Clinical Research Associate – Multi-Sponsor

🕒 Yesterday

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Perform site qualification, site initiation, interim monitoring, site management activities and close-out visits, on-site or remotely • Evaluate site and site staff performance and provide recommendations regarding site-specific actions • Communicate and escalate serious issues to the project team and develop action plans • Verify informed consent processes and documentation • Assess subject/patient safety, clinical data integrity, protocol deviations/violations and pharmacovigilance issues • Assess site processes and conduct source document review of site source documents and medical records • Verify clinical data entered in case report forms is accurate and complete • Resolve queries remotely and on site and guide site staff toward closure • Use hardware and software for clinical study data review and capture • Verify compliance with electronic data capture requirements • Perform investigational product inventory, reconciliation and storage/security reviews as needed • Verify investigational product dispensing and administration according to protocol • Review Investigator Site Files and reconcile them with the Trial Master File • Document activities through letters, trip reports, communication logs and other project documents • Support subject/patient recruitment, retention and awareness strategies • Track observations, ongoing status and action items to resolution • Manage site-level activities and communications to meet project objectives, deliverables and timelines • Act as primary liaison with study site personnel or collaborate with the Central Monitoring Associate • Train assigned sites and project-specific site team members • Prepare for and attend Investigator Meetings and sponsor face-to-face meetings • Participate in global clinical monitoring/project staff meetings and clinical training sessions • Support audit readiness, audit preparation and follow-up actions

🎯 Requirements

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience • Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements • Good computer skills and ability to embrace new technologies • Excellent communication, presentation and interpersonal skills • Ability to manage required travel of up to 75% on a regular basis • Working knowledge of relevant regulations and company SOPs/processes • Ability to comply with clinical protocols, regulatory requirements, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) • Ability to complete assigned training as required

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations, when appropriate, to assist employees or applicants to perform essential job functions