1,000+ matching jobs for “Business Development Director”

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IQVIA Holdings

Associate Director, Medical Writing

Durham, North Carolina, United States

… in global teams and interaction with regulatory agencies in multiple regions This role reports to the Director of Medical Writing Senior Medical Writer(s) and Medical Writer(s) will report to this role Main …

Added Oct 15, 2026

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Arrow Electronics

Sales Director - North China

CN-Shanghai, China (Raffles City The Bund) +1 location

Full time
Regular

… towards the achievement of maximum sales, profitability and growth. As the leader for the Arrow, the Director, Sales creates a vision for their team and ensures their effectiveness by organizing analytics, improving …

Added Oct 27, 2026

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Adobe

Director Product Manager

San Jose, California, United States

Full time
Regular

Pay posted by employer$172,400–$334,500 per year

… an overall product roadmap. Measure and assess the efficacy of the product roadmap for customer delight and business success · Introduce capabilities in the product and partner with GTM teams to take an early-stage product …

Added Oct 27, 2026

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Vertex Pharmaceuticals

Epidemiology Forecasting, Associate Director

Boston, Massachusetts, United States 2 postings

Full time
Regular

Pay posted by employer$172,000–$258,000

… aimed at transforming the lives of people with serious diseases, their families, and society. The Associate Director role is within HEOR’s Epidemiology Center of Excellence (CoE), a specialized team that develops patient …

Added Nov 7, 2026

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Johnson & Johnson

Director, Web Product Management

New Brunswick, New Jersey, United States +1 location

Full time
Regular

Pay posted by employer$164,000–$282,900

We are searching for the best talent to join the Corporate Brand Equity team as the Director, Web Product Management. This position has a primary location of New Brunswick, NJ but consideration will …

Added Oct 15, 2026

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GE HealthCare Technologies

Senior Director, Software Engineering

IND19-01-Bengaluru-EPIP 122 (Phase II)

Summary Heartbeat is GE HealthCare's proprietary business system, our standard way of working together to deliver on commitments to people, patients, and customers. …

Added Oct 28, 2026

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Cisco Systems

Director, Product Management

San Francisco, California, United States +3 locations

Pay posted by employer$233,900–$330,400

… You will influence senior leadership and help steer the direction of our incubation portfolio. As the Director of Product Management, you will lead the strategy for emerging technologies including quantum networking …

Added Oct 27, 2026

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Venture Global

Director, Operations - Power Island

Plaquemines Parish, LA

Full time
Regular

of Director, Operations – Power Island Summary The Director, Operations - Power Island is a key leadership position …

Added Nov 3, 2026

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Centene

Behavioral Health Medical Director

Remote-CA

Full time
Regular

Pay posted by employer$215,000–$408,500 per year

Position Purpose: Assist the Chief Medical Director to direct and coordinate the medical management, quality improvement and credentialing functions for the …

Added Oct 29, 2026

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Centene

Remote Medical Director, Appeals

Remote-MO +9 locations

Full time
Regular

Pay posted by employer$215,000–$408,500 per year

Position Purpose: Assist the Chief Medical Director to direct and coordinate the medical management, quality improvement and credentialing functions for the …

Added Oct 27, 2026

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Centene

Remote Medical Director, Pharmacy

Remote-FL +10 locations

Full time
Regular

Pay posted by employer$236,500–$449,300 per year

Position Purpose: Assist the Chief Medical Director to direct and coordinate the medical management, quality improvement and credentialing functions for the …

Added Oct 27, 2026

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Centene

Remote Medical Director, Appeals

Remote-MO +5 locations

Full time
Regular

Pay posted by employer$236,500–$449,300 per year

Position Purpose: Assist the Chief Medical Director to direct and coordinate the medical management, quality improvement and credentialing functions for the …

Added Oct 27, 2026

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Capital One Financial

Director, Technical Program Management

McLean, Virginia, United States +3 locations

As a Director of Technical Program Management (TPM), we’re looking for someone that can help us lead programs that …

Added Oct 27, 2026

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Thermo Fisher Scientific

Associate Director, Pharmacovigilance- FSP

Chapel Hill, North Carolina, United States

Join Us as a Associate Director, PV At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global …

Added Oct 30, 2026

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Hartford Insurance Group

IND Director, Software Engineering

India GCC-Puppalaguda Village

Regular

Director of Software Engineering Location: Hyderabad, India Employment Type: Full-Time Experience Level: 14 -16 …

Added Nov 3, 2026

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Thermo Fisher Scientific

Medical Director/Sr Medical Director - Neurology(Remote U.S)

Remote, North Carolina, USA

Join Us as a Medical Director – Make an Impact at the Forefront of Innovation At Thermo Fisher Scientific, you’ll discover meaningful …

Added Oct 16, 2026

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TD Synnex

Business Manager- Palo Alto

Bengaluru, Karnataka, India

Full time
Regular

… for managing the profit and loss of all applicable vendors including current and new vendors Work with Business Unit Director, Vendor Business Executive, Vendor Operations Executive and Client Executives to analyse and …

Added Oct 27, 2026

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Merck (MSD)

Executive Director, PDMB Outsourcing

USA - Pennsylvania - West Point +3 locations

Pay posted by employer$255,800–$402,700

The department of Pharmacokinetics, Dynamics, Metabolism and Bioanalytics (PDMB) is seeking an Executive Director to lead the Outsourcing team within the Translational Sciences and Outsourcing (TSO) organization. The …

