Clinical Project Manager Jobs

Clinical Project Manager, IQVIA Biotech Immuno-Oncology and Cell and Gene Therapy

Clinical Project Manager

Clinical Project Manager

Established in 1996 and rebranded to Scout in 2024, we built our foundation on planning meetings for numerous organizations within the life sciences sector (Scout Meetings). In response to emerging industry needs, we expanded our services to include Scout Clinical, one of the top providers of clinical trial patient travel and reimbursements, and Scout Academy, our secure, online, on-demand learning management system that ensures global compliance. Scout is recognized as a leader in our field for innovation in service, attention to detail, our stellar team members, and making the complex easier. If this interests you, we’d love to have you join our rapidly growing team! Position Summary: We are looking to hire a talented and eager Clinical Project Manager to join our UK team in a remote position. The Project Manager will perform a wide variety of activities to support the start-up, management, and completion of patient services for clinical research studies. Responsibilities of this position include, but are not limited to: Contracts support Review protocols in support of new requests for proposal or assigned projects Study management activities and study start-up Maintain required study tracking database to accurately reflect the status of the studies and deliverables Regular communication with global study stakeholders including CRO and Sponsors. Managing client expectations and escalations. Schedule and lead study, Kick of Meetings, Investigators’ Meetings, and follow-up calls Act as main point of contact to Sponsor and CRO clients for Scout Clinical services for assigned studies Collaborate on operational internal policies and manage adherence Oversee regulatory onboarding process of studies in collaboration with Scout Clinical Compliance Team Manage preparation of study-specific patient and site-facing documentation throughout the life of the study Manage training of sites, and study teams on utilization of the Scout portal as needed Oversee and manage Scout Clinical portal configuration for assigned studies Work with Patient Liaison team to support travel and reimbursement activities associated with assigned studies Review and manage study utilization and financial metrics. The ideal candidate will have the following experience, skills, and knowledge: Bachelor’s Degree or equivalent experience Experience in the clinical/healthcare industry, preferably clinical research Strong understanding of project management Strong understanding of the clinical trial process and clinical trial protocols Ability to handle multiple projects in various planning stages concurrently Ability to track and manage key dates/deadlines The ideal candidate will have the following competencies and qualities: The desire to learn/be coachable Timely, professional, courteous communication with clients, vendors and colleagues Attention to detail Well organized with an ability to prioritize and multi-task Ability to work within and meet strict deadlines Ability to work under pressure in a fast paced, demanding environment Forward thinking / problem solver / critical thinker / analytical Team player Visit our website at www.scoutclinical.com or follow us on LinkedIn for other employment opportunities. WE ARE AN EQUAL OPPORTUNITY EMPLOYER VnUgztzkvo

Clinical Project Manager

Clinical Project Manager, IQVIA Biotech

Bloemfontein, South Africa | Full time | Home-based | R1522869Job available in additional locations 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.Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices.Clinical Project Management, IQVIA Biotech is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA’s suite of solutions to drive operational excellence and strategic leadership with our customers.Main Responsibilities Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures. Set objectives of the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance. Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies. May be responsible for delivery and management of smaller, less complex, regional studies. Develop integrated study management plans with the core project team. Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles. Monitor progress against contract and prepare project information proactively to stakeholders internally and externally. Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts. Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and implementing appropriate corrective and preventative action plans. May serve as primary or backup project contact with customer and would then own the relationship with the project’s key customer contacts, as well as collaborate with IQVIA business development representatives. Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles. Ensure the financial success of the project. Forecast and identify opportunities to accelerate activities to bring revenue forward. Identify changes in scope and manage change control process as necessary. Provide input to line managers of their project team members’ performance relative to project tasks. Support staff development and mentor less experienced project team members on assigned projects to support their professional development. Required Skills and Qualifications Bachelor's Degree Life sciences or related field. 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience. Advanced knowledge of job area, typically obtained through advanced education combined with experience. Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge; therapeutic area knowledge in any of the following would be an advantage: cardiovascular - metabolic, renal, obesity. Good understanding of project financials including experience managing, contractual obligations and implications. Good understanding of the competitive environment and how to communicate value through IQVIA Biotech solutions. Strong written and verbal communication skills including very good command of English language. Strong customer service skills and presentation abilities. Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently. Ability to make decisions, bringing clarity to disparate information to inform actions and drive results. Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances. Results-oriented approach to work towards delivery and output. Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving. Good software and computer skills. Ability to work across geographies displaying high awareness and understanding of cultural differences. May require occasional travel to the United States. 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

Clinical Project Manager

Project Manager (Clinical Systems)

Senior Project Manager (Clinical Trials)

Senior Project Manager (Clinical Trials)

Senior Project Manager (Clinical Trials)

Senior Project Manager (Clinical Trials)

Manager – Clinical Projects (SEHA HQ)

The Clinical Projects Manager (Physician) is responsible for leading and coordinating clinical initiatives, programs, and performance improvement projects that contribute to SEHA’s strategic and clinical excellence objectives. This position ensures integration of evidence-based practices, standardization of care, and delivery of high-quality outcomes across SEHA hospitals and clinics. Also bridges clinical leadership with operational and quality excellence across all SEHA health care facilities and aligns with Department of Health (DOH) standards.

Senior Clinical Project Manager

$170,000 - $190,000/yr

The Opportunity Our Client, a rapidly growing biotech company at the forefront of cutting edge research is searching for a Senior Clinical Project Manager to take the reins of their global clinical programs. This is a newly created and highly influential role, designed to support a fast-moving pipeline as the organisation heads toward a pivotal Phase III study launching in 2026. This position, reporting to the VP of Clinical, comes at a critical and exciting time with significant milestones and…

Senior Clinical Project Manager

$170,000 - $190,000/yr

The Opportunity Our Client, a rapidly growing biotech company at the forefront of cutting edge research is searching for a Senior Clinical Project Manager to take the reins of their global clinical programs. This is a newly created and highly influential role, designed to support a fast-moving pipeline as the organisation heads toward a pivotal Phase III study launching in 2026. This position, reporting to the VP of Clinical, comes at a critical and exciting time with significant milestones and…