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Customer Service Jobs in Ocoee, FL

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Global Medical Affairs Lead, PDT Immunology (Director) Takeda Pharmaceutical Co Ltd

Cambridge, MA

$192,400–$302,390 / year

Desirable: Demonstrated curiosity and working knowledge of artificial intelligence, digital health, real-world evidence, data analytics, device innovation, and other technology-enabled advances that can improve medical decision-making, education, and patient outcomes. Support design and execution of designated evidence generation led by Medical Affairs, including Phase IIIb/IV studies, disease registries, observational studies, and noninterventional research, in collaboration with Therapeutic Area Unit representatives and Global Clinical Operations.

30+ days ago

Senior Director, Regulatory Affairs CMC – Small Molecule Beeline Medicines

Cambridge, Massachusetts

$242,000–$313,500 / year

Act as a fully integrated partner within the CMC team, attending key technical meetings, engaging daily with Process Development, Analytical, Manufacturing Sciences, Drug Supply and Quality colleagues, and translating regulatory strategy into practical guidance that enables the CMC team to make informed decisions and move programs forward with regulatory confidence. Demonstrate entrepreneurial drive and resourcefulness in executing CMC regulatory responsibilities — proactively seek out information, build relationships across the CMC organization, and find creative avenues to get things done; a successful CMC regulatory lead takes ownership of being plugged in, earns trust within the team, and removes barriers through initiative and ownership.

6 days ago

Senior Director, Regulatory Affairs CMC – Biologics Beeline Medicines

Cambridge, Massachusetts

$242,000–$313,500 / year

Demonstrate entrepreneurial drive and resourcefulness in executing CMC regulatory responsibilities — proactively seek out information, build relationships across the CMC organization, and find creative avenues to get things done; a successful CMC regulatory lead takes ownership of being plugged in, earns trust within the team, and removes barriers through initiative and ownership. Act as a fully integrated partner within the CMC team, attending key technical meetings, engaging daily with Process Development, Analytical, Manufacturing Sciences, Drug Supply and Quality colleagues, and translating regulatory strategy into practical guidance that enables the CMC team to make informed decisions and move programs forward with regulatory confidence.

6 days ago

Assistant Professor Faculty Positions in the Department of City Planning and Urban Affairs, with a focus on Livable and Resilient Cities Boston University

Boston, MA

$105,000–$115,000
Full time

Applicants should provide a personal statement that describes the candidate’s interest in both the convergent area of Livable and Resilient Cities and the department; curriculum vitae; a research statement describing their research interests and experience;a teaching and mentoring statement detailing their approach to teaching and mentoring in an inclusive and diverse learning environment; and the names and contact information of 3 references at https://academicjobsonline.org/ajo/jobs/32948 . The salary allocated for these roles is $105,000 to$115,000.Final salary determination and rank placement will be based on the candidate's academic record, research background, years of qualifying experience, and a variety of other factors, including but not limited to licenses, specialty, departmental budgets, training and internal pay comparison.

1 day ago

Medical Director of Clinical Affairs - Remote Included Health

Boston, MA

Remote

They will translate population health data into actionable clinical campaigns, clinically steer multi-vendor ecosystems (including TPAs and carriers), and collaborate with internal business strategy teams to scale repeatable clinical solutions in the market. Starting base salary for you will depend on several job-related factors, unique to each candidate, which may include education; training; skills; years and depth of experience; certifications and licensure; our needs; internal peer equity; organizational considerations; and understanding of geographic and market data.

20 days ago

Director, Regulatory Affairs Sumitomo Pharma America Holdings Inc (Inactive)

Marlborough, MA

$195,900–$244,900 / year

Assist with development of the global regulatory functional plan through research, review and interpretation of related product approvals, current regulatory guidance documents and recent public Advisory Committee proceedings to support the successful submission and achievement of target product labeling. Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS.

9 days ago

Senior Director, State Government Affairs Beam Therapeutics Inc

Cambridge, MA

$260,000–$320,000 / year

Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This individual will be responsible for building a variety of strong, meaningful networks at the state level (including State Medicaid officials, state legislators and state policy stakeholders) and staying current on critical policy issues.

