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Clinical Researcher 1
| Dyddiad hysbysebu: | 09 Chwefror 2025 |
|---|---|
| Cyflog: | £38,044.37 bob blwyddyn |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 02 Mawrth 2025 |
| Lleoliad: | UK |
| Gweithio o bell: | Yn gyfan gwbl o bell |
| Cwmni: | Snooze Science LTD |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: |
Crynodeb
About Us: Snooze Science is dedicated to improving sleep health through innovative technology and evidence-based solutions.
At Snooze Science, we are dedicated to providing high-quality medical services to our patients. Our mission is to improve the health and well-being of our community through compassionate care and personalized treatment plans.
We are looking for a passionate Clinical Researcher to join our team and contribute to our mission of enhancing sleep quality for our users.
Job Summary:
A Clinical Researcher is responsible for designing, conducting, and overseeing clinical trials to test the safety and efficacy of treatments. This role involves collaborating with a team of scientists and regulatory agencies to ensure the successful execution of clinical studies.
Key Responsibilities:
Design and Develop Protocols: Create detailed plans for clinical trials, including objectives, methodologies and timelines.
Collaborate with cross-functional teams to design clinical studies focused on sleep health
Ensure compliance with ethical standards and regulatory requirements.
File all original documents for study in TMF (Trial Master File)
Recruit Participants: Identify and screen potential participants for clinic trials, ensuring they meet the study criteria.
Participant Recruitment and Screening: Identify and recruit study participants through various channels.
Conduct initial screenings and obtain informed consent from participants.
Maintain accurate records of participant information and study progress.
Patient Interaction: Monitor and support participants throughout the trial,
Addressing any issues or concerns that arise.
In collaboration with Data Scientist-Data Collection strategies and Analysis:
Collect, manage, and analyse data from clinical trials to assess the safety and
effectiveness of the interventions
Regulatory Compliance: Ensure all clinical trials comply with local, national,
and international regulations and ethical standards.
Collaboration: Work closely with other researchers, physicians, and regulatory
bodies to coordinate and conduct trials.
Reporting: Prepare detailed reports and presentations on the findings of clinical
trials for stakeholders and publication in scientific journals by Supporting
and collaborating physicians etc in Publication and dissemination:
Write and submit research papers to peer-reviewed journals.
Present findings at conferences and industry events.
Collaborate with the marketing team to communicate research insights to the Public
Continuous Improvement
Stay updated with the latest research and advancements in sleep science.
Provide feedback to the product development team to enhance app features based on research findings.
Participate in ongoing training and professional development opportunities.
Required Skills and Qualifications:
Educational Background: A degree in a relevant field such as biology, chemistry, medicine, or a related discipline. Master's or Advanced degrees (e.g., Ph.D.) are a plus.
Strong understanding of sleep science and related health issues.
Experience: Previous experience in clinical research or a related field is highly desirable.
Technical Skills: Proficiency in data analysis software and clinical trial management systems.
Attention to Detail: Strong observational skills to accurately track and record data.
Communication Skills: Excellent verbal and written communication skills for interacting with participants, colleagues, and stakeholders.
Organizational Skills: Ability to manage multiple tasks and projects simultaneously.
Ethical Standards: Commitment to maintaining high ethical standards and ensuring patient safety.- Ability to work independently and as part of a team.
At Snooze Science, we are dedicated to providing high-quality medical services to our patients. Our mission is to improve the health and well-being of our community through compassionate care and personalized treatment plans.
We are looking for a passionate Clinical Researcher to join our team and contribute to our mission of enhancing sleep quality for our users.
Job Summary:
A Clinical Researcher is responsible for designing, conducting, and overseeing clinical trials to test the safety and efficacy of treatments. This role involves collaborating with a team of scientists and regulatory agencies to ensure the successful execution of clinical studies.
Key Responsibilities:
Design and Develop Protocols: Create detailed plans for clinical trials, including objectives, methodologies and timelines.
Collaborate with cross-functional teams to design clinical studies focused on sleep health
Ensure compliance with ethical standards and regulatory requirements.
File all original documents for study in TMF (Trial Master File)
Recruit Participants: Identify and screen potential participants for clinic trials, ensuring they meet the study criteria.
Participant Recruitment and Screening: Identify and recruit study participants through various channels.
Conduct initial screenings and obtain informed consent from participants.
Maintain accurate records of participant information and study progress.
Patient Interaction: Monitor and support participants throughout the trial,
Addressing any issues or concerns that arise.
In collaboration with Data Scientist-Data Collection strategies and Analysis:
Collect, manage, and analyse data from clinical trials to assess the safety and
effectiveness of the interventions
Regulatory Compliance: Ensure all clinical trials comply with local, national,
and international regulations and ethical standards.
Collaboration: Work closely with other researchers, physicians, and regulatory
bodies to coordinate and conduct trials.
Reporting: Prepare detailed reports and presentations on the findings of clinical
trials for stakeholders and publication in scientific journals by Supporting
and collaborating physicians etc in Publication and dissemination:
Write and submit research papers to peer-reviewed journals.
Present findings at conferences and industry events.
Collaborate with the marketing team to communicate research insights to the Public
Continuous Improvement
Stay updated with the latest research and advancements in sleep science.
Provide feedback to the product development team to enhance app features based on research findings.
Participate in ongoing training and professional development opportunities.
Required Skills and Qualifications:
Educational Background: A degree in a relevant field such as biology, chemistry, medicine, or a related discipline. Master's or Advanced degrees (e.g., Ph.D.) are a plus.
Strong understanding of sleep science and related health issues.
Experience: Previous experience in clinical research or a related field is highly desirable.
Technical Skills: Proficiency in data analysis software and clinical trial management systems.
Attention to Detail: Strong observational skills to accurately track and record data.
Communication Skills: Excellent verbal and written communication skills for interacting with participants, colleagues, and stakeholders.
Organizational Skills: Ability to manage multiple tasks and projects simultaneously.
Ethical Standards: Commitment to maintaining high ethical standards and ensuring patient safety.- Ability to work independently and as part of a team.