Bayer HealthCare Pharmaceuticals is one of the world’s leading, innovative companies in the healthcare and medical products industry. Bayer HealthCare combines the global activities of the Animal Health, Consumer Care, Diabetes Care, and Pharmaceuticals divisions. In the United States, Bayer HealthCare Pharmaceuticals comprises the following business units: Women's Healthcare, Diagnostic Imaging, Specialized Therapeutics, Hematology/Cardiology and Oncology. The company's aim is to discover and manufacture products that will improve human health worldwide by diagnosing, preventing and treating diseases. Bayer HealthCare’s pharmaceutical business is dedicated to developing, manufacturing and marketing products that help improve human health, and globally ranks among the top 10 specialty pharmaceutical companies. Outstanding specialty care takes constant innovation and dedication. These core values set by Bayer HealthCare Pharmaceuticals enables us to offer an industry-leading portfolio of products and the support that healthcare providers and their patients require.

During the two-year fellowship, the fellow will be exposed to a variety of areas within the pharmaceutical industry, with a main focus on medical communications (medical and product information) during their first year and medical affairs (Phase IIIb and IV studies) during their second year. The fellow will prepare and maintain a comprehensive, well-balanced, and medically accurate product and disease state database, while interacting with Marketing, Regulatory Affairs, Legal, Product Quality Complaints, and Global Medical Safety. In addition, the fellow will participate in activities involving external thought leaders, advisory boards, and the development and review of marketing pieces as well as interface with Marketing and Sales on a regular basis. In the Medical Affairs Therapy Area, the fellow will participate in the coordinating, managing, and monitoring of Phase IIIb/IV clinical trials and investigator supported studies (ISS), as well as assist in medical education programs, brand plan, and publications.

An optional three-month rotation will also be allocated to the fellow to explore other areas of the pharmaceutical industry, including Health Economics Outcomes and Reimbursements, Field Medical Affairs (MSLs), and Regulatory Affairs. Rotations are flexible and can be tailored to the fellow’s interest.
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The Bimark Center for Medical Education offers a 1-year, post-doctoral fellowship in medical education, an exciting and rapidly growing field within the pharmaceutical industry.  Medical education and communications companies provide a variety of educational and marketing services to manufacturers, making them innovative environments for pharmacists to apply their clinical skills.  Fellows will be an integral part of project teams responsible for the development and management of a variety of programs, including slide kits, journal articles, monographs, live symposia, CD-ROMs, in-service videos, and online continuing education.

An accredited provider of continuing education for physicians, pharmacists, nurses, nurse practitioners, and healthcare executives, the Bimark Center for Medical Education offers an academic, entrepreneurial environment that provides opportunities for long-term professional growth in the pharmaceutical industry. Fellows receive mentoring and hands-on training from every staff member, each of whom is accessible and eager to provide guidance on all aspects of program development and implementation.

Upon completing our program, fellows will be able to:

• Plan and implement continuing education programs and materials that adhere to national accreditation guidelines.
• Collaborate and network with national thought leaders on the creation of educational programs.
• Interact effectively with peers and professional audiences through enhanced written and oral communications.

Bristol-Myers Squibb is dedicated to extend and enhance human life by providing the highest-quality pharmaceutical and related health care products.

Fellowship overview:

• One-year post-doctoral fellowships
• Excellent opportunities to gain experience and exposure in various therapeutic areas, such as cardiovascular/metabolics, neuroscience, oncology, and virology.
• Established fellowship programs in:
• Global Marketing
• Medical Strategy (Cardiovascular, Neuroscience, and Virology)
• Medical Information (Cardiovascular/Metabolics, Medical Information Center (2), and Virology)
• Medical Affairs (Oncology)
• R & D Strategy and Analytics

Fellow roles and responsibilities:

• Become an integral part of functional and matrix teams
• Learn to manage a broad range of responsibilities similar to those managed by current team members.
• Depending on the area, fellows may gain experience with areas/functions including, but not limited to:
• sales training
• drug information
• review of promotional and non-promotional materials
• clinical trial management
• medical writing
• business strategy and planning
• medical marketing
• competitive intelligence
• Strengthen medical expertise, gain in-depth experience, and develop skills needed in the pharmaceutical industry.
• Have the opportunity to develop relationships with various mentors within the company and gain exposure to executive leaders throughout the company at lunch & learn meetings.

Overall, a valuable stepping stone to a career path in the pharmaceutical industry.
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Daiichi Sankyo is located in Parsippany, NJ and is currently offering three unique one-year fellowship positions; two positions available in Medical Affairs and one position available in Market Research.  Tailored to his/her individual interests, each Medical Affairs Fellow and Market Research Fellow will have both a Core Focus and Additional Opportunities.

