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Opera Director Jobs in Wakefield, MA (NOW HIRING)

Boston Conservatory

Costume Shop Intern

Boston, MA · On-site

$16.25 - $21.75/hr

... designers, directors, performers, and choreographers, to costume builds and alterations ... Opera are all worked on at Boston Conservatory at Berklee. Specifi c skills for stage costuming are ...

Berklee College of Music

Costume Shop Intern

Boston, MA · On-site

$16.25 - $21.75/hr

... designers, directors, performers, and choreographers, to costume builds and alterations ... Opera are all worked on at Boston Conservatory at Berklee. Specifi c skills for stage costuming are ...

mjh

Business Travel Sales Manager

Boston, MA · On-site

Director of Sales & Marketing Location: Cambria Hotel Boston Downtown Position Summary The Business ... Experience with Delphi, Opera, Salesforce, or similar CRM and PMS platforms

RAFFLES

Reservations Coordinator

Boston, MA · On-site

Support Director of Revenue in proactive and accurate maintenance and management of all systems: Opera PMS, ORS, Ideas RMS, OTA Extranets. * Champion relationship with GRC and ensure call center is ...

mjh

Business Travel Sales Manager

Boston, MA

Director of Sales & Marketing Location: Cambria Hotel Boston Downtown Position Summary The Business ... Experience with Delphi, Opera, Salesforce, or similar CRM and PMS platforms

AccorHotel

Reservations Coordinator

Boston, MA · On-site

$27.81 - $30.90/hr

Support Director of Revenue in proactive and accurate maintenance and management of all systems: Opera PMS, ORS, Ideas RMS, OTA Extranets. * Champion relationship with GRC and ensure call center is ...

AccorHotel

Reservations Coordinator

Boston, MA · On-site

$27.81 - $30.90/hr

Support Director of Revenue in proactive and accurate maintenance and management of all systems: Opera PMS, ORS, Ideas RMS, OTA Extranets. * Champion relationship with GRC and ensure call center is ...

AccorHotel

Reservations Coordinator

Boston, MA · On-site

$27.81 - $30.90/hr

Support Director of Revenue in proactive and accurate maintenance and management of all systems: Opera PMS, ORS, Ideas RMS, OTA Extranets. * Champion relationship with GRC and ensure call center is ...

AccorHotel

Accounting Generalist

Boston, MA

... Director of Finance and staff in maintaining accurate and timely financial reporting; ensuring ... Experience with the Opera/Opera Cloud PMS is preferred. ➢ Multitasking, working under pressure ...

New

mjh

Group Sales Manager

Boston, MA

Director of Sales & MarketingLocation: Boston, MA Position Summary The Group Sales Manager is ... Opera, Salesforce, or similar preferred)

mjh

Group Sales Manager

Boston, MA · On-site

Director of Sales & MarketingLocation: Boston, MA Position Summary The Group Sales Manager is ... Opera, Salesforce, or similar preferred)

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All JobsOpera JobsOpera Director JobsOpera Director Jobs in Wakefield, MA

Opera Director information

What does an opera director do?

An Opera Director is responsible for overseeing the artistic vision and staging of an opera production. They work closely with performers, designers, and conductors to bring the story to life through movement, characterization, and visual elements. Their role includes interpreting the score and libretto, guiding rehearsals, and ensuring cohesion between music and theatrical performance. Ultimately, they shape the overall audience experience by blending music, drama, and stagecraft.

What skills and qualifications are needed to thrive as an opera director?

To thrive as an Opera Director, you need a deep understanding of music, dramatic interpretation, and stagecraft, usually supported by formal training in theatre, music, or opera direction. Familiarity with score reading software, stage management systems, and sometimes union regulations is important for coordinating performances and rehearsals. Superior leadership, creativity, communication, and organizational skills help guide teams and bring artistic visions to life. These abilities are crucial for successfully navigating complex productions and ensuring cohesive, compelling performances.

