HavenEngland
Join our team at Golden Sands set in the beautiful town of Rhyl with a gorgeous beach setting and lots of Haven fun.Quebec Road, Mablethorpe, Lincs LN12 1QJ GBR.Come andjoin our One Great Team here at Haven as a Fast Food Shift Leader!.Who doesn’t love a good takeaway? .At Haven, we’ve brought some ...
Hays Accountancy and FinanceOxford
Competitive, DOE + Study Support.Our client is a leading independent Oxford accountancy practice who are actively recruiting for new trainee accountants!.From preparing a set of accounts for a sole trader one week, you could be a member of a team auditing the accounts of a large group of companies t...
Cornerstone HealthcareHam, 21 mi from Didcot
About The Role
Check below to see if you have what is needed for this opportunity, and if so, make an application asap.
We are looking for a highly experienced and dedicated Clinical Manager with a background in nursing and complex care. You...
Wantage, 7 mi from Didcot
of the year. If you would like to work for a multi award winning care provider who supports its managers to achieve their ambitions then apply today for a confidential conversation. Deputy Manager Clinical
Please ensure you read the below overview...
FinegreenOxford, 9 mi from Didcot
We are working with an NHS organisation who are seeking to appoint an Interim Clinical Services Manager for CAMHS. This role will start ASAP and will be for 6 months initially.
The role will be at band 8a under the AfC NHSI Agency Capped rates...
Leaders in CareEaling, 38 mi from Didcot
Are you a dedicated, ambitious and seasoned Clinical Manager? If so, we've got an exciting role for you. Our client is a well-established hospital in Ealing, offering personalised treatment for service users with an eating disorder or personality...
Leaders In Care Recruitment LtdEaling, 38 mi from Didcot
Are you a dedicated, ambitious and seasoned Clinical Manager? If so, we've got an exciting role for you. Our client is a well-established hospital in Ealing, offering personalised treatment for service users with an eating disorder or personality...
Nurse SeekersOxford, 9 mi from Didcot
Clinician Liaison Manager
Nurse Seekers are proud to be working alongside a market leading Dermatology company and assisting in their search for a Clinician Liaison Manager
The Role: The Clinician Liaison Manager plays a pivotal role in attracting...
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Clinical Research Associate
Didcot | www.cv-library.co.uk |
Cure Talent are delighted to be partnered with an established Medical Devices Manufacturer, who, due to their continued growth, have an exciting opportunity for an experienced Clinical Research to join them.
As the new Clinical Research Associate, you will be responsible for overseeing trial sites, managing trial data, ensuring compliance with regulatory requirements and maintaining the integrity of study protocols.
This is a remote position with occasional site visits.
We are looking for an experienced clinical research professional with proven experience in clinical trial management, preferably from Medical Devices. Proficiency in regulatory requirements, GCP guidelines, and clinical trial data management systems is essential for success in this role.
Key Responsibilities:
• Manage the data collected during trials, overseeing trial sites, and conducting regular in-person or virtual site visits.
• Collaborate with sponsors at trial sites to ensure ethical conduct and adherence to regulations and guidelines.
• Ensure compliance with protocols, standard operating procedures, and Good Clinical Practice (GCP) guidelines.
• Review and analyse clinical trial data for accuracy and completeness.
• Develop and maintain study timelines and budgets.
Skills & Qualifications:
• Degree educated in a relevant discipline.
• Proven experience in a Clinical Research/Clinical Trial Management position
• Knowledge of regulatory requirements and guidelines, including GCP and ICH.
• Familiarity with clinical trial data management systems and electronic data capture.
• Experience with site selection, initiation, management, and monitoring activities.
Desirable Skills & Qualifications:
• Certification in clinical research, such as ACRP certification.
• Understanding of medical device regulation and development processes.
• Working knowledge of medical terminology and anatomy.
• Excellent project management and leadership skills.
• Ability to work collaboratively with study teams and cross-functional departments.
If you have the necessary skills and experience to be successful in this role, please get in touch with the team at Cure Talent today
As the new Clinical Research Associate, you will be responsible for overseeing trial sites, managing trial data, ensuring compliance with regulatory requirements and maintaining the integrity of study protocols.
This is a remote position with occasional site visits.
We are looking for an experienced clinical research professional with proven experience in clinical trial management, preferably from Medical Devices. Proficiency in regulatory requirements, GCP guidelines, and clinical trial data management systems is essential for success in this role.
Key Responsibilities:
• Manage the data collected during trials, overseeing trial sites, and conducting regular in-person or virtual site visits.
• Collaborate with sponsors at trial sites to ensure ethical conduct and adherence to regulations and guidelines.
• Ensure compliance with protocols, standard operating procedures, and Good Clinical Practice (GCP) guidelines.
• Review and analyse clinical trial data for accuracy and completeness.
• Develop and maintain study timelines and budgets.
Skills & Qualifications:
• Degree educated in a relevant discipline.
• Proven experience in a Clinical Research/Clinical Trial Management position
• Knowledge of regulatory requirements and guidelines, including GCP and ICH.
• Familiarity with clinical trial data management systems and electronic data capture.
• Experience with site selection, initiation, management, and monitoring activities.
Desirable Skills & Qualifications:
• Certification in clinical research, such as ACRP certification.
• Understanding of medical device regulation and development processes.
• Working knowledge of medical terminology and anatomy.
• Excellent project management and leadership skills.
• Ability to work collaboratively with study teams and cross-functional departments.
If you have the necessary skills and experience to be successful in this role, please get in touch with the team at Cure Talent today
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