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randomisation, data analysis, and results reporting.</li>\n<li>Support the statistical aspects of case report form design.</li>\n<li>Help in writing statistical analysis plans, defining derived data, and designing statistical tables and figures for clinical summary reports.</li>\n<li>Write data quality control specifications, utilise relevant computer languages and software.</li>\n<li>Develop and execute data manipulation and analysis programs.</li>\n<li>Assist in conducting statistical analyses and interpreting results.</li>\n<li>Prepare statistical summary reports and contribute to the statistical methods sections of integrated study reports.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in Statistics or a related field.</li>\n<li>Experience in a biostatistics role in the pharmaceutical, clinical research, or healthcare industry is preferred.</li>\n<li>RWE experience required.</li>\n<li>Proficiency in statistical concepts, study design, sample size calculations, and patient randomisation.</li>\n<li>Familiarity with statistical analysis plans and the design of statistical tables, figures, and data listings for clinical reports.</li>\n<li>Strong data analysis skills, including data manipulation, retrieval, and interpretation.</li>\n<li>Proficiency in relevant computer languages and statistical software packages.</li>\n<li>Ability to write and implement programs to select, retrieve, manipulate, edit, and analyse data.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>","enriched_at":1793009672644},{"id":"job_908c01dc-eb9","title":"Clinical Research Associate","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Portland-OR/CRA_JR161809","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>As a Clinical Research Associate (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.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:</p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li>\n<li>Performing data review and resolution of queries to maintain high-quality clinical data.</li>\n<li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific or healthcare-related field.</li>\n<li>Minimum of 2 years of experience as a Clinical Research Associate.</li>\n<li>In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li>\n<li>Strong organisational and communication skills, with attention to detail.</li>\n<li>Ability to work independently and collaboratively in a fast-paced environment.</li>\n<li>Willingness to travel as required (approximately 60%).</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>","enriched_at":1793009598270},{"id":"job_9ef7f431-298","title":"CRA II","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Malaysia-Kuala-Lumpur/Clinical-Research-Associate-II_JR160843","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>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.</p>\n<p><strong>Responsibilities</strong></p>\n<p>You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include:</p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li>\n<li>Performing data review and resolution of queries to maintain high-quality clinical data.</li>\n<li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<p>You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific or healthcare-related field.</li>\n<li>Minimum of 2 years of experience as a Clinical Research Associate.</li>\n<li>In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li>\n<li>Strong organisational and communication skills, with attention to detail.</li>\n<li>Ability to work independently and collaboratively in a fast-paced environment.</li>\n<li>Willingness to travel as required (approximately 60%).</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>","enriched_at":1793008963603},{"id":"job_ec98640b-521","title":"Start Up Lead","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Spain-Madrid/Clinical-Operations-Manager_JR161582","location":"Madrid","job_type":"full-time","experience_level":"senior","work_arrangement":"remote","category":"Healthcare","description":"<p>At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>As the world&#39;s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.</p>\n<p>This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, client policies and procedures, quality standards and adverse event reporting requirements internally and externally. The person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure Site Ready.</p>\n<p><strong>Key Responsibilities:</strong></p>\n<ul>\n<li>Ownership of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRAs).</li>\n<li>Oversees and tracks clinical research-related payments. Payment reconciliation at study close-out. Oversees FCPA, DPS/OFAC, and maintenance of financial systems. Financial forecasting in conjunction with SCOM /CRDs, other roles.</li>\n<li>Executes and oversees clinical trial country submissions and approvals for assigned protocols.</li>\n<li>Develops local language materials including local language Informed Consents and translations. Interacts with IRB/IEC and Regulatory Authority for assigned protocols.</li>\n<li>Manages country deliverables, timelines and results for assigned protocols to meet country commitments. Responsible for quality and compliance in assigned protocols in country.