Program Manager, Clinical Data Science, Sponsor Dedicated Job at iconplc

Executive Director, Global Clinical Operations

We are seeking an Executive Director, Global Clinical Operations, (GCO), who wil...

Location

United States

Salary:

285000.00 - 320000.00 USD / Year

Apogee Therapeutics

Expiration Date

Until further notice

Requirements

BA/BS in life sciences or equivalent
Minimum 20 years of clinical research experience, including at least 5 years leading global projects from inception to completion
Minimum of 7 years line management experience
Minimum of 3 years’ experience in Biotech industry strongly preferred
Significant knowledge of pharmaceutical industry, drug development and regulatory processes
Experience developing all clinical trial plans, including site management, risk assessment and mitigation strategies, recruitment and retention plans, etc.
Leader with growth mindset, willing to learn from others, committed to mentoring others and dedicated to promoting psychological safety
Ability to build and lead high-functioning teams, both within clinical operations and cross-functionally
Excellent communication skills with ability to develop strong relationships and present to a variety of stakeholders and tailor message accordingly
Strong project management skills with high sense of urgency, ability to collaborate and influence effectively cross-functionally

Job Responsibility

Manage and plan CTO resourcing for assigned programs
Lead, build and mentor CTO team supporting assigned program(s)
Serve as a member on Clinical Operations Leadership Team (COLT)
Create and support implementation of Clinical Operations processes, platforms and/or systems
Clinical operations representative on global development teams (GDT) and/or oversees direct reports serving on GDTs
Clinical operations representative on Program Teams (PT)
Lead problem solving and facilitate teams to identify clinical operations issues and propose solutions
Identify critical path items and evaluate variances to propose and oversee the implementation of proactive contingency plans
Compile, assess, and communicate risks and optionality to support informed decision making for operational strategy
Strong collaboration and partnership with cross functional colleagues globally

What we offer

Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
Three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
Commitment to growing you professionally and providing access to resources to further your development
Apogee offers regular all team, in-person meetings to build relationships and problem solve

Fulltime

Associate Director, Clinical Operations

We are seeking an Associate Director, Clinical Operations who will be accountabl...

Location

United States

Salary:

180000.00 - 195000.00 USD / Year

Apogee Therapeutics

Expiration Date

Until further notice

Requirements

BA/BS in life sciences or equivalent
8+ years of clinical research experience, including at least 3 years leading global projects from inception to completion
2+ years’ experience in Biotech industry strongly preferred
Significant knowledge of pharmaceutical industry, drug development and regulatory processes
Experience developing all Clinical trial plans, including site management, risk assessment and mitigation strategies, recruitment and retention plans, trial budgets and program-level budgets
Leader with growth mindset, willing to learn from others, committed to mentoring others and dedicated to promoting psychological safety
Strong communication skills with ability to present to a variety of stakeholders and tailor message accordingly
Strong project management skills with ability to collaborate effectively cross-functionally and hold team and CRO members accountable to tight timelines and budgets
High sense of urgency and ability to proactively identify critical path items and develop contingency plans to mitigate risk to budget, quality, and/or timelines
Work comfortably in a fast-paced, dynamic work environment and embrace change

Job Responsibility

Accountable for overall management of multiple clinical trials
Serves as the central point of contact and contributes expertise for clinical trial execution on assigned protocols
Works cross-functionally to establish and ensure clinical program timelines and goals are met and risks are appropriately escalated to Clinical Management. Ensures accurate tracking and reporting (dashboard) of study metrics and progress of study through completion
Leads the Clinical Study Team (CST) and may participate in other cross functional program team meetings
Ensures trial adherence to ICH/GCP/Federal and local regulations and company specific SOPs
Responsible for preparing and/or presenting to executive management as delegated
Develops, reviews and/or consults on clinical trial documents, such as study specific plans, informed consent, clinical protocols, Investigator Brochure, CSRs, yearly updates to the regulatory authorities and status updates
May be responsible for participating and presenting at Investigator Meetings, SIVs and other program meetings
Responsible for study level clinical operations budget forecasting, accrual management and quarterly review ensuring tight control between study forecasts and actuals
In conjunction with key stakeholders, oversee and manage the execution and filing of site clinical trial agreements, review of fair market value, CRO and vendor contracts, NDAs, etc

What we offer

A great culture, grounded in our C.O.R.E. values: Caring, Original, Resilient and Egoless
Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly
Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
We provide competitive time off, including three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
Commitment to growing you professionally and providing access to resources to further your development
Apogee offers regular all team, in-person meetings to build relationships and problem solve

