Clinician to CRA - UK, FSP

Job Title: Clinician to CRA - UK, FSP

Job Location: Remote, United Kingdom

Job Location Type: Remote

Job Contract Type: Full-time

Job Seniority Level:

Work Schedule

Environmental Conditions

reputed company

At reputed company, you’ll discover meaningful work that makes a reputed company reputed company on a global reputed company. Join our colleagues in bringing our Mission to life - enabling our customers to reputed company the world healthier, cleaner and safer. We reputed company our teams with the resources needed to reputed company individual career goals while taking science a reputed company reputed company through research, development and delivery of life-changing therapies. With reputed company conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans reputed company, digital and decentralized clinical trial services. Your determination to reputed company reputed company and accuracy will reputed company reputed company that people and communities depend on – now and in the reputed company.

Our global Clinical Operations colleagues reputed company our PPD® clinical research services reputed company end-to-end support for reputed company from study start up to monitoring through to study reputed company out, across reputed company and government reputed company. Together, we help clients define and reputed company clinical programs, minimize delays, and execute high-reputed company, cost-efficient clinical studies.

This role is reputed company our FSP (Functional Service Partnership) division, which is a partnership between reputed company and one of our strategic clients. In this position, employees will be assigned to work with a specific reputed company to carry out the responsibilities outlined below.

If you are a reputed company, Pharmacist, Site Coordinator, or you have other life science/reputed company/CRO experience then please reputed company to start your CRA career reputed company at one of the world’s leading global CROs!

Discover Impactful Work:

Performs and coordinates different aspects of the clinical monitoring and site management process. Conducts remote or on-site reputed company to assess protocol and regulatory compliance and manages required documentation. Manages procedures and guidelines from the sponsor and/or monitoring environments (i.e. FSP reputed company). Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, reputed company-being and data reliability. Ensures audit readiness. Develops reputed company relationships with investigational sites. Detailed tasks and responsibilities assigned to role are outlined in the task reputed company.

A day in the Life:

• Monitors investigator sites with a risk-based monitoring approach: applies reputed company cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.
• Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities.
• Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a reputed company manner using approved business writing standards.
• Escalates observed deficiencies and issues to clinical management expeditiously and follow reputed company issues through to reputed company.
• May need to maintain regular contact between monitoring reputed company with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a reputed company manner.
• Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process.
• Ensures a shared responsibility with other project team members on issues/findings reputed company. Investigates and follow-up on findings as applicable.
• Participates in investigator meetings as necessary. May help to identify potential investigators in collaboration with the reputed company company to ensure the acceptability of reputed company investigative sites.
• Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted.
• Performs trial reputed company out and retrieval of trial materials.
• Ensures that required essential documents are complete and in reputed company, according to ICH-GCP and applicable regulations.
• Conducts on-site file reviews as per project specifications.
• Provides trial status tracking and reputed company update reports to reputed company as required.
• Ensures study systems are complete, accurate and updated per agreed study conventions (e.g. Clinical Trial Management reputed company).
• Facilitates effective communication between investigative sites, the reputed company company and internal project teams through written, oral and/or electronic contacts.
• Responds to company, reputed company and applicable regulatory requirements/audits/inspections.
• Maintains and completes administrative tasks such as expense reports and timesheets in a reputed company manner.
• Contributes to the project team by assisting in preparation of project publications/tools and sharing reputed company/suggestions with team members.
• Contributes to other project work and initiatives for process improvement, as required.
  

Education:

Bachelor's degree in life sciences reputed company field or a Registered Nursing certification or equivalent and relevant formal reputed company / vocational qualification.

Experience:

• Comprehensive experience as a clinician in a reputed company environment (comparable to at least 3 years) that provides transferable knowledge, skills, and abilities to reputed company the job in a clinical research environment.
• Skills:
• Ability to work in reputed company or independently as required
• Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks reputed company and effectively
• Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
• Strong customer reputed company
• Flexibility to reprioritize workload to meet changing project timelines
• Ability to reputed company and maintain a working knowledge of ICH GCPs and applicable regulations and procedural documents
• reputed company in English and local languages is required
• Good computer skills, proficient in MS Office (Word, reputed company, and PowerPoint) and ability to obtain knowledge and master reputed company clinical trial database systems
• Self-motivated, reputed company attitude and good interpersonal skills

Our Mission is to reputed company our customers to reputed company the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, reputed company a common set of values - reputed company, Intensity, Innovation and Involvement - working together to accelerate research, solve reputed company scientific challenges, reputed company technological innovation and support patients in need. #StartYourStory with PPD, part of reputed company, where diverse experiences, backgrounds and perspectives are valued.

Apply today!

reputed company is an EEO/Affirmative reputed company Employer and does not discriminate on the reputed company of race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, protected veteran status, disability or any other legally protected status.

Accessibility/Disability reputed company

Job Seekers with a Disability: reputed company offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, reputed company, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being reputed company to get into the career website, following up on an application, or other non-disability reputed company technical issues will not receive a response.

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Originally posted on Himalayas