clinical lead

Opcare, part of the AM Healthcare, is the largest supplier of prosthetic and orthotic services to the NHS. As a company we aim to continuously improve the services we deliver and develop those who work for us. Job Summary We are currently seeking an experienced Prosthetist Clinical Lead who is looking for an opportunity to develop their career and be a part of our large and dynamic team in Cambridge. The role will involve working with a complex clinical case load and therefore clinical expertise in at least one area of prosthetics is essential, but there will also be opportunities to develop into different specialities. The role holder will be instrumental in managing the prosthetic clinical team and providing support and insight to the technical team and wider NHS MDT to advance and improve the delivery of the service. The role holder will be an integral member of the senior clinical team within Opcare and will provide mentoring support to less experienced prosthetists, graduates, and students. Main duties of the job Key Responsibilities<ul><li>Line management of the Prosthetics clinical team</li><li>Reporting responsibilities with regards to delivery of the service in line with NHS and internal key performance indicators</li><li>Ensure the delivery of high-quality care for all patients and the smooth running of the service</li><li>Work closely with multi-disciplinary teams (MDTs) across Cambridgeshire and the wider Trust including Surgeons and Consultants</li><li>Share your knowledge and experience with junior colleagues and offer mentorship to graduates and students</li><li>Help coordinate and contribute to in-service training sessions</li><li>The role holder will be a registered Prosthetist able to support development and service improvements for the betterment of patients in the county of Cambridgeshire</li><li>The successful candidate will join an enthusiastic and busy team, and be supported with local, regional, and national training to develop their clinical and managerial skills to support the service</li></ul>We aim to deliver a first-class service for users whilst applying the most advanced and exciting clinical and technical solutions available to patients. About us Working at Cambridge Opcare has been providing the Prosthetic and Orthotic Service in Cambridgeshire since 2009. This role is an excellent opportunity to have a key influence within the service to advance and improve the delivery of the service. The Prosthetic Department is based in our brand-new facility in Great Shelford, Cambridge. This is a purpose-built facility for the delivery of our services, where we provide outpatient and community prosthetic care for a wide variety of patients. There is a complex mix of Adult and Paediatric MDTs and extended practice clinics which provide a great opportunity to be exposed to interesting and varied caseloads.Onsite at Cambridge, we work closely with the gait lab team, specialist physiotherapists and orthopaedic surgeons for surgical and medical planning pathways for paediatric and adult amputees. There is opportunity to work across company networks and groups including 3D manufacturing, scanning and clinical governance projects. What do we offer? Competitive market salaryIndustry leading training opportunitiesAccess to innovative scanning and 3D technologyManagement developmentAccess to UK & Global clinical conferencesTo apply please email your CV with a cover letter ASAP to Job responsibilities Job title Clinical Lead ProsthetistLocation Great Shelford, CambridgeOpcare, part of the AM Healthcare, is the largest supplier of prosthetic and orthotic services to the NHS. As a company we aim to continuously improve the services we deliver and develop those who work for us.Looking to take the next step upwards in your career pathway?Looking to join one of the fastest growing clinical service delivery companies in the UK?Do you want to join an organisation and team that believes in putting the patient first and focuses on improving the lives of individuals through innovation and service development?Want to join a team that focuses on staff and people development?Working at CambridgeOpcare has been providing the Prosthetic and Orthotic Service in Cambridgeshire since 2009. This role is an excellent opportunity to have a key influence within the service to advance and improve the delivery of the service. The Prosthetic Department is based in our brand new facility in Great Shelford, Cambridge. This is a purpose-built facility for the delivery of our services, where we provide outpatient and community prosthetic care for a wide variety of patients. There is a complex mix of Adult and Paediatric MDTs and extended practice clinics which provide a great opportunity to be exposed to interesting and varied caseloads.Onsite at Cambridge, we work closely with the gait lab team, specialist physiotherapists and orthopaedic surgeons for surgical and medical planning pathways for paediatric and adult amputees. Alongside the specialist clinics, the role leads and supports the day-to-day delivery of prosthetic services within the county. There is opportunity to work across company networks and groups including 3D manufacturing, scanning and clinical governance projects.Job Summary:We are currently seeking an experienced Prosthetist Clinical Lead who is looking for an opportunity to develop their career and be a part of our large and dynamic team in Cambridge. The role will involve working with a complex clinical case load and therefore clinical expertise in at least one area of prosthetics is essential, but there will also be opportunities to develop into different specialities. The role holder will be instrumental in managing the prosthetic clinical team and providing support and insight to the technical team and wider NHS MDT to advance and improve the delivery of the service. The role holder will be an integral member of the senior clinical team within Opcare and will provide mentoring support to less experienced prosthetists, graduates, and students.Key ResponsibilitiesSome of the key responsibilities the role holder will have<ul><li>Line management of the Prosthetics clinical team</li><li>Reporting responsibilities with regards to delivery of the service in line with NHS and internal key performance indicators</li><li>Ensure the delivery of high quality care for all patients and the smooth running of the service</li><li>Work closely with multi-disciplinary teams (MDTs) across Cambridgeshire and the wider Trust including Surgeons and Consultants</li><li>Share your knowledge and experience with junior colleagues and offer mentorship to graduates and students</li><li>Help coordinate and contribute to in-service training sessions</li><li>The role holder will be a registered Prosthetist that can support development and service improvements for the betterment of patients in the county of Cambridgeshire</li><li>The successful candidate will join an enthusiastic and busy team, and be supported with local, regional, and national training to develop their clinical and managerial skills to support the service</li></ul>Qualifications<ul><li>BSc Prosthetics and Orthotics</li><li>Certified Prosthetist</li><li>HND Prosthetics</li><li>Must also be fully HCPC Registered</li></ul>What do we offer?Competitive market salaryIndustry leading training opportunitiesAccess to innovative scanning and 3D technologyManagement developmentAccess to UK & Global clinical conferencesAbility Matters Group Limited are an equal opportunities employer, we have a clear goal of driving diversity and inclusion across all operations of the group. Person Specification Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