Added Oct 16, 2026

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Coca-Cola

Director, Marketing Capability & Transformation

Tokyo, Tokyo, Japan

Summary: Director, Marketing Capability & Transformation Job Description Summary In Japan, one of our most dynamic markets, …

Added Oct 27, 2026

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The Home Depot

Director, Federal Tax Planning

STORE SUPPORT CENTER, ATLANTA - 9090 +1 location

In person
Full time
Regular

… appeals, controversy, and related tax matters as needed to meet the goals of the Tax Department. Lead the development, evaluation, and execution of tax strategies aligned with Company priorities, business operations, …

Added Oct 16, 2026

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IQVIA Holdings

Associate Director, Medical Writing

Durham, North Carolina, United States

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Experience · employer excerpt

A minimum of 8 years medical writing experience within the biopharmaceutical

About this opportunity

Original employer description

The Associate Director is a key leadership position responsible for determining and driving the medical writing strategy for one or more therapeutic areas within Clinical Development.

As a strategic partner to senior clinical leadership, the incumbent is accountable for the efficient preparation of high quality, strategically aligned medical writing deliverables that support the clinical development, clinical safety and regulatory requirements of a clinical program. He or she is also responsible for the messaging strategy across a program of work, for the provision of strategic input into the development of clinical development plans and submission plans, and for analysing proposed plans, programs, individual studies and related documents for their ability to deliver the information required by the target audience (ie, regulatory authority) in a compelling fashion with accuracy and consistency

This role has global responsibilities with potential for global reports, participation in global teams and interaction with regulatory agencies in multiple regions

This role reports to the Director of Medical Writing
Senior Medical Writer(s) and Medical Writer(s) will report to this role

Main Responsibilities and Accountabilities

Leads the Medical Writing contributions to assigned therapeutic area(s). Key accountabilities:
Maintain a collaborative and strategic partnership with Global Therapeutic Area Leads, Global Clinical Program Directors and Clinial Safety Physicians to ensure understanding of Clinical Development strategy for the therapeutic area and the nature of medical writing services required to deliver on company objectives
Critiques ability of product strategy (eg, submission plans) to deliver on business objectives or meet regulatory needs, and identify where new or alternative arguments are needed.
Leads cross-functional teams to develop a messaging strategy across a program of work (eg, building a clinical submission)
The efficient preparation of medical writing deliverables for assigned clinical program(s) according to budget and timelines
Forecasting, budgeting, resource planning and resource allocation.
Managing (Senior) Medical Writer(s) within therapeutic area(s). Coach, train and mentor staff, thereby contributing to successful clinical development, product registration in key regions and commercialization of new compounds, including important lifecycle management work

Drives and develops the messaging strategy within the therapeutic area to ensure effective communication underpins successful clinical development

Responsible for aligning, coordinating and building consistent information and messages across all individual documents within a clinical program, starting with intial strategic plans, continuing through study level documents to final program level deliverables (ie, regulatory submission or publication of key journal articles for a publication plan).

Interfaces with Global Therapeutic Area Heads, Global Clinical Program Directors and Clinial Safety Physicians to ensure that the communication needs for clinical data are considered early in the development program to enable consistency of data presentation and messaging throughout the clinical development process.
Analyses proposed plans, programs, individual studies and related documents for their ability to deliver the information required by the target audience (ie, regulatory authority) in a compelling fashion with accuracy and consistency.
Understands where all intended messages will be located across individual documents within a clinical program, and ensures alignment of messages across documents.
Understands issues affecting the design of clinical development strategy, and understands how study design, data capture and statistical analysis plan design will affect downstream documents.
Responsible for ensuring that statements included in the deliverables are accurate and supported by appropriate data
Accountable for medical writing deliverable quality and ensures adherence to departmental procedures / practices, and industry / international standards.
Responsible for the development, implementation and communication of Best Practices, SOPs, templates, work instructions, style guides and content guides to ensure efficient preparation of high quality medical writing deliverables.

Cultivates an understanding of modern medical writing processes and solutions through survey of relevant literature, attendance at meetings and use of international external networks.
Responsible for continual improvement of in-house medical writing.
Provides expert medical writing support to other CR&D and CSL groups where required
In collaboration with Director, Medical Writing and Disclosure, ensures appropriate medical writing support for the clinical programs including forecasting, budgeting, resource planning and resource allocation
Responsible for building and maintaining collaborative relationships with medical writing partner(s) (CRO, vendor, alliance partner, etc) to ensure an effective, efficient, productive and professional working relationship. Participates in vendor governance.
Participant in bid defense, contract development, work alignment and / or operation meetings.
Post-graduate qualifications (PhD or MD preferred)

Experience

A minimum of 8 years medical writing experience within the biopharmaceutical

industry or a contract research organization.

A minimum of 3 years in a supervisory role

A comprehensive understanding of the clinical development process, including the

documents that are required at each stage.

A comprehensive understanding of medical writing processes, standards and issues.

Demonstrated track record in cross-functional, multicultural and international clinical trial teams
Excellent verbal, written and presentation skills.
Mastery of the English language, with a comprehensive understanding of English grammar and punctuation
Prior experience with submissions in Common Technical Document (CTD) format.
Knowledge of eTechnology related to regulatory submission activities (eCTD, EDMS, Life Cycle Management
Expert MS Office skills with a special focus on word processing, tables, spreadsheets, presentations, graphics and template

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

As the COVID-19 virus continues to evolve, IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status

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