</li>\n<li>Contributes to the development of local SOPs.</li>\n<li>Coordinates and liaises with CTM, CTA, CRA, (Finance and Legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones.</li>\n<li>Collaborates closely with Headquarter to align country timelines for assigned protocols.</li>\n<li>Provides support and oversight to local vendors as applicable.</li>\n<li>Oversees and coordinates local processes, clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management. Enters and updates country information in clinical and finance systems.</li>\n<li>Ownership of local regulatory and financial compliance. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during study start-up.</li>\n<li>Required to in/directly influence investigators, external partners and country operations to adhere to budget targets and agreed payment timelines.</li>\n<li>Works in partnership internally with country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and sites, IRB/IECs and Regulatory Authorities in submission and approval related interactions. Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.</li>\n<li>Contribute or lead initiatives and projects adding value to the business.</li>\n<li>Contributes strongly to the team and other Country Operations roles knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required.</li>\n<li>Contributes to the team knowledge by acting as buddy/mentor and sharing best practices as appropriate/required.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>5-7 years of experience in clinical research or combined experience in Clinical Research and Finance/Business.</li>\n<li>Expertise of core clinical systems, tools and metrics.</li>\n<li>Excellent verbal and written influencing and training/mentoring skills, in local language and English.</li>\n<li>Strong coordination and organisational skills.</li>\n<li>Skilled knowledge of budget and contract negotiations, local regulatory environment and submission and approval processes, and understanding of how these impact study start-up.</li>\n<li>Ability to indirectly influence investigators, vendors, external partners and country managers to address and resolve issues, with minimal support from the manager.</li>\n<li>Ability to make decisions independently with limited oversight from the manager.</li>\n<li>Requires strong understanding of local regulatory environment.</li>\n<li>Ability to proactively develop risk management and mitigation plans in the country and resolve issues locally.</li>\n<li>Willingness to travel as required (approximately 25%).</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance related incentives.</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>","enriched_at":1793008856230},{"id":"job_26fcaa5a-8d4","title":"Clinical Research Associate","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Nevada/Clinical-Research-Associate_JR161778","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>As a Clinical Research Associate (CRA II) at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>You will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities:</strong></p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li>\n<li>Performing data review and resolution of queries to maintain high-quality clinical data.</li>\n<li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific or healthcare-related field.</li>\n<li>Minimum of 2 years of experience as a Clinical Research Associate.</li>\n<li>In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li>\n<li>Strong organisational and communication skills, with attention to detail.</li>\n<li>Ability to work independently and collaboratively in a fast-paced environment.</li>\n<li>Willingness to travel as required (approximately 60%).</li>\n</ul>\n<p><strong>Rewards &amp; Benefits:</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>","enriched_at":1793008091777},{"id":"job_2f84ef55-988","title":"Project Planner","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Spain-Madrid/Associate-Project-Manager_JR160900","location":null,"job_type":"full-time","experience_level":"mid","work_arrangement":null,"category":"Healthcare","description":"<p>At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>As the world&#39;s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.</p>\n<p>As an Associate Project Manager at ICON, you will support the coordination and management of clinical trials, contributing to the design, analysis, and advancement of innovative treatments and therapies.</p>\n<p><strong>What You Will Do:</strong></p>\n<p>You will oversee project and programme management workstreams, ensuring deliverables meet quality and timeline expectations. Key responsibilities include:</p>\n<ul>\n<li>Assisting project managers in the planning, execution, and monitoring of clinical trials.</li>\n<li>Coordinating study activities, including site selection, patient recruitment, and data collection.</li>\n<li>Supporting the development of study protocols, case report forms, and other study-related documents.</li>\n<li>Participating in data analysis and interpretation to support decision-making and regulatory submissions.</li>\n<li>Collaborating with cross-functional teams to ensure project milestones are met and deliverables are achieved.