Core Focus: The Medical Affairs Fellows will enhance Medical Writing skills through creating fair and scientifically balanced Custom Response Letters to unsolicited medical inquiries.  The fellows will assist in developing and maintaining a comprehensive and medically accurate internal product database, as well as strategically monitoring the medical literature to identify data to help leverage the Daiichi Sankyo product line. The fellows will also work with and manage an off-site call center vendor to ensure that product letter databases are up-to-date. The fellows will serve as a scientific resource to a Therapeutic Advisory Group (TAG), and Publication and Advertising Review Committees (PRC) to ensure accuracy and fair-balance as it relates to new Publications, Marketing, and Advertising.  The fellows will develop and deliver presentations as well as support Sales, Managed Care, and Field Medical Affairs.  Periodic travel to attend national conferences and medical meetings is required, as well as to engage in activities pertaining to Key Opinion Leader (KOL) development and training.  Most importantly, the fellows will interact regularly with Marketing, New Product Planning, Regulatory Affairs and Health Outcomes Research as they relate to Medical Affairs’ daily activities and special projects. 

Core Focus: The Daiichi Sankyo/Rutgers New Product Planning Market Research fellowship program offers a unique opportunity for the PharmD graduate to gain valuable industry experience at a pharmaceutical company with a rich research history and a promising future of rapid growth. This 1-year program is designed to provide a comprehensive New Product Market Research overview, allowing hands-on opportunities, active coaching and mentoring, as well as market research and business analytic skill building. Our goal is to help provide fellowship candidates with the tools necessary for highly successful market research careers in the pharmaceutical industry. [Back to top]

Hoffmann-La Roche Inc. (Roche), based in Nutley, N.J., is the U.S. prescription drug unit of the Roche Group, one of the world’s leading research-oriented health care groups with core businesses in pharmaceuticals and diagnostics. The company provides innovative products and services that address prevention, diagnosis and treatment of diseases, thus enhancing people's health and quality of life. The company operates in more than 60 countries, employing more than 68,000 people and selling products in over 150 countries.  Today, Roche invests billions of dollars in original research and development directed towards therapeutic needs in various disease states.

The Fellowship program at Roche is designed to provide a general understanding of the drug development and approval process while allowing fellows to develop specific skills required to function independently and competently in their area of practice.

Novartis is a world leader in pharmaceutical research and development with 91,000 employees in over 140 countries. In the United States alone, Novartis markets over 126 products which helped the company achieve global sales of $32.2 billion.  Novartis Pharmaceuticals, headquartered in East Hanover, New Jersey, creates leading products to treat and prevent disease and enhance lives.  The company’s dedication to research and development is supported by a $4.8 billion annual global R&D investment, which enables it to assemble cutting-edge teams of experts from many fields who collaborate with the world’s renowned research centers. 

The two-year Pharmaceutical Industry Fellowships at Novartis are designed to identify practice opportunities for pharmacists within the pharmaceutical industry.  Fellowship opportunities during the initial year of the program are typically offered in the department listed below with the opportunity to rotate to a different department during the final year of the program:

• Translational Medicine (Phase I)
• Clinical Development (Phase II to III)
• Medical Affairs (Phase IV)
• Drug Regulatory Affairs
• Marketing
• Project Management
• Modeling & Simulation
• Integrated Medical Safety

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Ortho-McNeil Janssen Scientific Affairs, LLC supports primary care, neurology, and psychiatry products.  This Medical Communications fellowship is a one-year program, which allows the fellow to develop and expand upon various skill sets in the medical communications division including medical writing, presentation, and communication skills.  This unique experience is further enhanced through the option of rotating for up to three months in various departments including Marketing, Regulatory Affairs, and Business Intelligence, etc.  The fellow will be involved in evaluating medical literature, creating and updating standard responses, developing formulary dossiers, conducting Sales Training, responding to inquiries from health care practitioners and internal customers regarding marketed products, and working closely with several departments on various projects relevant to the medical communications sector.  A wide range of opportunities exists for the fellow to attend national conferences and scientific meetings, present posters, precept Pharm.D. students, and potentially participate in product launches.  Fellows are given the opportunity to be an integral part of the medical communications team while also gaining teaching experience through various programs at Rutgers University.

