Regulatory affairs lead Work, Jobs in Tipton, Wmd (with Salaries)

Scientific Affairs Manager, UK - Birmingham
Rhythm Pharmaceuticals —Birmingham
- Full-time
- Doctoral degree
- Presentation skills
- Communication skills
Sr Manager Regulatory and Clinical Affairs
Thermo Fisher Scientific —Birmingham
- Full-time
- Management
- Bachelor's degree
- Travel
Product Lead - XDI
Company: ArisGlobal —Wolverhampton
- Product management
- AI
- Communication skills
International Recruitment Operations Manager
University of Worcester —Worcester
- £31,236 - £37,694 a year
- Full-time
- Databases
- University
- Continuous improvement
- Employee assistance programme
6d
Finance Schemes & Reporting Partner
Low Carbon Contracts Company —Birmingham
- £72,000 a year
- Full-time
- Hybrid work
- Writing skills
- Communication skills
- Annual leave
- Work from home
Quick apply
2d

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Sr Manager Regulatory and Clinical Affairs
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Scientific Affairs Manager, UK - Birmingham

Rhythm Pharmaceuticals
Birmingham

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Job details

Full-time

Qualifications

Clinical research
Doctoral degree
Stakeholder collaboration
Stakeholder liaison
Internal department liaison
Presentation skills
Partnership building
Multidisciplinary collaboration
Pharmaceutical industry setting experience
Cross-functional collaboration
Medical affairs
Communication skills
Cross-functional communication

Full 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 adapt, learn, and our tenacity to overcome barriers, together.

Job Summary
As a member of the Rhythm UK & Ireland team, you will focus on advancing medical and scientific initiatives in rare MC4R pathway diseases. In close collaboration with the national and international Medical Affairs teams, the Scientific Affairs Manager (SAM) will provide scientific and medical leadership and support for the implementation of integrated tactical and engagement plans, while upholding the highest standards of compliance and scientific integrity in the UK.
He/she will be responsible for building peer to peer relationships with Key External Experts (KEEs) and other stakeholders to deliver clinical, scientific, and medical education. The SAM will support research initiatives, advisory boards, and other compliant scientific exchange activities to support the integrated strategic and tactical plan and the Medical Affairs’ tactics.

Responsibilities and Duties

Serve as a Scientific Affairs Manager for the UK and as a member of the international Medical Affairs team.
Be a subject-matter expert for the MC4R pathway diseases and our indications.
Contribute to the development and implement of the integrated strategic and tactical plan with focus on the medical and scientific projects and tactics.
Organize and lead local advisory boards and Key External Expert meetings to gain insights, foster scientific exchange and support the local strategy.
Provide medical support for the implementation of the local strategy.
Build and maintain peer-to-peer relationships with external experts and stakeholders, delivering clinical, scientific, and medical education.
Oversee and initiate medical projects in collaboration with clinical partners and research networks.
Identify stakeholder and provide insights for future clinical developments and play a key role in the pre-launch and launch phase for these new developments.
Contribute to the development and implementation of scientific communication plans and medical information materials, ensuring compliance with local regulatory requirements.
Collaborate closely with Drug Safety, Market Access, and Commercial.
Collaborate with the clinical team and monitor all Rhythm clinical trials taking place in the UK and follow up where necessary.
Identify knowledge gaps among healthcare professionals and organize non-promotional scientific presentations.
Participate in local medical and cross-functional projects and initiatives.
Ensure effective and compliant communication with internal and external stakeholders.
Support the commercial team and HCPs with knowledge building around the efficacy and safety of setmelanotide, including AE/PV reporting.
Play a pivotal role in establishing appropriate multidisciplinary care including patient support programs.
Play a pivotal role in identifying hurdles and solutions in order to optimize patient identification and referral pathways.
Respond to unsolicited requests for medical information in a timely manner. Ensure that an accurate and fair-balanced response is provided.

Qualifications and Skills

Advanced degree in a pharmaceutical, scientific, or medical field (PharmD, PhD, MD)
8 or more years’ experience within a Medical Science Liaison or similar field facing role with primary emphasis on field based scientific exchange within the biopharmaceutical industry. Relevant pharmaceutical and clinical/therapeutic experience also a consideration
Rare diseases experience is a plus
Launch experience is a plus
Proven skills and ability to work in a cross-functional team without silos
Cross-functional mindset focused on a seamless collaboration with the commercial team
Not accepting the status quo, working with a sense of urgency to deliver results
Self-starter mentality who feels comfortable to work in a fast paced environment
Excellent communication skills and scientific acumen when presenting clinical, disease state information to a variety of audiences
Demonstrates knowledge of regional/local specific healthcare systems, the evolving medical landscape, reimbursement and industry trends.

This role will be home-office based. Candidates applying must be based in a centralized UK location and have easy access to transportation and airports.

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 neuroendocrine 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.

At Rhythm our core values are:

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.

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regulatory affairs lead jobs in tipton, wmd

Scientific Affairs Manager, UK - Birmingham

Sr Manager Regulatory and Clinical Affairs

Product Lead - XDI

International Recruitment Operations Manager

Finance Schemes & Reporting Partner

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