What are the main challenges an opera director faces during a production?

Opera Directors often encounter the challenge of balancing artistic vision with the practical constraints of budgets, casting, and venue limitations. Coordinating large teams—including singers, musicians, designers, and technicians—requires strong leadership and communication throughout the rehearsal process. Successfully resolving creative differences and logistical issues while adhering to deadlines is a key part of the role. The ability to adapt and problem-solve on the fly ensures that both rehearsals and performances run smoothly, ultimately bringing the director’s vision to the stage.

How much does an opera director make?

Opera directors typically earn between $50,000 and $150,000 annually, depending on experience, the size of the production, and the organization. Salaries can vary widely, with those working for major companies or in large markets earning higher wages. Many opera directors also supplement income through freelance work or consulting on multiple productions.

What are popular job titles related to Opera Director jobs in Wakefield, MA?

For Opera Director jobs in Wakefield, MA, the most frequently searched job titles are:

What cities near Wakefield, MA are hiring for Opera Director jobs?

Cities near Wakefield, MA with the most Opera Director job openings:

Opera Director jobs near you
Infographic showing various Opera Director job openings in Wakefield, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Senior Medical Director, Clinical Development

Beeline Medicines

Boston, MA • On-site

Full-time

PTO

Re-posted 16 days ago

Job description

About Beeline Medicines:
Beeline Medicines is a clinical-stage biotechnology company focused on developing and delivering category-leading precision therapies to transform the lives of people living with autoimmune and inflammatory diseases. With a portfolio of potential best-in-class and first-in-disease therapeutic candidates that directly target key pathways governing dysregulated immunological and inflammatory responses, the Company is developing medicines that have the opportunity to provide durable, life-changing impact. Led by an established executive team and backed by world-class life science investors, each day Beeline Medicines is determined to bring the scientific rigor and operational excellence to get to what matters for patients - realizing a world where people with immune-mediated diseases can live life fully.
Job Summary:
The Senior Medical Director, Clinical Development is a senior physician-scientist who provides strategic medical leadership for one or more clinical programs within the organization's Inflammation & Immunology pipeline. Building on deep therapeutic area expertise and a proven track record in clinical trial execution, this role bridges hands-on clinical program leadership with broader cross-functional and organizational accountability. The Senior Medical Director serves as the primary physician lead for assigned assets, owning the clinical strategy and development plan across multiple phases, while also playing an increasingly prominent role in shaping departmental capabilities, mentoring junior physicians, and contributing to portfolio-level decision-making. This role requires the ability to work with independence and authority in a fast-paced, growth-stage biopharmaceutical environment.
Work Arrangement & Location:
Hybrid - This position follows a hybrid work schedule, requiring a minimum of two (2) days on-site per week - currently designated as Tuesday and Wednesday. Additional on-site days may be required based on business needs, team priorities, or leadership direction.
Essential Duties and Responsibilities:
  • Serve as the physician medical lead for assigned clinical development programs - owning the clinical development strategy, integrated development plan, and medical decision-making for pipeline assets across Phase I through Phase III development, with increasing accountability for program-level outcomes and portfolio contributions.
  • Lead the design, authorship, and review of clinical trial protocols, investigator brochures, informed consent documents, and clinical sections of regulatory submissions (IND, NDA/BLA, global filings) - ensuring scientific rigor, patient safety, and regulatory compliance across all deliverables.
  • Provide comprehensive medical oversight of ongoing clinical trials - including safety monitoring, medical monitoring, SAE assessment, protocol deviation review, and benefit-risk evaluation - in close partnership with Clinical Operations, Pharmacovigilance, and Biostatistics.
  • Lead and actively represent the organization in regulatory agency interactions - including FDA and EMA meetings, briefing document development, and responses to health authority questions - serving as a primary medical spokesperson for assigned programs and contributing to regulatory strategy.
  • Support pharmacovigilance activities during trial conduct - Drive cross-functional clinical program teams as the senior medical lead - providing strategic scientific direction to Clinical Operations, Regulatory Affairs, Translational Medicine, Biostatistics, and Medical Affairs - and ensure integrated, high-quality program execution with clear accountability and pace.
  • Build and maintain relationships with key opinion leaders (KOLs), principal investigators, and academic medical centers to strengthen the organization's clinical network, gather external scientific insights, and support the medical positioning of pipeline assets.
  • Perform other duties and responsibilities as assigned

