Lead creative development and oversight of original scripted programming for STARZ, managing projects from development through production and post-production.
Compensation
Estimated Starting Range: $170,835-$278,670 per year (Note: The salary range listed above is specific to the locale for our Los Angeles, CA office.)
Responsibilities
Manage creative development and day-to-day oversight of assigned original scripted projects
Build and maintain relationships with writers, producers, directors, agents, managers, and studio partners
Source and evaluate pitches, scripts, intellectual property, and submissions
Guide creators and producers through development on assigned projects
Provide ongoing creative oversight during production and post-production
Requirements
Bachelor’s degree in Film/Television, Creative Writing, English, Communications, or a related field, or equivalent relevant experience
Nice to have: Bachelor’s degree in Film/Television, Creative Writing, English, Communications, or a related field
Drive growth across IQVIA Digital’s portfolio within large pharmaceutical accounts, focusing on Behavioral Insights, Advanced Practice Provider Strategy, and Email Marketing Solutions.
Locations (2)
Houston, Texas, United States
United States
Compensation
The potential base pay range for this role, when annualized, is $89,900.00 - $250,400.00. 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.
Responsibilities
Achieve growth and revenue targets for assigned IQVIA Digital solutions through consultative sales
Serve as subject matter expert for assigned solutions
Partner with account teams to develop account strategies and build pipeline
Build and maintain relationships with key client stakeholders
Identify opportunities within existing customers to expand relationships
This role leads regulatory initiatives for enterprise-wide products or platforms, drives regulatory strategy, and collaborates with executive and cross-functional teams for compliance and market expansion.
Responsibilities
Develop global regulatory strategies for complex product portfolios.
Advise executives and teams on regulatory risks, trends, and compliance options.
Lead complex regulatory strategy, regulatory submissions, agency communications for the US and Canada.
Lead response to major regulatory agency inquiries, inspections, and audits.
Develop training materials on new regulations and regulatory changes.
Lead the development and execution of the publication strategy and tactical plan for Oncology global clinical studies and related research outputs.
Compensation
The annual base pay for this position ranges from $193,000 to $289,900. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
Responsibilities
Lead the development and execution of the publication strategy and tactical plan for Oncology global clinical studies in humans from Phase Ib-IV, and non-clinical trial sources including health economics and outcomes research, epidemiology, real-world evidence (RWE), payer, and non-interventional studies.
Head the development of scientific, clinical and RWE planning data into timely publications for prescribers, payers, and patients through disease state and medicine insights.
Day-to-day management of assigned publication plans, delivery of outputs, financial tracking and meeting activities, working closely with all members of the delivery team and external alliances.
Lead external agency partners to ensure the accuracy of publication plan and publication results with respect to time, quality and cost, and ensuring accurate compliance documentation.
Solution Sales Specialist, Large Pharma, IQVIA Digital (Remote)Lifelancer · Remote, US+1 more
Director, Global Oncology PublicationsAstraZeneca · Gaithersburg, US