</li>\n</ul>\n<p><strong>Your Profile:</strong></p>\n<p>You will have solid project and programme management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline or healthcare-related field</li>\n<li>Minimum of 2 years of experience in clinical research or project management.</li>\n<li>Strong organisational and multitasking skills.</li>\n<li>Excellent communication and interpersonal skills.</li>\n<li>Ability to work effectively in a fast-paced and team-oriented environment.</li>\n<li>Willingness to travel as required (approximately 10%)</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>\n<p>Benefits may vary depending on role and location.</p>","enriched_at":1793007880623},{"id":"job_7b2ac0f5-c66","title":"Clinical Research Associate II","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/India-Bangalore/CRA-II_JR156746","location":"Mumbai","job_type":"full-time","experience_level":"senior","work_arrangement":"onsite","category":"Healthcare","description":"<p>At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.</p>\n<p><strong>Responsibilities</strong></p>\n<ul>\n<li>Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.</li>\n<li>Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.</li>\n<li>Collaborating with investigators and site staff to facilitate smooth study conduct.</li>\n<li>Performing data review and resolution of queries to maintain high-quality clinical data.</li>\n<li>Contributing to the preparation and review of study documentation, including protocols and clinical study reports.</li>\n</ul>\n<p><strong>Your Profile</strong></p>\n<ul>\n<li>Bachelor&#39;s degree in a scientific or healthcare-related field.</li>\n<li>Minimum of 3 years of experience as a Clinical Research Associate &amp; On-Site Monitoring.</li>\n<li>In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.</li>\n<li>Current or Prior experience in Therapeutic Areas like Oncology or Immunology or Cardiology or Gastroenterology or Pulmonology is a Must.</li>\n<li>Strong organisational and communication skills, with attention to detail.</li>\n<li>Ability to work independently and collaboratively in a fast-paced environment.</li>\n<li>Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver&#39;s license.</li>\n</ul>\n<p><strong>Rewards &amp; Benefits</strong></p>\n<ul>\n<li>Competitive base salary and performance-related incentives.</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable.</li>\n<li>Retirement and pension plans.</li>\n<li>Life assurance and disability coverage.</li>\n<li>Employee assistance programmes and wellbeing resources.</li>\n<li>Learning and development opportunities through structured training and career pathways.</li>\n</ul>","enriched_at":1793007850788},{"id":"job_3873e81b-21f","title":"Senior Clinical Research Associate, China","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Beijing/Clinical-Site-Manager-II_JR161930","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>As a Senior Clinical Research Associate at ICON Strategic Solutions, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p>You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:</p>\n<ul>\n<li>Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li>\n<li>Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</li>\n<li>Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</li>\n<li>Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</li>\n<li>Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</li>\n</ul>\n<p>You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline or healthcare-related field</li>\n<li>Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</li>\n<li>Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.</li>\n<li>Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</li>\n<li>Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</li>\n<li>Willingness to travel as required (approximately 60%).</li>\n</ul>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>","enriched_at":1793006372629},{"id":"job_4eea0329-85c","title":"Senior Clinical Research Associate, China","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/China-Beijing/Clinical-Site-Manager-II_JR161929-3","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>As a Senior Clinical Research Associate at ICON Strategic Solutions, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.</p>\n<p>You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include:</p>\n<ul>\n<li>Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.</li>\n<li>Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.</li>\n<li>Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.</li>\n<li>Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.</li>\n<li>Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.</li>\n</ul>\n<p>You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others. Required qualifications and experience:</p>\n<ul>\n<li>Bachelor&#39;s degree in a relevant scientific discipline or healthcare-related field</li>\n<li>Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.</li>\n<li>Proven ability to manage multiple sites and projects simultaneously, with strong organisational and problem-solving skills.</li>\n<li>Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.