Federated Registry Program Coordinator

Rhythm Pharmaceuticals, Inc; Netherlands; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Home office based

Hybrid work model with international旅行

Job summary

Rhythm Pharmaceuticals, Inc in the Netherlands is seeking a detail-oriented projects coordinator to support the federated registries program. You will organize governance meetings, manage documentation, and coordinate multiple stakeholders across internal teams, experts, and vendors.

This home-office based role offers hybrid work, international travel, and opportunities to contribute to governance, data-sharing documentation, and onboarding of new registries.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Prior experience in project coordination, clinical research operations, registry coordination, medical affairs, or a healthcare environment preferred.
• Strong organizational and coordination skills with the ability to manage multiple workstreams, timelines, documents and stakeholders.
• Able to support administrative and contractual processes.
• Strong communication and interpersonal skills, capable of engaging with senior leadership and key stakeholders.

Responsibilities

• Organize governance meetings, including invitations, agendas, minutes, and action-item follow-up.
• Support contractual and administrative activities, including letters of intent, agreements, data-sharing documentation, and any other key documentation.
• Coordinate consensus-building activities, including expert meetings, surveys, Delphi rounds, documentation, and stakeholder follow-up.
• Support operational and administrative coordination for the federated registry.
• Manage scientific publications’ related administrative activities, including conflict-of-interest disclosures, author documentation, and timeline tracking.
• Support the expansion of the registry network by coordinating onboarding activities for new registries.
• Coordinate crosswalk activities and documentation requirements for new participating registries or sites before submission to the scientific committees.
• Maintain project trackers, timelines, and other key program documentation to ensure effective program execution.

Skills

Project coordination

Clinical research operations

Registry coordination

Communication skills

English fluency

Education

Bachelor’s degree in life sciences or related field

Job description

Company Overview

Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to learn, adapt, and our tenacity to overcome barriers, together.

Opportunity Overview

This role will support the coordination and operational management of a federated registries program focused on rare diseases. The coordinator will contribute to the execution of program activities by supporting governance, administrative and contractual activities, data collection and analysis workflows, and the onboarding of new centers and registries. The role requires strong organizational skills, attention to detail, and the ability to coordinate multiple stakeholders internal teams, external experts, and vendors.

Responsibilities & Duties

• Organize governance meetings, including invitations, agendas, minutes, and action-item follow-up


• Support contractual and administrative activities, including letters of intent, agreements, data-sharing documentation, and any other key documentation


• Coordinate consensus-building activities, including expert meetings, surveys, Delphi rounds, documentation, and stakeholder follow-up


• Support operational and administrative coordination for the federated registry


• Manage scientific publications’ related administrative activities, including conflict-of-interest disclosures, author documentation, and timeline tracking


• Support the expansion of the registry network by coordinating onboarding activities for new registries


• Coordinate crosswalk activities and documentation requirements for new participating registries or sites before submission to the scientific committees


• Maintain project trackers, timelines, and other key program documentation to ensure effective program execution

Qualifications & Skills

• Bachelor’s degree, degree in life sciences, or project management, or any related field


• Prior experience in project coordination, clinical research operations, registry coordination, medical affairs, or a healthcare environment preferred


• Strong organizational and coordination skills, with the ability to manage multiple workstreams, timelines, documents, and stakeholders


• Able to support administrative and contractual processes


• Strong communication and interpersonal skills, capable of engaging with senior leadership and key stakeholders.


• Not accepting the status quo, working with a sense of urgency to deliver results


• Self-starter mentality who feels comfortable working in a fast-paced environment


• Cross-functional mindset focused on a seamless collaboration with internal and external partners


• Fluent in English

This role is home office based.

Rhythm operates in a hybrid-work model. Candidates applying must be willing and able travel internationally.

More about Rhythm

We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare melanocortin-4 receptor (MC4R) pathway diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.

Our Core Values

We are committed to advancing scientific understanding to improve patients’ lives

We are inspired to tackle tough challenges and have the courage to ask bold questions

We are eager to learn and adapt

We believe collaboration and ownership are foundational for our success

We value the unique contribution each individual brings to furthering our mission.

Inherent in our core values is the commitment to act ethically and with integrity in all we do.