Advert **Quantuma, part of the K3 Capital Group is an independent advisory firm serving the needs of mid-market and corporate companies, as well as their stakeholders. Our experts advise clients on business transactions, resolving business disputes, mitigating risk and managing operational as well as financial challenges. We have deep experience and...

Sr Country Approval Specialist (Study Start-up / Submissions Specialist) At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to...

Sr Country Approval Specialist (Study Start-up / Submissions Specialist) At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to...

About the Role:As a Medical Affairs Advisor at CK Group, you will play a vital role in providing medical and scientific advice to healthcare professionals. This contract-based position offers an exciting opportunity to work in the pharmaceutical industry and contribute to the discovery, development, and provision of medicines.Responsibilities:Provide...

We are currently seeking a highly motivated and skilled individual to join our team as a Medical Scientific Liaison Specialist II at Thermo Fisher Scientific Inc. in the United Kingdom, covering the midlands and Wales. This position offers an exceptional opportunity to showcase your expertise and contribute to our world-class organization. - Job...

**Desktop Environment Specialist** Leatherhead, Surrey (Hybrid model) - Competitive salary between £37,000 up to £38,000, depending on experience - A workplace pension scheme - Hybrid working - 25 days’ annual leave with options to purchase and sell holiday (excluding Bank Holidays) - Support and investment in your personal development - 24/7 access to...

**Operational Excellence & Change Specialist - ARDGA841881 - Home/National** We have an exciting opportunity to join our team, reporting to the Regional Operations Director and working remotely you will be responsible for Business Improvement and Project Support. Our Operational Excellence & Change Specialist is responsible for providing support to drive,...

Job Title: Pharmaceutical Compliance SpecialistWe are seeking a highly experienced Pharmaceutical Compliance Specialist to join our dynamic team. This is an exciting opportunity to play a crucial role in ensuring compliance with regulatory requirements while leveraging data and AI in the development of life-changing therapies.Key Responsibilities:Provide...

Belmont Green- Remote- Role Purpose The Collections & Recoveries Specialist is responsible for ensuring mortgage customers receive fair outcomes, in line with agreed processes, company policies and industry regulation. The main responsibilities of the role are to ensure BGFL has effective oversight of collections and recoveries activities carried out by our...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners...

OverviewTechNET-IT is working with a leading organisation in the global pharmaceutical and biotechnology industry to find a Senior Data Compliance Specialist, Data & AI. This role plays a crucial part in ensuring compliance with regulatory requirements while leveraging data and AI in the development of life-changing therapies.

**Operational Change Specialist - ARDGA841881 - Remote** We have an exciting opportunity to join our team, reporting to the Regional Operations Director you will support the Division with any operational change needed that impacts the business. Our Operational Change Specialist will work with the business to ensure operational change is delivered...