Fulltime

Senior Manager, Site Engagement, Sponsor Dedicated

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

United States , LOS ANGELES, COLORADO, CALIFORNIA, ARIZONA, WASHINGTON

Salary:

133736.00 - 167170.00 USD / Year

iconplc

Expiration Date

Until further notice

Requirements

Detailed understanding of all aspects of clinical protocol design and implementation, clinical site monitoring as well as overall global drug development
Expert knowledge of clinical development (principles and concepts as well as regulatory environment e.g. ICH GCP and applicable regional/local regulations)
Oncology and/or Neurology and/or Immunology TA experience desired
Substantial (8+ years) experience in clinical operations in a CRO, pharma or biotech company including site management/oversight, and site-level clinical study conduct
Strong communication skills (verbal, written and listening) in both native language and English
Aptitude to interpret and to integrate site performance data in prioritization of oversight activities
Ensuring compliance with applicable T&E Policy requirements
Role requires domestic and international travel up to 50% of time
Ability to work independently on assigned tasks or projects of increasing complexity
Capability to perform self-training incl. on therapeutic area, and synthesize the key take-away points for studies under remit

Job Responsibility

Establish and manage site relationships
Act as liaison between the company and investigational sites, building investigator and site staff awareness on client compounds
Develop and implement a plan, in collaboration with global and local teams, to raise the profile of the company and its global clinical development projects with current and potential investigators
Independently perform activities associated with the evaluation of investigational sites to build company network
Proactively work with Medical/Patient/Industry Associations to build company network and to promote company clinical trials
Develop knowledge of site capabilities and past performance to assess their potential as participating sites in client clinical trials
Ensure regular communication with local organization to align interactions with KTLs and other relevant local/regional stakeholders
Oversee site-level study start-up, conduct, and close-out activities outsourced to CRO(s) for global programs across Therapeutic Areas
Support Site Agreement negotiations, including stand-alone and Master Site Agreements
Identify trends, issues and risks across sites, and work with external vendors and internal Trial Team to resolve/mitigate those

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

New

Marketing Communications Specialist

We are looking for a Marketing Communications Specialist to join our manufacturi...

Location

United States , Eagan

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Hands-on experience using Adobe Illustrator for marketing or graphic design projects
Working knowledge of design terminology, including file formats, sizing standards, and high-resolution asset requirements
Proficiency in developing social media graphics and related digital content using Canva and Adobe Photoshop
Experience creating video content, including editing work completed in Adobe Premiere Pro
Understanding of graphic design principles and how to translate ideas into effective visual assets
Background in project coordination or marketing support, including brief development and deadline management
Strong proofreading and organizational skills with careful attention to detail

Job Responsibility

Develop visually compelling social media content and supporting graphics that align with campaign goals and brand standards
Create and refine marketing materials using design tools such as Adobe Illustrator, Canva, and Adobe Photoshop
Produce and edit short-form video content to strengthen digital engagement and expand brand visibility
Prepare creative briefs and organize project inputs so design and content requests are clearly defined from the start
Coordinate the delivery of artwork, copy, and other assets to support timely production of marketing materials
Review content and layouts for quality, consistency, and accuracy before release or publication
Track milestones and follow up with stakeholders to help ensure deadlines are met across multiple marketing projects
Apply knowledge of file specifications, image resolution, and format requirements when preparing assets for print and digital use

What we offer

medical, vision, dental, and life and disability insurance
401(k) plan

Fulltime

New

SAP ABAP BTP Developer

You will be a key technical expert responsible for the core of our global B2B e-...

Location

India , Bangalore

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

5+ years of professional experience in ABAP development
Proven, hands-on proficiency in Object-Oriented ABAP
Extensive experience in developing OData services and REST/HTTP services on the SAP NetWeaver Gateway
Deep functional understanding of SAP Sales & Distribution (SD) module, specifically related to B2B sales processes (e.g., order-to-cash, pricing conditions, contracts)
Practical experience working in an agile environment (Scrum/Kanban) and using corresponding tools like JIRA and Confluence
Excellent communication and interpersonal skills, with fluency in English

Job Responsibility

Design and Develop APIs: Architect, create, and enhance mission-critical OData and RESTful services using the SAP NetWeaver Gateway
Build Robust Business Logic: Implement complex business processes (e.g., pricing, availability checks, order creation) using modern, Object-Oriented ABAP, ensuring code is clean, reusable, and performant
Integrate Core SAP Processes: Leverage your knowledge of BAPIs, IDocs, and other standard SAP interfaces to seamlessly connect our e-commerce layer with core ERP functionalities in Sales & Distribution (SD) and CRM
Ensure System Connectivity: Play a vital role in managing and developing interfaces between our on-premise SAP systems and various cloud solutions, utilizing tools like the SAP Business Technology Platform (BTP) and its connectivity services
Guarantee Quality and Stability: Champion development best practices, including writing automated tests (e.g., ABAP Unit) and participating in code reviews to maintain a high-quality, stable, and scalable platform
Collaborate and Orchestrate: Act as a technical liaison between business stakeholders, frontend developers, and external service providers to translate business requirements into effective technical solutions

New

Team Assistant

Are you an organised and proactive professional? Do you thrive in dynamic enviro...

