Pharma IT is hiring Senior & Principal Clinical Project Management Consultants to join our Clinical Science & Trial Operations Team!
In this role, you will work as a consultant to support our clients in the Pharma, Biotech and Medical Device industries.
In this position, you will work on-site at the client’s location or remote with the support of the rest of the Clinical Science & Trial Operations team, when you need it.
The ideal candidate will have experience from different biotech and pharma companies working with clinical development in different indications.
As a Senior/Principal Clinical Project Manager Consultant, you will:
- Lead the development and execution of clinical projects, from initiation to closure, ensuring adherence to project timelines, budget, and scope.
- Collaborate with cross-functional teams, including external stakeholders, to ensure project goals, deliverables, and requirements.
- Develop comprehensive project plans, including outsourcing plans, risk management, sponsor oversight and communication strategies.
- Foster effective communication and collaboration among project team members, ensuring clarity of roles and responsibilities.
- Ensure compliance with regulatory requirements and industry standards throughout the project lifecycle.
- Evaluate project outcomes and provide recommendations for process improvements and best practices.
The ideal candidate for this position holds the following qualifications:
- Bachelor’s, Master´s or PhD degree in relevant field
- 10+ years of experience from various clinical trials in pharma and biotech industry
- Experience with First in Human Trials
- Strong understanding of clinical research methodologies, regulations, and quality standards.
- Proven track record of successfully managing complex clinical projects within budget and timeline constraints.
- Excellent leadership and interpersonal skills, with the ability to collaborate effectively with multidisciplinary teams.
- Exceptional problem-solving and decision-making abilities, with a focus on achieving results.
- Excellent written and verbal communication skills in English, with the ability to present complex information to diverse audiences.
About Our Firm
Pharma IT is a certified Great Place to Work. We aim to deliver price-competitive young talent and experienced professional consultants to the pharma, biotech, and medical device industries. Our exclusive focus on these industries and agile, customer-oriented approach ensures we maximize customer value.
We assist clients across all key areas of these industries, including: Management & Business Consulting, IT Consulting, Drug Development, Medical Device Consulting, Manufacturing Consulting, Quality, Compliance & Security Consulting.
Our team consists of ~140 diverse and talented consultants, and we are currently experiencing rapid growth. We encourage people of all ages, genders, sexual orientations, nationalities, religions, and ethnic backgrounds, to apply. If you want to know more about us, feel free to check out our website at pharmait.dk
You can learn more about Pharma IT’s Clinical Science & Trial Operations Team, here: https://pharmait.dk/services/drug-development/clinical-science-and-trial-operations/
Benefits
Pharma IT is a certified Great Place to Work, with industry-leading contracts and work-life balance. We offer a base salary with an accelerated bonus model as part of what we believe is one of the best employment packages in the industry. Our core belief is that employees should have flexible hours, do what they are best at, and be able to spend as much time at our customers’ sites as possible.
How to Apply
This position will be filled on a rolling basis. Interested applicants should apply via LinkedIn. If you have any questions about this role, feel free to reach out to the hiring manager for this position, Director Trine Stougaard Bak at trst@pharmait.dk
