Senior Clinical Research Associate
ICON
CRA II/Sr. CRA- Detroit, MIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.Collaborating with investigators and site staff to facilitate smooth study conduct.Performing data review and resolution of queries to maintain high-quality clinical data.Contributing to the preparation and review of study documentation, including protocols and clinical study reportsYour Profile:You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:Bachelor's degree in a scientific or healthcare-related field.Minimum of 2 years of experience as a Clinical Research Associate.In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.Strong organizational and communication skills, with attention to detail.Ability to work independently and collaboratively in a fast-paced environment.Willingness to travel as required (approximately 60%)Employment with ICON is contingent upon having the legal right to work in the country where the role is based.Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.Benefits may include:Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Inclusion and AccessibilityICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
$96.2k - $151.4k
...primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.... ...Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.Gains an in-depth understanding of the study protocol...SuggestedFull timeFor contractorsLocal areaRemote workFlexible hours2 days per week3 days per week- ...Equity/Stock option program, and additional bonus opportunities.Medpace is growing quickly and we are seeking Experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented, mid-sized CRO focused on full-service project work....SuggestedContract workWork at officeRemote workWork from home
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...Intelligence Platform with Slalom’s broader consulting, engineering, industry, and delivery capabilities. This role is ideal for a senior technical leader who can move comfortably between executive conversations, solution architecture, partner strategy, and hands-on technical...SeniorTemporary workLocal area- Clinical Research Associate - Oncology - Detroit, MI ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission...Remote jobLocal areaVisa sponsorshipFlexible hours
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$80k - $105k
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