Hi, I'm Ida Bisbo. With a background in pharmaceutical design and engineering, and hands-on experience in clinical trials, digital collaboration, and AI data training, I bring a unique blend of scientific expertise and digital marketing savvy. I enjoy managing projects, improving processes, and crafting engaging content to support innovative brands. Currently, I work as a freelance social media manager, paid ads strategist, and website designer, while also contributing to AI innovation as a content writer and data trainer. My passion for learning and adaptability makes me thrive in international, interdisciplinary teams. In my previous roles, I've successfully coordinated clinical trials at Novo Nordisk and led digital initiatives to enhance collaboration and efficiency. My strong communication and project management skills have helped train colleagues, execute campaigns, and streamline regulatory data management. I’m always eager to connect, grow my network, and contribute to meaningful projects in life sciences and digital marketing.

Ida Bisbo

Hi, I'm Ida Bisbo. With a background in pharmaceutical design and engineering, and hands-on experience in clinical trials, digital collaboration, and AI data training, I bring a unique blend of scientific expertise and digital marketing savvy. I enjoy managing projects, improving processes, and crafting engaging content to support innovative brands. Currently, I work as a freelance social media manager, paid ads strategist, and website designer, while also contributing to AI innovation as a content writer and data trainer. My passion for learning and adaptability makes me thrive in international, interdisciplinary teams. In my previous roles, I've successfully coordinated clinical trials at Novo Nordisk and led digital initiatives to enhance collaboration and efficiency. My strong communication and project management skills have helped train colleagues, execute campaigns, and streamline regulatory data management. I’m always eager to connect, grow my network, and contribute to meaningful projects in life sciences and digital marketing.

Available to hire

Hi, I’m Ida Bisbo. With a background in pharmaceutical design and engineering, and hands-on experience in clinical trials, digital collaboration, and AI data training, I bring a unique blend of scientific expertise and digital marketing savvy. I enjoy managing projects, improving processes, and crafting engaging content to support innovative brands. Currently, I work as a freelance social media manager, paid ads strategist, and website designer, while also contributing to AI innovation as a content writer and data trainer. My passion for learning and adaptability makes me thrive in international, interdisciplinary teams.

In my previous roles, I’ve successfully coordinated clinical trials at Novo Nordisk and led digital initiatives to enhance collaboration and efficiency. My strong communication and project management skills have helped train colleagues, execute campaigns, and streamline regulatory data management. I’m always eager to connect, grow my network, and contribute to meaningful projects in life sciences and digital marketing.

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Experience Level

Intermediate
Intermediate
Intermediate
Intermediate

Language

Danish
Fluent
English
Fluent
German
Intermediate

Work Experience

Freelance SoMe Manager | Paid Ads & SEO Strategist | Website Designer
March 1, 2025 - Present
Plan, execute, and optimize paid advertising campaigns on Meta, including A/B testing, audience targeting, and budget management. Monitor and analyze campaign performance using Meta Pixel, tracking conversions, refine strategies, and improve Return on Ad Spend. Develop and implement content strategies for Meta and LinkedIn to support brand growth and marketing objectives. Create, edit, and publish engaging content across platforms and websites to boost visibility, reach, and engagement. Edit and manage website content, including writing and publishing blog posts, including SEO optimization.
Content Writer & AI Data Trainer at Outlier, DataAnnotation & DataForce
October 1, 2024 - Present
Contribute through a best-in-class remote platform, supporting AI innovation with reliable, transparent, and flexible workflows. Specialize in evaluating, fact-checking, and refining outputs for large language models. Write, edit, and optimize website pages, blog posts, emails, and social media content. Provide Danish copy review and translations, drawing on experience from a previous copywriting client project. Ensure consistency and clarity by proofreading and refining content across platforms. Freelance consultant providing expert human feedback to improve AI-generated responses.
Global Clinical Trial Administrator | Rare Diseases at Novo Nordisk
March 31, 2025 - July 20, 2025
Coordinated Phase 1-3 trials and clinical IT systems, including Trial Master File. Prepared trial documents (submissions, contracts, translations) and managed communication tools (mailboxes, calendars, newsletters). Led a Digital Playbook initiative, focusing on aligning clinical trial processes, expanding from Rare Disease to three additional areas, improving digital collaboration skills. Led an 8-member digital collaboration team and facilitated a cross-functional group of 11 stakeholders to enhance Playbook implementation across Novo Nordisk. Trained 50+ colleagues in Digital Playbook, improving collaboration on clinical trials. Designed workshops and executed a hybrid Playbook campaign engaging 100+ employees. Enhanced project management, communication, and regulatory skills, driving innovative process improvements and implementations.
Junior Project Manager | Life Science Consultant at Genau & More
April 30, 2024 - July 20, 2025
Led an IT & Automation project to update 11 production line servers. Orchestrated project lifecycle from Initiate through Planning to Execution phase. Performed server validation and qualification, ensuring all documentation, including SOPs, were updated in Veeva Vault QualityDocs. Strengthened project and stakeholder management skills, technical expertise, and ensured compliance with GMP, GAMP5, and GxP standards.
Regulatory Affairs Data Management | Student Assistant at LEO Pharma
July 31, 2023 - July 20, 2025
Worked with regulatory data management for drug submissions and market authorizations. Maintained the global regulatory GxP data model for LEO Pharma products, strengthening regulatory expertise. Contributed to the migration of all regulatory data from the outdated eRIM system to Veeva Vault RIM, including go-live and hyper-care support. Led recruitment and onboarding of student assistants into the department. Enhanced data management and migration skills, focused on operational improvements.
Internship | Research Project at Bactolife
May 31, 2022 - July 20, 2025
Contributed to start-up efforts by developing SOPs and supporting lab equipment procurement. Conducted research to optimize single-domain antibody expression as an alternative to antibiotics in a biotech start-up. Enhanced leadership, technical expertise, and adaptability in fast-paced environments.
Project & Program Management, Global IT | Student Assistant at LEO Pharma
June 30, 2021 - July 20, 2025
Orchestrated workshops in the commercial area, providing support to Programme Area Leaders, project managers, stakeholders, and SCRUM masters for effective project and portfolio execution. Defined internal PMO processes and actively participated in Stage Gate meetings to ensure project alignment and success. Supported organizational transformation to Agile project management, fostering adaptability and efficiency.
Project Office & IT | Student Assistant at Novo Nordisk Pharmatech
August 31, 2019 - July 20, 2025
Collaborated with project managers and stakeholders on IT, supply chain, and data management projects, ensuring efficient project execution. Developed an Excel-based resource tracking tool to monitor and manage FTEs on projects, resulting in an 18% reduction in resource allocation across all IT projects in the department. Led workshops and supported Stage-gate meetings, driving project alignment and progress and ensuring timely milestones.

Education

Master in Science Engineering at Technial University of Denmark
September 1, 2017 - July 1, 2022
M.Sc at Technical University of Denmark
January 1, 2021 - July 31, 2023
B.Sc at Technical University of Denmark
September 1, 2017 - December 31, 2020

Qualifications

Clinical Development and Applied Good Clinical Practice (GCP)
January 1, 2024 - December 31, 2024
Validation & Qualification Course
January 1, 2023 - December 31, 2023
SmartGMP Basic & Intermediate Pharmaceutical Production
January 1, 2023 - December 31, 2023
ISO 21500 Guidance on Project Management
January 1, 2021 - December 31, 2021
Skin Care & Repair
January 1, 2025 - December 31, 2025

Industry Experience

Life Sciences, Healthcare, Manufacturing, Professional Services, Software & Internet