</li>\n<li>Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.</li>\n<li>Willingness to travel as required (approximately 60%)</li>\n</ul>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>\n<p>Benefits may include:</p>\n<ul>\n<li>Competitive base salary and performance-related incentives</li>\n<li>Health and wellbeing programmes including medical, dental, and vision coverage where applicable</li>\n<li>Retirement and pension plans</li>\n<li>Life assurance and disability coverage</li>\n<li>Employee assistance programmes and wellbeing resources</li>\n<li>Learning and development opportunities through structured training and career pathways</li>\n</ul>","enriched_at":1793006370106},{"id":"job_33df4f66-7ba","title":"Sr. Site Management Associate (French Speaking)","source_url":"https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Canada-Montreal/Sr-Site-Management-Assoociate_JR161646","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Healthcare","description":"<p>As a Sr. Site Management Associate (French Speaking) at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON&#39;s global expertise.</p>\n<p>You will serve as the primary point of contact for site administration and logistical needs during enrollment and maintenance and Data Base Lock (DBL).</p>\n<p>Key responsibilities include:</p>\n<ul>\n<li>Clinical Trial Execution &amp; Site Support:</li>\n<li>Collaborate with PIs and study coordinators to troubleshoot technical and administrative activities and issues</li>\n<li>Ensure timely site support and sustained engagement through consistent communication, proactive problem-solving, and appropriate follow-up</li>\n<li>Track and monitor documentation and systems information to ensure compliance and quality standards are maintained</li>\n<li>Regulatory &amp; Documentation Oversight:</li>\n<li>Support maintenance and update of the Trial Master File (TMF) with essential enrollment and maintenance documentation</li>\n<li>Ensure documentation of patient-related activities, deviation handling, and site correspondence aligns with GCP and internal SOPs</li>\n<li>Operational Efficiency &amp; Collaboration:</li>\n<li>Collaborate with monitors, CRLs, and cross-functional teams to identify unique and trending needs, operational risks, and site administrative feedback</li>\n<li>Utilize internal tracking tools and systems to ensure real-time visibility into site status/compliance</li>\n</ul>\n<p>Requirements:</p>\n<ul>\n<li>Bachelor&#39;s degree with at least 2 years of experience in clinical research</li>\n<li>Knowledge of Good Documentation Practices</li>\n<li>Systems experience (Veeva, TMF) highly preferred</li>\n<li>Understanding of the overall clinical development paradigm</li>\n<li>Must be bilingual: French/English</li>\n</ul>\n<p>ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.</p>","enriched_at":1793006367591}],"category_normalised":[{"category":"healthcare","count":46},{"category":"operations","count":2},{"category":"data science","count":2},{"category":"finance","count":1}],"velocity":{"weeks":[{"week_start":"2026-10-19","count":51}],"trend":"stable","wow_pct":0},"momentum":{"recent_14d":51,"prior_14d":0,"growth_pct":0,"classification":"stable"},"salary_vs_industry":{"company_median":124335,"industry_median":null,"percentile":null,"sample_size":5,"by_region":[{"region":"Unknown","company_median":124335,"industry_median":null,"sample":3},{"region":"United States","company_median":130554,"industry_median":null,"sample":2}],"transparency_pct":10,"industry_transparency_pct":0,"transparency_warning":true},"market_share":{"company_jobs":51,"industry_total":51,"share_pct":100,"rank":1,"peer_count":1},"ai_exposure":{"occupation_weighted_score":0.21,"skill_weighted_score":0.237,"top_exposed_titles":[{"title":"Clinical Research Associate II","count":3,"score":0.245},{"title":"Senior Clinical Research Associate, China","count":2,"score":0.245},{"title":"Clinical Research Associate","count":2,"score":0.245}],"top_exposed_skills":[{"skill":"Clinical Research","count":5,"score":0.255},{"skill":"Oncology","count":4,"score":0.245},{"skill":"Good Clinical Practice GCP","count":3,"score":0.245},{"skill":"Clinical Trial Monitoring","count":7,"score":0.245},{"skill":"Data Integrity","count":3,"score":0.245},{"skill":"Site Management","count":3,"score":0.245},{"skill":"Ich-gcp Guidelines","count":5,"score":0.245},{"skill":"Organisational Skills","count":3,"score":0.245},{"skill":"Data Analysis","count":5,"score":0.208},{"skill":"Ich-gcp","count":4,"score":0.199}]},"peer_set":[],"skills_lq":[],"geographic_shift":{"current":[{"region":"United States","count":4,"share_pct":33.3},{"region":"Latin America","count":2,"share_pct":16.7},{"region":"Unknown","count":2,"share_pct":16.7},{"region":"APAC","count":2,"share_pct":16.7},{"region":"India","count":1,"share_pct":8.3},{"region":"EU","count":1,"share_pct":8.3}],"emerging":[{"region":"United States","recent_30d":4,"prior_30d":0,"growth_pct":100}],"shrinking":[]},"seniority_anomalies":{"exec_recent_30d":1,"exec_prior_90d_avg":0,"exec_growth_pct":100,"notable_exec_hires":[{"title":"Medical Director/Medical Monitor","location":null,"posted_at":"2026-10-26"}]},"posting_dynamics":{"median_days_open":null,"industry_median_days_open":null,"long_open_count":0,"closure_rate_pct":0}}}}