30+ days ago

Provost and Vice President for Academic Affairs Bridgewater State University

Bridgewater, MA

$275,000–$325,000 / year

This position works collaboratively with highly committed faculty, librarians, deans, and staff to ensure the quality and integrity of academic programs; coordinates the development of new and innovative programs; secures relevant accreditations; leads the recruitment and development of faculty; promotes innovation and excellence in teaching, scholarship, research, creative pursuits and service; and leads the division's strategic planning efforts. From being named one of the Best Colleges in America by The Wall Street Journal for a third consecutive year, being ranked the 3rd safest campus and the 3rd most LGBTQ+ Friendly College in the U.S., to our nationally leading undergraduate research program, our ranking as the #1 driver of social mobility among more than 100 colleges and universities in Massachusetts, Bridgewater State University has emerged as the flagship of the state university system.

30+ days ago

Director Regulatory Affairs Business Development AbbVie Inc

Cambridge, MA

This role supports regulatory activities associated with business transactions including in-licensing and out-licensing, co-development/collaborations, acquisitions of new chemical or molecular entities including advanced, tissue, and cell-based therapies, platform technologies, marketed products, and company acquisitions to further the company's overall strategic business development objectives. Responsible for preparing oral and written regulatory scientific assessments for potential in-license/out-license, R&D co-development/collaborations and all company or asset acquisitions based on face-to-face and virtual meetings with external companies/representatives, and confidential and public data review for identified compounds, companies, or entities.

3 days ago

Director, Regulatory Affairs Business Development AbbVie

Cambridge, Massachusetts

$182,000–$346,000
Full time

This role supports regulatory activities associated with business transactions including in-licensing and out-licensing, co-development/collaborations, acquisitions of new chemical or molecular entities including advanced, tissue, and cell-based therapies, platform technologies, marketed products, and company acquisitions to further the company’s overall strategic business development objectives. Responsible for preparing oral and written regulatory scientific assessments for potential in-license/out-license, R&D co-development/collaborations and all company or asset acquisitions based on face-to-face and virtual meetings with external companies/representatives, and confidential and public data review for identified compounds, companies, or entities.

4 days ago

Senior Director, State Government Affairs Beam Therapeutics

Cambridge, MA

$260,000–$320,000 / year

Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This individual will be responsible for building a variety of strong, meaningful networks at the state level (including State Medicaid officials, state legislators and state policy stakeholders) and staying current on critical policy issues.

30+ days ago

Regulatory Affairs Manager Medtronic Plc

Mansfield, MA

If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program).

10 days ago

Executive Director, Medical Affairs Operations & Strategic Excellence Viridian Therapeutics Inc

Waltham, MA

This individual will facilitate a broad range of strategic and tactical initiatives across all functional areas, including Independent Medical Education (IME), Investigator-Sponsored Trials (ISTs), Medical Communications, Medical Information, Health Economics and Outcomes Research (HEOR), Expanded Access Programs (EAP), and the field medical team. This role will focus on refining the medical affairs strategy, scientific platform and key messaging; enhancing training programs; contracting with vendors to implement platforms and services; ensuring policies and procedures are in place and being followed; supporting key opinion leader (KOL) engagement initiatives, and reporting on KPIs.

25 days ago

Clinical Affairs Director Philips

Cambridge, MA

$171,000–$273,000 / year

Direct cross-functional collaboration among Clinical Affairs, R&D, Regulatory Affairs, Medical Affairs, Marketing, and external stakeholders to ensure strategic alignment and successful execution of clinical initiatives. The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.

17 days ago

Medical Affairs/Safety - Associate Director, Patient Advocacy and Engagement TalentBurst, Inc.

Cambridge, MA

$60–$83.74 / hour
Quick Apply

The Associate Director, Patient Advocacy and Engagement, Rare and Pipeline will play a critical role in driving patient-centric strategies and strengthening relationships with patient advocacy organizations primarily in US. Develop initiatives to enhance disease awareness and improve time to diagnosis, as well as educate the patient community so that they are empowered to actively engage with their healthcare provider in the management of their disease.