Clinical Lead Prosthetist

Greys Specialist Recruitment

Exciting Opportunity: Occupational Health Manager Clinical LeadAre you a passionate and experienced Registered Nurse looking to take the next step in your occupational health career?We have an excellent opportunity for a dedicated Occupational Health Manager to join a successful organisation in beautiful Barrow in Furness!Position: Occupational Health Manager Clinical LeadLocation: Barrow in Furness Type: Full-Time, PermanentHours: Monday to Friday, 8am - 4pm (On-site)What You'll Be Doing:You will play a pivotal role in guiding and supporting our clinical team, ensuring the delivery of high-quality occupational health services. Your responsibilities will include conducting clinical competency reviews, leading wellbeing initiatives, and helping to coordinate programs that promote employee health and safety.What We're Looking For:<ul><li>A registered nurse with a valid NMC pin</li><li>Proven experience working as an Occupational Health Advisor</li><li>Strong leadership skills with the ability to support and motivate a clinical team</li><li>A proactive approach to wellbeing and health promotion</li></ul>Apply today and take the next step in your occupational health career!

Occupational Health Manager Clinical Lead

Southern NSW Local Health District

CCLHD - Clinical Lead - Mental Health - Whole Family Team Employment Type:Permanent Full Time Position Classification:Health Clinician Level 4 Remuneration:Dependent Upon Qualifications Hours Per Week:38 Location:Central Coast Requisition ID:REQ617656 Applications Close:Sunday, 9 November 2025 at 11.59pm At Central Coast Local Health District (CCLHD), we are committed to Trusted Care, Better Health for Everyone. We are seeking a passionate and motivated Clinical Lead - Mental Health to join the Whole Family Team (WFT), part of CCLHD's integrated Violence, Abuse and Neglect (VAN) Service. About the Opportunity As the Clinical Lead - Mental Health, you will work alongside the Clinical Lead - Drug and Alcohol to provide clinical leadership, supervision, and education to a multidisciplinary team of dedicated clinicians. The Whole Family Team provides intensive, family-focused therapeutic support to vulnerable families across the Central Coast, where parental mental health and/or substance use places children at risk of significant harm (ROSH). Working in close partnership with the Department of Communities and Justice (DCJ), WFT delivers trauma-informed interventions - most often in the home - to help parents strengthen their parenting capacity and family functioning so children can safely remain with their families. Thisrole is suitable for the following - Clinical Nurse Consultant Grade 2, Occupational Therapist Level 4, Senior Psychologist, Social Worker Level 4. In this role you will: <ul> <li>Provide expert clinical leadership, supervision, and mentoring to the Whole Family Team.</li> <li>Support the development and delivery of evidence based, trauma informed, and culturally safe interventions for families.</li> <li>Manage a clinical caseload and provide specialist mental health assessment, formulation, and treatment planning.</li> <li>Communicate effectively with patients, families, and the healthcare team to promote a supportive environment.</li> <li>Lead quality improvement initiatives, professional development, and clinical research activities.</li> <li>Contribute to service innovation that aligns with the NSW Health PARVAN Framework, policies, and best practice standards.</li> <li>A tertiary qualification and full registration with AHPRA as an Occupational Therapist, Nurse, or Psychologist, or eligibility for AASW membership as a Social Worker.</li> <li>Strong expertise in mental health assessment and intervention, with experience supporting families where parental mental health and/or substance use affects child wellbeing.</li> <li>Proven leadership and clinical supervision skills, with the ability to guide, mentor, and support a multidisciplinary team.