Associate Director Jobs in Massachusetts

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48 Massachusetts Associate Director jobs found on Monster.

Jobs 1 to 20 of 48
Sanofi-Aventis Framingham, MA
Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to...
Sanofi-Aventis Framingham, MA
Description The CMC Dossier Development and Coordination (CDDC) department within the Sanofi R&D Scientific Core Platforms (SCP) organization has the broadly defined roles and responsibilities for the development, coordination and delivery of high-quality CMC dossiers in a timely manner for all small and large molecule based pharmaceutical and biopharmaceutical products from First in Human clinic...
Sanofi-Aventis Framingham, MA
Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to...
Biogen Idec Inc Cambridge, MA
As a member of the Biogen Idec’s protein pharmaceutical development team, the candidate will be responsible for building and managing a small scale drug product fill finish process development suite. The development fill finish suite is intended to support aseptic fill-finish process development activities for biological pipeline candidates, including the design, execution, and analysis of experim...
Merck & Co. RTP, MA
Description Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and te...
This position is for an experienced, motivated individual to serve as strategic IT liaison to the U.S. Commercial Effectiveness and Operations (CE&O) organization, focused on building strong partnerships and delivering operational, strategic and meaningful IT solutions. This role includes driving a 3 year roadmap in how Biogen Idec can, in partnership with the business, drive technical innovation...
Location: Framingham, MA Job Category: General Services Jobs Requisition Number: 70037550-4146 Associate Director, Biologics CMC Dossier Development and Coordination-70037550-4146 Description The CMC Dossier Development and Coordination (CDDC) department within the Sanofi R&D Scientific Core Platforms (SCP) organization has the broadly defined roles and responsibilities for the development, c...
Location: Cambridge, MA Job Category: Regulatory Affairs Jobs Requisition Number: 33840 Associate Director, Regulatory Affairs, Biosurgery-33840 Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global ...
sanofi-aventis U.S. LLC. Framingham, MA, 01702
Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to making a pos...
">Summary of Responsibilities In this role the Associate Director is accountable for strategic and tactical execution of the Sales Incentive Compensation (IC) Plans for all Sunovion Field-based personnel. This will include creating incentive compensation plan structures, providing goals and interim tracking reports, as well as calculating results and ensuring data integrity with respect to sales c...
Location: Framingham, MA Job Category: Quality Jobs Requisition Number: 70070953-37853 Associate Director Quality-70070953-37853 Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient communit...
sanofi-aventis U.S. LLC. Bridgewater, MA
Global Market Research Associate Director – Rheumatology Department/Group PCS – IMMUNO-INFLAMMATION GSU Reporting To Global Commercial Team Leader or Sr. Director Global Professional Leader – IL6 Main missions The Global Market Research Associate Director will work and collaborate very closely with the Head of IL 6 Strategic Unit Associate Director and with Regeneron global market research cou...
Shire Pharmaceuticals Inc Lexington, MA, 02421
Primary Duties: The Associate Director, Epidemiology is a strategic and scientific role that involves developing, coordinating, and executing cutting-edge, effective, and impactful epidemiology research for product support at a global level, from early development through life cycle management. The Associate Director, Epidemiology provides essential specialist guidance and direction to projec...
Shire Pharmaceuticals Inc Lexington, MA, 02421
Primary Duties: Under the direction of the Pharmaceutical Analysis (PA) Director, the Associate Director is responsible for supporting global product development within the Pharmaceutical Sciences (PS) department. This position is for a high level, experienced analytical professional to serve as an analytical subject matter expert and point of contact for Shire’s product development group (for sy...
Shire Pharmaceuticals Inc Lexington, MA, 02421
Primary Duties Under the direction of the Director, QMS Standards, Training & Risk Management, this position is responsible for executing activities related to procedural document development, training development and deployment, and facilitation and implementation of operational excellence process improvement activities within R&D QA & Compliance and R&D as a whole. This includes but is not limi...
Shire Pharmaceuticals Inc Lexington, MA, 02421
PRIMARY ROLES: The Regulatory Technologies and Information Management Lead will further the vision for Global Regulatory Affairs (GRA) in alignment with the One Shire business model to establish and support the new/existing systems and Regulatory information management needs within GRA. This individual will collaborate with all functions within GRA and R&D IT to contribute to the direction and im...
Shire Pharmaceuticals Inc Lexington, MA, 02421
Primary Duties: •Responsible for the effective uninterrupted support of manufacturing activities for the designated Shire manufacturing site •Represents Facilities and Engineering Organization at the Site Leadership Team (SLT) •Responsible for efficient and productive operations of the Facilities group assigned to the Plant •Facilitates execution and ensures effectiveness of the Preventive and...
Merck & Co. RTP, MA
Description Merck is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and te...
Heartware International, Inc. Framingham, MA, 01702
Position Summary: Interpret regulatory requirements and guidelines and provides regulatory guidance and support throughout the product lifecycle. Basic knowledge of domestic and international regulatory markets, due diligence process and regulatory intelligence. Confers with management personnel to assist in the development and maintenance of global regulatory strategies. Define and compile relev...
Shire Pharmaceuticals Inc Lexington, MA, 02421
Primary Role: •The Compliance Systems IT Services Manager is accountable for the technical delivery and support of all technology solutions that enable compliance for Quality Assurance (QMS), Supply Chain (Artwork Management), and Facilities (Calibration Management) functions. •The Services Manager is responsible for managing all IT aspects of application delivery, maintenance, and integration a...

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Engineering Career Tools

Clinical Research Associate Director

Salaries

$66,000.00 - $181,250.00
Typical Salary for Clinical Research Associate Director in Massachusetts
(75 Respondents)
Source: Monster.com Careerbenchmarking Tool

Education / Training

Master's
34%
Doctorate
32.1%
Bachelor's
26.4%
Associates
3.8%
(53 Respondents)
Source: Monster.com Careerbenchmarking Tool

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