30+ days ago

Senior Account Executive, Public Relations Orchestra

Waltham, New York

Orchestra is committed to building and maintaining a diverse staff, and recognizes that its continued success depends on hiring and retaining high-quality creative professionals with a variety of backgrounds and experiences. Ability to communicate clearly, effectively and with confidence, both verbally and in writing, with varying levels of staff, clients and the media, and is comfortable thinking on their feet.

30+ days ago

Senior Account Executive, Public Relations Inkhouse

Waltham, New York

30+ days ago

Marketing & Public Relations Supervisor, Customer Energy Solutions (Hybrid Schedule) Eversource Energy

Westwood, MA

$121,080–$134,530 / year

Our Team/Role: The Marketing & Public Relations Supervisor is responsible for leading and executing public relations, media relations, thought leadership, industry association engagement, strategic events, and external outreach initiatives within the Energy Efficiency / Electric Mobility / Active Demand Response (EE/EV/ADR) department across the company's three operating states (Connecticut, Massachusetts, and New Hampshire). The Supervisor serves as the primary point of contact for EE/EV/ADR public relations and thought leadership initiatives and works closely with Eversource's Media Relations team, internal stakeholders, business and sales management, and internal and external marketing partners.

6 days ago

Part Time Lecturer - Regulatory Affairs (Boston) Northeastern University

Boston, MA

Northeastern University's College of Professional Studies is seeking part-time faculty to teach graduate-level, on-ground courses in Boston for the Master of Science in Regulatory Affairs program and its associated graduate certificates. Instructional areas include, but are not limited to, drug and biologics development, medical device regulations, clinical trial management, commercialization of medical products/technology, law and intellectual property, international regulatory affairs, and regulatory writing.

14 days ago

Director, Medical Affairs, Oncology -- Blue Earth Diagnostics Bracco SpA

Needham, MA

$200,000–$240,000 / year

Provide USMA representation and support across multiple company sponsored clinical trials / global development programs, including assisting and advising on investigator and site selection, liaising with KOLs/investigators, assisting with insight generation as required to support these initiatives. This individual will actively contribute to all aspects of new product support and play a critical role in promoting and maintaining professional relationships with key national and international medical experts, as well as supporting the field medical and patient advocacy teams in its initiatives.

23 days ago

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Customer Service Jobs in Ocoee, FL

Global Medical Affairs Lead, PDT Immunology (Director) Takeda Pharmaceutical Co Ltd

Senior Director, Regulatory Affairs CMC – Small Molecule Beeline Medicines

Senior Director, Regulatory Affairs CMC – Biologics Beeline Medicines

Assistant Professor Faculty Positions in the Department of City Planning and Urban Affairs, with a focus on Livable and Resilient Cities Boston University

Medical Director of Clinical Affairs - Remote Included Health

Director, Regulatory Affairs Sumitomo Pharma America Holdings Inc (Inactive)

Senior Director, State Government Affairs Beam Therapeutics Inc

Provost and Vice President for Academic Affairs Bridgewater State University

Director Regulatory Affairs Business Development AbbVie Inc

Director, Regulatory Affairs Business Development AbbVie

Senior Director, State Government Affairs Beam Therapeutics

Regulatory Affairs Manager Medtronic Plc

Executive Director, Medical Affairs Operations & Strategic Excellence Viridian Therapeutics Inc

Clinical Affairs Director Philips

Medical Affairs/Safety - Associate Director, Patient Advocacy and Engagement TalentBurst, Inc.

Senior Account Executive, Public Relations Orchestra

Senior Account Executive, Public Relations Inkhouse

Marketing & Public Relations Supervisor, Customer Energy Solutions (Hybrid Schedule) Eversource Energy

Part Time Lecturer - Regulatory Affairs (Boston) Northeastern University

Director, Medical Affairs, Oncology -- Blue Earth Diagnostics Bracco SpA

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