Clinical Trials Recruitment Coordinator
4 days ago
**Company Overview**
Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients.
As a growing and successful business, we employ more than 1,300 talented individuals globally, located at state-of-the-art development, manufacturing and clinical facilities in the UK and USA.
Science, Agility and Culture are the core components that define Quotient Sciences, enabling us to do what we do in the way that we do it. People join Quotient Sciences because we are a respected member of the drug development community, driven by an unswerving belief that ideas need to become solutions, and molecules need to become cures, fast. Because humanity needs solutions, fast.
**The Role**
We have an excellent career opportunity for a Clinical Trials Recruitment Coordinator, recruiting volunteers for Clinical Trials
Join our Volunteer Management team as a Clinical Trials Recruitment Coordinator. In this role you will provide administrative and recruitment support in all aspects of volunteer recruitment into our clinical trials.
**Other tasks and responsibilities include**:
- Production and distribution of detailed trial information to volunteers
- Working outside of core hours when necessary
- Attending study and departmental meetings
- Archiving study information as appropriate
- Quality checking and preparation of volunteer files and general administrative support as required.
- Organising appointments and ensure that all the paperwork is completed correctly in good time for the start of the trial.
- Calculation and organisation of payments to volunteers
- Preparation of metrics
- Maintaining accurate data on the database is critical throughout this process, so ideally you’ll have experience of dealing with a database in a previous job.
**Other skills and experience required**:
- Previous administrative experience would be desirable
- Able to prioritise own and others workloads
- Proficiency in accurately maintaining databases
- Excellent written and oral communication skills
- Impeccable telephone manner
- Multitasking skills
- Proactive approach to overcoming challenges
- Full training will be provided
**Company benefits**
In return, you will receive a competitive salary, benefits package, excellent training and development, as well as an exciting career within a fast paced and dynamic business.
**Our Commitment to Diversity & Inclusion**
Quotient Sciences are advocates for positive change and conscious inclusion.
We strive to create a diverse Quotient family by remaining committed to the development of our culture, equality, mindset, diversity & inclusion in the workplace.
As a global employer, we recognise the value in having an organisation that is a true reflection and representation of our society today. All applicants welcome.
-
Global Clinical Trial Coordinator
2 weeks ago
Nottingham, Nottingham, United Kingdom Advanced Clinical Full timeJob Requirements: Experienced Clinical Trials ProfessionalEstimated Salary: $140,000 per annumThe Senior Clinical Trial Manager is an experienced professional with a strong background in clinical trials operations. This individual will oversee clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good...
-
Clinical Trials Associate
2 days ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number**4540** **Employment Type**:Regular** **The Clinical Trials Associate is responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.** **RESPONSIBILITIES**: - Tasks may include but are...
-
Clinical Trials Document Manager
1 month ago
Nottingham, Nottingham, United Kingdom Worldwide Clinical Trials Full timeOverview:As a Regulatory Compliance Specialist at Worldwide Clinical Trials, you will play a key role in ensuring the accuracy and completeness of our clinical trial documents. This position requires attention to detail, organizational skills, and excellent communication abilities.About Us:Worldwide Clinical Trials is a global CRO with a strong reputation...
-
Clinical Trial Manager
2 weeks ago
Nottingham, Nottingham, United Kingdom Advanced Clinical Full timeJob Title: Clinical Trial ManagerAbout Advanced Clinical:Advanced Clinical is a leading provider of clinical research services, dedicated to delivering high-quality results and exceeding customer expectations. Our team of experts works tirelessly to ensure that our clients receive the best possible support for their clinical trials.Job Description:We are...
-
Clinical Trials Associate
1 day ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number** **6076** **Employment Type***: **Regular** **Who we are** We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with...
-
Clinical Trials Manager
2 weeks ago
Nottingham, Nottingham, United Kingdom Advanced Clinical Full timeJob DescriptionThe Senior Clinical Trial Manager at Advanced Clinical oversees clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements. This role is an excellent opportunity to work on vendor management and site engagement in LATAM for a Phase III...