The Marketing Research fellowship program at Pricara, a Unit of Ortho-McNeil, Inc. is designed to allow the fellow to work closely in a wide variety of marketing research areas including product positioning research, professional and consumer advertising research, and strategy development. The fellow will have the opportunity to gain exposure to the forecasting/business planning process as well. In addition to the Ortho-McNeil, Inc. responsibilities, the fellow will also participate in various activities through Rutgers University.

The Fellowship program, jointly offered by McNeil Consumer Healthcare and Johnson & Johnson Healthcare Products, will provide training and exposure to various aspects of the consumer healthcare industry while enabling the Fellow to gain an overview of drug development and pharmaceutical industry experience. The Fellowship is composed of primary rotations in Clinical Research/Medical Affairs and Regulatory Affairs, as well as opportunities to rotate externally through prescription companies. The Fellowship will encourage participation on cross-functional teams in order to learn from internal professionals in various areas of the company, including research and development, marketing, sales, business development, public relations, drug safety and legal. Opportunities are also available for collaboration with external experts and stakeholders. The program is designed to provide the Fellow with scientific, medical and regulatory skills that serve as a solid foundation for a successful career within the pharmaceutical industry. Fellows may participate in special projects of interest and have opportunities to attend training seminars and workshops to build professional skills as well as written and oral presentation skills. Fellows may be eligible to attend professional society meetings where they may present posters, participate in scientific sessions and network with colleagues in pharmacy practice or the pharmaceutical industry.

Regulatory Affairs

Regulatory Affairs proactively drives the business forward and fosters continued innovation by working to develop new products and claims, support current marketed products, and maintain a high level of compliance, while building strong working relationships with internal colleagues, FDA, other Regulatory Authorities and other external stakeholders. Regulatory Affairs preceptors are considered subject matter experts within their therapeutic areas. The Fellow can expect their preceptor to provide assignments which are challenging and which provide the Fellow with the opportunity to broaden their professional experience while allowing them to enhance their academic and leadership potential. The Fellow will have frequent interactions with colleagues in marketing, legal, research and development and project management and will be provided the opportunity to participate in project teams which oversee the development and launch of new products. The Fellow will have the opportunity to network with other professionals within the Company in order to facilitate an overall understanding of the industry. In an effort to provide a well-rounded experience, the Fellow may also have the opportunity to rotate to various therapeutic areas within regulatory affairs, including the pharmaceutical research and development sector of the company.

The successful candidate within Regulatory Affairs will develop working knowledge and skills through project experiences which can include the following:

• support for new product development (ex., Rx-to-OTC switch; IND, NDA, etc.)
• interaction with FDA and other Regulatory Authorities and global affiliates;
• marketed product support (e.g. claims and advertising, etc.)
• product strategy –including proactive shaping of external environment issues related to our products;
• analysis of external environment issues and interactions with stakeholders
• developing written assessments, briefings, presentations and responses
• development, review and approval of product labeling

Medical Affairs/Clinical Development

Clinical Research is responsible for the development of new OTC products, including Rx to OTC Switches, new chemical entities, dosage forms and indications, medical devices, and development of new claims for consumer care products. Responsibilities also include developing detailed program/study management plans to implement and conduct clinical trials. Clinical research activities will allow the Fellow to develop knowledge regarding various research methodologies, Good Clinical Practice (GCP), requirements for an Investigational New Drug Application (IND), New Drug Application (NDA), and 510(K)s for medical devices as well as other regulatory guidelines for conducting clinical research. There will also be opportunities to work in specific therapeutic areas, such as oral care, for both prescription products and OTC products.

Professionals in Medical Affairs maintain expertise to support currently marketed products. Medical Affairs drives business growth through innovation. Fellows will develop skills in new product development, claims substantiation, the design and conduct of clinical trials and the overall assessment and application of science as a competitive advantage as it relates to Company products.

The Fellow in the Clinical Research rotation may participate directly in the design or conduct of a clinical trial including the following activities:

• Protocol design and execution of Phase I-IV studies
• Investigator and site selection
• Study site initiation, monitoring, and closing
• Writing study reports, investigator brochures, case report forms, and other trial related materials
• Adverse event reporting
• Study staff training and site management
• Data management and analysis

Sanofi-aventis will be offering both 1 and 2-year fellowships.

Medical Information
The U.S. Medical Information Services (MIS) department at sanofi-aventis provides medical and drug information on sanofi-aventis products and therapeutic areas to healthcare professionals, consumers, and internal associates.  Medical information specialists offer expertise in the cardiovascular, CNS/rheumatology, metabolism, oncology/urology, and respiratory/dermatology. 

