The successful candidate will accelerate disease state awareness by providing education programs for professional staff, including doctors, nurses, and other key healthcare staff through 1:1 presentations, round table discussions, and formal presentations.

Key responsibilities include:

• Accepting all assignments within 24 hours of receiving notification
• Notifying the manager if unable to accept a patient assignment or schedule a patient visit within 72 hours due to other special circumstances
• Reporting any Adverse Event per guidelines
• Completing all reports and written assignments in a timely, accurate, and thorough manner
• Maintaining a high level of professional standards in all interactions with patients and customer contacts
• Reading, understanding, and adhering to important documents such as fraud and abuse guidelines, FDA guidelines, Pharma code, and HIPPA guidelines

The ideal candidate will have:

• A Bachelor's Degree or High School Diploma or equivalent
• Pharmaceutical industry experience preferred
• Clinical competence in the disease area
• Understanding and general knowledge of health services
• Good working knowledge of national clinical systems
• Ability to manage own workload with minimal guidance
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Current nursing or dietitian license in good standing
• Driver's License - Valid and In-State

IQVIA is committed to integrity in our hiring process and maintains a zero-tolerance policy for candidate fraud.

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Key responsibilities include:

• Supporting the design, development, and delivery of consulting projects or components of larger, complex projects
• Conducting market research to understand business needs and identify gaps and opportunities for clients
• Managing internal and external cross-functional stakeholders to support project delivery
• Leveraging internal and external subject matter expertise to identify potential solutions to client issues
• Working in a team to create reports, presentations, and workshops under the guidance of practice leaders
• Supporting the development of a broad knowledge of related consulting methodologies and pharmaceutical market thought leadership
• Working independently and as part of a high-performing team
• Attending, supporting, and presenting with confidence at client meetings

To be successful in this role, you will need:

• A Bachelor's or Master's degree in life sciences or economics/business, with a keen interest in life sciences or healthcare consulting
• Relevant internship or working experience is preferable
• Experience in consulting, pharmaceutical, or healthcare industry will be highly advantageous
• Demonstrable analytical and problem-solving skills
• Excellent verbal and written communication skills
• Good interpersonal skills, with an ability to work effectively with others
• Knowledge of key issues and current developments in the pharmaceutical and healthcare industries
• Knowledge of consulting methodologies, tools, and techniques
• Highly adaptable, with an ability to learn quickly and apply new knowledge
• A willingness and ability to travel for work

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Responsibilities

• Lead real-world evidence (RWE) study strategy development
• Partner with Sales, Medical, and Operations teams to develop competitive and operationally feasible solutions for client opportunities
• Provide expertise in protocol assessment, feasibility strategy, site and country selection, patient recruitment, and study execution planning
• Support proposal development, bid defense meetings, and client presentations
• Ensure effective transition of study strategy to project delivery teams and provide strategic guidance throughout study execution

Qualifications

• Bachelor's degree or above in Life Sciences, Pharmacy, Medicine, Public Health, or a related field
• 5+ years of experience in clinical research, clinical operations, real-world evidence (RWE), feasibility, or drug development
• Experience in at least one of the following areas: Clinical Project Management/Real World Evidence/ Feasibility / Protocol Development /Study Strategy

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Your responsibilities will include:

• Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
• Collaborating and communicating with a variety of colleagues and customers, with good knowledge of applicable clinical research regulatory requirements.

Qualifications:

• University degree in scientific discipline or healthcare
• At least 1 year of on-site monitoring experience
• Good knowledge of GCP and clinical research regulatory requirements
• Good computer skills including MS Office
• Excellent command of English language
• Organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with colleagues, managers, and customers
• Flexibility to travel

What you can expect:

• Working with different customers on global trials
• Career development opportunities for those who are passionate in wanting to grow as part of the organization
• Leaders that support flexible work schedules/arrangement
• Excellent working environment in a stable, international, reputable company
• Programs to help you build your technical skills, therapeutic knowledge and regular refreshers for updates in the regulatory landscape
• Attractive remuneration package

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Key responsibilities include:

• Reviewing Requests For Proposal (RFP) and identifying information for proposal text and budget development
• Working closely with the proposal development team to prepare and finalize proposals
• Preparing text and budget for proposals, rebids, and related documents
• Providing support and assistance to other Proposal Developers in the delivery of assigned opportunities
• Leading assigned projects to develop proposals and budgets
• Revising or developing preliminary agreements and related budgets and scope of work
• Ensuring the scope of work is defined correctly and budgets reflect the scope
• Participating in strategy calls to discuss customer requirements and identify discrepancies in customer information
• Performing quality control edits on all documents and participating in the finalization of documents and distribution to the customer and internal departments
• Updating and maintaining corporate databases as required and ensuring accurate information is included in tracking reports
• May participate in training/coaching/mentoring new staff
• May participate in customer meetings
• Participates in department initiatives
• Performing all other duties as assigned

Requirements:

• Bachelor's Degree in Life Science, Business Management or related field
• Minimum of 5 years direct experience in Contracts, Proposals, industry specific operations experience or equivalent combination of education, training and experience
• Knowledge of CRO Industry
• Knowledge of Microsoft Excel, Word, and understanding of costing models
• Ability to interpret RFPs and protocols
• Strong analytical skills and excellent verbal and written communication skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and customers

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Work with study(ies)/program(s) teams to focus on leveraging deep therapeutic expertise and IQVIA solutions to drive operational excellence and strategic leadership with our customers.

Essential Functions

• Participate in bid defense preparations and lead bid defense presentations in partnership with Business Development for large sized, multiple and full service, multiple country and/or multi regional studies.
• Develop and/or support on the preparation of integrated study management plans in collaboration with the core project team.
• Accountable for the strategic development and execution or delivery of clinical studies in line with agreed upon contracts while optimizing speed, quality and cost of delivery.
• Serve as primary project oversight and/or contact with customers and own relationship with the project’s key customer contact(s).
• Set objectives for the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance, providing feedback and leadership.
• 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/present project information proactively to all stakeholders internally and externally.
• Coach and/or mentor junior team members around project delivery, planning, project review, risk management and problem solving.
• Achieve project quality by identifying and proactively managing quality risks and issues.
• May participate in executive committees as part of program leadership.
• Ensure the financial success of the project including optimal management and assignment of resources to achieve project goals and profitability.

Qualifications

• Bachelor's Degree Life sciences or related field
• Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.
• Requires 10 years clinical research experience including 6 years of project management experience or equivalent combination of education, training and experience.
• Knowledge of clinical trials, ICH GCP and relevant local laws, regulations and guidelines.
• Strong written and verbal communication skills including good command of English language.
• Strong problem solving skills, negotiation and customer management skills.
• Ability to work through others to deliver results to the appropriate quality and timeline metrics.

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