Qualifications:
  • Education: Advanced clinical degree (MD or DO) required. Board certification or clinical training in rheumatology, nephrology, immunology, or a related specialty strongly preferred. Additional advanced degree (PhD, MPH, or MBA) is a plus.
  • Minimum of 10 years of combined clinical and pharmaceutical/biotech industry experience, with a minimum of 5 years in a clinical development role with increasing levels of responsibility preferred
  • Deep scientific expertise in autoimmune disease - rheumatology preferred.
  • Demonstrated experience as a physician lead on Phase I-III clinical programs, including hands-on protocol development, medical monitoring, and regulatory submission experience
  • Deep clinical and scientific expertise in immunology and inflammation- including command of disease mechanisms, clinical trial landscapes, standard of care evolution, regulatory developments, and emerging therapeutic approaches
  • Proven ability to identify, characterize, and mitigate clinical, operational, and regulatory risks across multi-site, multinational clinical programs
  • Demonstrated ability to serve as the senior medical authority on cross-functional program teams - setting scientific direction, resolving complex medical questions, and building alignment across diverse functional stakeholders
  • Strong track record of leading clinical programs through critical milestones - including first-in-human studies, proof-of-concept readouts, pivotal trial initiation, and regulatory submissions - with a bias for rigor, speed, and quality
  • Effective at delivering data-driven recommendations to senior leadership, adapting communication to drive informed decision-making at the organizational and portfolio level
  • Collaborative and influential leader who builds trust and credibility with clinical investigators, KOLs, and regulatory agencies - leveraging scientific expertise and interpersonal effectiveness to advance the organization's programs and reputation
  • Exceptional scientific and medical communication skills - able to present complex clinical data, safety findings, and development strategies clearly and compellingly to diverse audiences including regulators, investigators, executives, and patient communities
  • Skilled in authoring and reviewing high-quality clinical documents including protocols, investigator brochures, clinical study reports, regulatory briefing documents, and scientific manuscripts

Salary Range:
The expected salary range for this position varies by location and will be communicated based on the country or region in which the selected candidate is hired. Actual pay will be determined based on experience, qualifications, location, and other job-related factors permitted by applicable local law. A discretionary annual bonus and long-term incentive award (e.g., equity) may be available based on individual and Company performance.
Salary Range
$293,000-$379,500 USD
Benefits:
We offer a comprehensive benefits package tailored to the country and region in which you are hired, in compliance with local laws and practices. Benefits may include, but are not limited to:
  • Competitive health and wellness coverage (structure and premiums vary by country)
  • Paid time off, public holidays, and additional leave entitlements in accordance with local requirements
  • Flexible work arrangements / hybrid schedule

Benefits vary by location and are subject to eligibility requirements, local regulations, and plan terms. Specific benefit details applicable to your country or region will be provided during the offer process.
Equal Employment Opportunity:
Beeline Medicines is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, age, protected veteran status, or any other characteristic protected by applicable federal, state, or local law.
Reasonable Accommodation:
If you require a reasonable accommodation to participate in the application or interview process, please contact careers@beelinemedicines.com to request an accommodation. We are committed to providing equal access to all candidates.
PrivacyUpon submission of this form I understand that Beeline Medicines is based in the United States and personal data submitted in the form will be transferred and accessed in the U.S., Information about Beeline Medicines privacy practices can be found at Privacy Policy - Beeline Medicines

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