Upon completion of this one-year Medical Information Fellowship, the Fellow will have accomplished the following objectives:

• Provide efficient and unbiased medical information on sanofi-aventis products
• Develop strong literature searching and evaluation skills
• Optimize written and verbal communication skills
• Excel in teamwork and leadership skills
• Complete a fellowship research project to be presented at a national conference
• Enhance professional growth in both the pharmaceutical industry and academia

Medical Education & Scientific Publications

Sanofi-aventis is offering a one-year Post-Doctoral Fellowship in U.S. Medical Education & Scientific Publications. The Medical Education and Publication department establishes an ongoing process of education for physicians and health care professionals that foster optimal medical knowledge to enhance patient care.   The Fellow will be involved in planning and managing medical education and publications throughout the year for various professional associations, major medical meetings, and reputed journals.  During the year the Fellow will attend medical meetings and have the opportunity to interact with national thought leaders. The Fellow will also have the opportunity to pursue two rotations in other disciplines of interest. Upon completion of this one-year fellowship, the Fellow will:

• Develop strategic publication planning expertise
• Understand the process of medical education and publications within the   pharmaceutical industry
• Enhance project management and strategic planning skills
• Attend national and regional meetings to serve as a liaison with medical experts and medical education companies
• Participate in the Medical/Regulatory/Legal approval process of educational grants
• Manage publications, abstracts, live educational symposium, and web based enduring material
• Gain experience and knowledge of the pharmaceutical industry and academia
• Develop budget management skills
• Develop and enhance teamwork and leadership skills

US Managed Markets

Sanofi-aventis is offering a two-year post-doctoral US Managed Markets (2 positions). The USMM team at sanofi-aventis increases patient care by demonstrating and communicating the value of our pharmaceutical products to key stakeholders. The highly skilled USMM team composed of pharmaceutical industry professionals understands the healthcare business climate, its needs, and the ultimate impact on key stakeholders in the healthcare marketplace.

As a USMM Fellow, significant experience will be gained in USMM that may include Employer and Quality Association Account Management, Managed Markets Operations, Managed Markets Marketing, Trade, National and Regional Account Management, Institutional and Federal Account Management. To gain in-depth knowledge and experience of the pharmaceutical industry, fellows may elect to rotate through Brand Marketing and other commercial and medical departments.

During this two-year US Managed Markets fellowship, the fellows will:

• Develop an in-depth understanding of the healthcare marketplace and the current trends in key segments including managed care, employers, senior care, hospitals, and others
• Identify and assess the needs of key stakeholders and entities relevant to U.S. Managed Markets including health maintenance organizations, pharmacy benefit managers, employers, group purchasing organizations, government, trade, long-term care, professional associations, quality organizations, and integrated health systems
• Assist in the development of strategies and tactics to ensure portfolio objectives are being achieved
• Ensure new and ongoing initiatives and programs are successfully implemented and executed
• Develop leadership skills that emphasize creativity, performance, audacity, courage, respect, and solidarity
• Explore potential employment opportunities within the pharmaceutical industry by completing a variety of rotations within U.S. Managed Markets and other key business divisions

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At Schering-Plough, we aspire to earn the trust of doctors, patients, customers, and other stakeholders by providing a steady flow of innovative, science-based medicines and services that improve the health and well-being of people around the world.

Purpose of the Program:
This distinctive two-year program provides practice opportunities within Schering-Plough that will enable individuals with a Doctor of Pharmacy degree to gain in-depth exposure in a variety of areas within the organization. Additionally, fellows will have the opportunity to enhance their academic and traditional clinical pharmacy experience in conjunction with Rutgers University. Overall, the program is a challenging post-doctoral experience that will provide the individual with the training and the knowledge to pursue a career within the pharmaceutical industry.

Objectives of the Program:

• To provide fellows with in-depth experience in the fields of Clinical Research, Clinical Pharmacology, Regulatory Affairs or Global Medical Affairs/Global Medical Information.
• To provide individuals with the opportunity to expand their knowledge of pharmacy by participation in academic, clinical and industry initiatives.
• To provide exposure to potential employment opportunities within the pharmaceutical industry.

The Schering-Plough Component:
The two-year post doctoral fellowship is designed to provide a general understanding of the drug development process while allowing an in-depth understanding of specific departments within Schering-Plough, including the Schering-Plough Research Institute (SPRI). While concentrating in one particular area of the company, individuals have numerous opportunities to interface with many different departments within the organization.

Available core rotations include:

• Global Clinical Development (Clinical Research)
• Early Clinical Research and Experimental Medicine (Clinical Pharmacology)
• Global Regulatory Affairs
• Global Medical Affairs/Global Medical Information

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