Location

United Kingdom , Birmingham

Salary:

Not provided

Office Angels

Expiration Date

Until further notice

Requirements

Proven experience operating in a senior administrative or PA role within a fast-paced environment
Strong experience in minute taking, with the ability to accurately capture key discussions, actions, and decisions
Exceptional attention to detail, ensuring accuracy across all tasks and documentation
Excellent organisational skills, with the ability to manage multiple priorities effectively
Demonstrated ability to prioritise workload and meet tight deadlines in a high-pressure setting

Job Responsibility

Attend a high volume of internal and external meetings, taking clear, accurate, and concise minutes
Proactively manage complex and ever-changing diaries for senior stakeholders
Ensure all meetings are well-prepared with agendas, materials, and logistics in place
Provide comprehensive administrative support including document preparation, formatting, and correspondence
Plan and coordinate meetings, events, and business activities end-to-end
Liaise with internal teams and external partners to ensure smooth running of operations
Act as a key point of contact on behalf of senior leadership
Build strong relationships across the business and with external contacts
Communicate clearly and confidently at all levels

What we offer

Stunning offices with excellent public transport links
Immediate start available

Fulltime

New

Assistant Director Of Food & Beverage

Location

United States

Salary:

Not provided

Marriott Bonvoy

Expiration Date

June 23, 2026

Requirements

Bachelor’s degree in Hospitality Management, Business Administration, or related field preferred
Minimum of 5–7 years of progressive food and beverage leadership experience in a full-service or luxury hotel environment
Experience managing multiple outlets and large-scale banquet or convention operations required
Strong financial acumen with experience managing budgets, forecasting, and P&L performance
Proven leadership skills with the ability to inspire and develop teams
Excellent communication, organizational, and problem-solving abilities
Knowledge of Marriott systems and brand standards preferred
Ability to work a flexible schedule, including evenings, weekends, and holidays

Job Responsibility

Assist in the overall management and leadership of all food and beverage outlets, including restaurants, lounges, in-room dining, banquets, and special event venues
Support large-scale operations including convention center programming and amphitheater events, ensuring seamless execution and guest satisfaction
Partner with the Director of Food & Beverage to develop and implement strategic initiatives to drive revenue, profitability, and guest engagement
Ensure compliance with Marriott Autograph Collection standards, local regulations, and health and safety requirements
Lead, coach, and develop department managers and team members
promote a culture of accountability, engagement, and continuous improvement
Oversee scheduling, labor management, and productivity to meet financial targets
Monitor financial performance, including revenue, cost of goods sold, labor expenses, and overall profitability
take corrective action as needed
Collaborate with Culinary, Sales, and Events teams to execute group business, catering events, and activations at the highest level

What we offer

Medical, Dental, & Vision
HSA & Flexible Spending Account Options
Basic Life & Disability Plan Options
401K Retirement Plan
Paid Time Off
Holiday Pay
Career Training & Development Opportunities
Tuition Reimbursement
Bereavement Leave
Employee Assistant Program (EAP)

Fulltime

New

Medical Receptionist

We are looking for a detail-oriented Medical Receptionist to support daily front...

Location

United States , Rochester

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Previous experience in a medical front office, reception, or similar patient-facing administrative role
Working knowledge of patient scheduling practices and front-desk coordination
Ability to perform patient check-in tasks accurately and maintain organized records
Familiarity with basic medical terminology used in a healthcare setting
Strong communication skills with a detail-oriented and welcoming approach to patient service
Ability to manage multiple tasks efficiently in a fast-paced office environment

Job Responsibility

Welcome patients and visitors in a courteous manner and guide them through the arrival process
Coordinate appointment calendars, schedule patient visits, and update reservations as needed
Manage front-office communications by answering calls, relaying messages, and responding to routine inquiries
Handle patient check-in activities, confirm essential information, and maintain accurate reception records
Support administrative office functions such as preparing forms, organizing documents, and assisting with daily workflow
Use basic medical terminology appropriately when communicating with patients and healthcare team members

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Fulltime

Program Manager, Clinical Data Science, Sponsor Dedicated

iconplc

Location:
United States

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 25, 2026

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