</li> <li>Excellent collaboration and communication skills, with experience building effective partnerships across health, community, and government sectors.</li> <li>Committed to teamwork within a multidisciplinary environment.</li> <li>A commitment to continuous improvement, demonstrated through leading quality initiatives and maintaining up to date knowledge in leadership and mental health practice.</li> </ul> Applicants must have current work rights in Australia or be a permanent resident or citizen. Unfortunately, we cannot consider applicants who do not meet this requirement. <ul> <li>Work Life Balance: Enjoy an accrued day off each month, 17.5% annual leave loading, and paid parental leave.</li> <li>Financial Benefits: Boost your take home pay with salary packaging, save on car costs with novated leasing, and access relocation assistance.</li> <li>Health & Wellbeing: Stay active with discounted gym memberships (Fitness Passport), free flu vaccinations, telehealth support, and confidential Employee Assistance Program (EAP) counselling for you and your family. Plus, access discounted private health insurance.</li> <li>Career Growth: Advance your career with free professional development courses and secondment opportunities.</li> </ul> Working for Central Coast Local Health District - NSW Health Central Coast Local Health District is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Aboriginal and Torres Strait Islander applicants can access support through the Stepping Up initiative, which provides guidance on the NSW Health recruitment process. You are also welcome to reach out to Nathan Bramston in our Aboriginal Workforce Development Team at or call for one on one support. All NSW Health workers are required to comply with the Occupational Assessment, Screening and Vaccination Against Specified Infectious Diseases Policy Directive. This includes: <ul> <li>Category A positions: Mandatory evidence of protection against specified infectious diseases, including annual influenza vaccination and tuberculosis assessment.</li> <li>Category B positions: Vaccination is recommended but not mandatory.</li> </ul> NSW Health strongly recommends all workers stay up to date with COVID 19 vaccinations as per the Australian Technical Advisory Group on Immunisation guidelines. However, COVID 19 vaccination is not a condition of employment. Additional Information An Eligibility List (E List) or talent pool may be created from this recruitment episode to assist in filling future permanent, temporary, or casual full time and part time positions. You are encouraged to complete applications on a weekday where Technical Support is available Monday to Friday 8.30am to 4.30pm by phoning ROB Help Desk on . NSW Health acknowledges the people of the many traditional countries and language groups of New South Wales. It acknowledges the wisdom of Elders past and present, and pays respect to all Aboriginal communities of today.

CCLHD - Clinical Lead - Mental Health - Whole Family Team

Ray-CRO

Calling Clinical Project Leaders &ndash; EgyptAt RAY-CRO, we don&rsquo;t just execute studies &mdash; we lead them, own them, and deliver real impact.As we expand our regional clinical operations, we are looking for an experienced Clinical Project Leader (CPL) who can:Take full ownership of clinical studies from start to finish Serve as the primary point of contact for sponsors and key stakeholders Lead CRAs and cross-functional teams with confidence and clarity Drive timelines, quality, and compliance across Egypt &amp; KSA Proactively manage risks, decisions, and escalations with accountabilityIf you are someone who: Thinks beyond tasks and focuses on outcomes Thrives in sponsor-facing roles and high-responsibility environments Brings solid CRO or pharma clinical project experienceThis role is made for you.Location: Egypt Apply: careers@ray-cro.comJob Type: Full-time