-
Clinical Trials Operations Lead
2 weeks ago
Nottingham, Nottingham, United Kingdom Advanced Clinical Full timeJob Title: Clinical Trials Operations LeadLocation: Worldwide (Remote)The Sr Clinical Trial Manager will oversee clinical trial sites from start-up to close-out, ensuring compliance with the study protocol, ICH guidelines, Good Clinical Practices (GCP), and regulatory requirements.This role collaborates with the Clinical Project Manager (CPM), CRO...
-
TMF Quality Control Coordinator
1 month ago
Nottingham, Nottingham, United Kingdom Worldwide Clinical Trials Full timeJoin Our Team:As a Regulatory Compliance Specialist at Worldwide Clinical Trials, you will play a critical role in ensuring the quality and integrity of our clinical trial documents. If you are a detail-oriented professional with a passion for regulatory compliance, we encourage you to apply for this exciting opportunity.About the Role:This position requires...
-
Associate Director, Clinical Data Management
7 months ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number**7869** **Employment Type**:Regular** **Who we are** Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s...
-
Medical Writer
2 days ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number** **6136** **Employment Type***: **Regular** Worldwide is looking for experienced Medical Writers to join our global team! We are a fast-growing organisation, and we are continuously looking for talented people across the globe to become part of our uncommon team! **Who we are** We’re a global, mid-size CRO that pushes boundaries,...
-
Regulatory Compliance Specialist
1 month ago
Nottingham, Nottingham, United Kingdom Worldwide Clinical Trials Full timeJob Summary:We are seeking a highly skilled Regulatory Compliance Specialist to join our team at Worldwide Clinical Trials. In this role, you will be responsible for ensuring the quality and compliance of clinical trial documents.About Us:Worldwide Clinical Trials is a global team of over 3,500 experts who are changing the way the world experiences CROs. We...
-
Associate / Clinical Database Programmer (Sas)
7 months ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number**7609** **Employment Type**:Regular** **Who we are** Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s...
-
Pharmacovigilance Associate
3 days ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number** **6249** **Employment Type***: **Regular** **Who we are** We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with...
-
Clinical Trial Supply Associate
4 days ago
Nottingham, United Kingdom Quotient Sciences Full time**Company Overview** Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients. As a...
-
Senior Pharmacovigilance Associate
7 months ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number** **6982** **Employment Type***: **Regular** **Who we are** We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with...
-
Research Project Coordinator
2 weeks ago
Nottingham, Nottingham, United Kingdom Actalent Full timeAbout the RoleAs a Study Coordinator, you will play a critical role in supporting the success of our clinical trials.With a strong background in clinical research and excellent organizational skills, you will be responsible for ensuring the smooth execution of our studies.Your Key Responsibilities:Managing study documentation and reportsCoordinating with...
-
Clinical Trials Recruitment Administrator
2 days ago
Nottingham, United Kingdom Quotient Sciences Full time**Company Overview** Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we save precious time and money in getting drugs to patients. As a growing and successful business, we...
-
Principal Statistician Eu/usa
7 months ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number** **6981** **Employment Type***: **Regular** **Who we are** We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with...
-
Clinical Trials Volunteer Administrator
4 days ago
Nottingham, United Kingdom Quotient Sciences Full time**Company Overview** Quotient Sciences is a drug development and manufacturing accelerator providing integrated programs and tailored services across the entire development pathway. Cutting through silos across a range of drug development capabilities, we help biotech and pharma customers save precious time and money in getting drugs to patients. As a...
-
Senior Statistician
7 months ago
Nottingham, United Kingdom Worldwide Clinical Trials Full time**Requisition Number**7913** **Employment Type**:Regular** **Who we are** Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications - from discovery to reality. Anchored in our company’s...