Clinical Project Lead

Roche

<div>Bei Roche kannst du ganz du selbst sein und wirst f&uuml;r deine einzigartigen Qualit&auml;ten gesch&auml;tzt. Unsere Kultur f&ouml;rdert pers&ouml;nlichen Ausdruck, offenen Dialog und echte Verbindungen. Hier wirst du f&uuml;r das, was du bist, wertgesch&auml;tzt, akzeptiert und respektiert. Dies schafft ein Umfeld, in dem du sowohl pers&ouml;nlich als auch beruflich wachsen kannst. Gemeinsam wollen wir Krankheiten vorbeugen, stoppen und heilen und sicherstellen, dass jeder Zugang zur Gesundheitsversorgung hat &ndash; heute und in Zukunft. Werde Teil von Roche, wo jede Stimme z&auml;hlt.<div></div><div>
Die Position</div>
The role focuses on the responsibilities to ensure leadership and execution of one or more sponsored interventional trials or managed primary data collection non-interventional studies, the effective and efficient delivery of all operational aspects in accordance with the appropriate quality standards including ICH/GCP and GVPs/GPPs.
Your Responsibilities<ul><li>
Ensures study adherence to appropriate guidelines (ICH GCP/GVP/GPP), relevant regulations and Roche procedural documents. Ensures study inspection readiness at all times. Ensures the completion and finalization of any corrective and preventive action plans resulting from site audits and inspections</li><li>
Provides operational input and insights into the development of study protocols, Clinical Study Reports, informed consent form and protocol feasibility questionnaires</li><li>
Promotes operational excellence. Oversees the delivery and maintenance of essential study plans and systems (e.g. site &amp; country selection and monitoring plan; study tracking systems, clinical supply; vendor oversight plan; RBQM or equivalent risk management activities). Ensures accurate tracking and reporting of study metrics</li><li>
Chairs Study Management Team meetings and organizes the investigator meetings and study kick-off meetings</li><li>
Establishes and maintains study budgets and approves invoices, identifies and communicates any issues/variances with study budgets and action plans for resolution</li><li>
Accountable for all vendor related operational study deliverables, according to timelines, budget, operational procedures, quality/compliance and performance standards. Leads vendor selections by reviewing proposals and providing recommendations, reviews and negotiates clinical work orders. Maintains oversight of vendor performance, issues, and their resolution and identifies systematic issues and coordinates any corrective action. Ensures vendors receive appropriate training.</li><li>
Ensures proper handling of all study close out activities including but not limited to the site close out, final drug accountability, final safety reconciliation and Inspection readiness of Trial Master File documentation.</li></ul>
Who you are<ul><li>
Strong leadership skills developed through leading successful multi-functional matrix study teams through all stages of clinical studies.</li><li>
Proven strategic capabilities, organizational awareness and proactive planning with embedded contingencies and risk management mindset.</li><li>
Clear understanding and experience applying ICH/GCP and/or GVP/GPPs and applicable regulations including awareness of quality requirements.</li><li>
Well-developed written and verbal communication skills demonstrated by an ability to present clear instructions/directions, to motivate your team, negotiate with peers and partners and influence cross functionally.</li><li>
Excellent problem solving, negotiation and conflict resolution skills</li><li>
Borderless Collaboration: working closely with other countries/communities/teams, embracing the loop of &lsquo;sharing and learning together&rsquo; to co-create Solutions</li><li>
Budget Management- cost effective management with limited unforeseen cost overruns.</li></ul><div> 
Wer wir sind</div>
Eine ges&uuml;ndere Zukunft treibt uns zur Innovation an. Mehr als 100.000 Mitarbeiter weltweit arbeiten gemeinsam daran, wissenschaftliche Fortschritte zu erzielen und sicherzustellen, dass jeder Zugang zur Gesundheitsversorgung hat &ndash; heute und f&uuml;r zuk&uuml;nftige Generationen. Durch unser Engagement werden &uuml;ber 26 Millionen Menschen mit unseren Medikamenten behandelt und mehr als 30 Milliarden Tests mit unseren Diagnostik-Produkten durchgef&uuml;hrt. Wir ermutigen uns gegenseitig, neue M&ouml;glichkeiten zu erkunden, Kreativit&auml;t zu f&ouml;rdern und hohe Ziele zu setzen, um lebensver&auml;ndernde Gesundheitsl&ouml;sungen zu liefern.
Gemeinsam k&ouml;nnen wir eine ges&uuml;ndere Zukunft gestalten.
Roche ist ein Arbeitgeber, der die Chancengleichheit f&ouml;rdert.</div>

Clinical Study Lead

IQVIA

<div><div><div>Malvern, United States of America | Full time | Home-based | R1520965</div><div><div>
Job available in additional locations</div></div></div><div><div> 
IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.</div><div>
Job Overview 
Associate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients&rsquo; lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Associate Clinical Leads partner with Project Leaders and other functional teams to secure delivery requirements are met at all times. 
 
Essential Functions 
<ul><li>Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).</li><li>Accountable for meeting projects&rsquo; recruitment targets and ensuring appropriate recruitment strategies are in place.</li><li>Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project&rsquo;s lifecycle.</li><li>Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.</li><li>Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.</li><li>Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.</li><li>Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.</li><li>Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.</li><li>Conduct regular team meetings and communicate appropriately to achieve objectives.</li><li>Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.</li><li>May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;</li><li>May attend site visits as applicable in support of project delivery.</li></ul> 
Qualifications 
<ul><li>Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required</li><li>Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience.;</li><li>Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;</li><li>Requires broad protocol knowledge and therapeutic knowledge.;</li><li>Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.</li><li>Requires basic understanding of project finances.;</li><li>Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;</li><li>Communication - Strong written and verbal communication skills including good command of English language.</li><li>Problem solving - Problem solving skills.</li><li>Organization - Planning, time management and prioritization skills.</li><li>Prioritization - Ability to handle conflicting priorities.</li><li>Quality - Attention to detail and accuracy in work.</li><li>Results-oriented approach to work delivery and output.; and PowerPoint.;</li><li>IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.;</li><li>Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li><li>Cross-collaboration - Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.</li><li>Effective communication - Ability to influence without authority.</li><li>IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).</li></ul></div><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div><div>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</div>
The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

Clinical Trial Manager I, IQVIA Biotech

<div><div><div>Springfield, United States of America | Full time | Home-based | R1520965</div><div><div>
Job available in additional locations</div></div></div><div><div> 
IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.</div><div>
Job Overview 
Associate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients&rsquo; lives by bringing new drugs to the market faster. The Associate Clinical Lead is a member of the core project team responsible for clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Associate Clinical Leads partner with Project Leaders and other functional teams to secure delivery requirements are met at all times. 
 
Essential Functions 
<ul><li>Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).</li><li>Accountable for meeting projects&rsquo; recruitment targets and ensuring appropriate recruitment strategies are in place.</li><li>Contribute to the development of the project risk mitigation plan and manage clinical risks throughout the project&rsquo;s lifecycle.</li><li>Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.</li><li>Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.</li><li>Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.</li><li>Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.</li><li>Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.</li><li>Conduct regular team meetings and communicate appropriately to achieve objectives.</li><li>Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.</li><li>May work as the sole Clinical Lead on projects with 1-2 service lines and single/few countries or alongside more senior Clinical Leads to deliver large, global trials.;</li><li>May attend site visits as applicable in support of project delivery.</li></ul> 
Qualifications 
<ul><li>Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required</li><li>Requires 3 years clinical research/monitoring experience or equivalent combination of education, training and experience.;</li><li>Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.;</li><li>Requires broad protocol knowledge and therapeutic knowledge.;</li><li>Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.</li><li>Requires basic understanding of project finances.;</li><li>Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e., International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.;</li><li>Communication - Strong written and verbal communication skills including good command of English language.</li><li>Problem solving - Problem solving skills.</li><li>Organization - Planning, time management and prioritization skills.</li><li>Prioritization - Ability to handle conflicting priorities.</li><li>Quality - Attention to detail and accuracy in work.</li><li>Results-oriented approach to work delivery and output.; and PowerPoint.;</li><li>IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.;</li><li>Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.</li><li>Cross-collaboration - Ability to work across cultures and geographies with a high awareness and understanding of cultural differences.</li><li>Effective communication - Ability to influence without authority.</li><li>IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).</li></ul></div><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div><div>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</div>
The potential base pay range for this role, when annualized, is $68,400.00 - $171,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div></div><div></div>

Search 10000+ Clinical lead jobs near you this January. New roles added regularly across leading industries. Apply today.

10000 clinical lead jobs NEAR_ME

Clinical Lead Prosthetist

Occupational Health Manager Clinical Lead

CCLHD - Clinical Lead - Mental Health - Whole Family Team

Clinical Project Lead

Clinical Study Lead

Clinical Trial Manager I, IQVIA Biotech

Clinical Trial Manager I, IQVIA Biotech