Working for the drug industry
Pharmaceutical medicine offers a challenging and rewarding medical career, says Stephen Jones
Pharmaceutical medicine became a recognised specialty in 2002 It provides the opportunity to advance the therapeutic armamentarium
available to clinicians, and the satisfaction that you are helping patients worldwide. After working in the NHS for five years
I switched to the drug industry and found my knowledge and skills transferable.
How does the drug industry work?
Activities in the industry differ depending on the stage in a drug’s development. Before a drug can be marketed the industry
has to show appropriate manufacturing standards and establish the drug’s risk-benefit profile (using information from toxicology
and clinical trials). The prospectively collected safety and efficacy data are put before the regulatory authorities, who
evaluate whether the efficacy shown outweighs the risk or potential risk. If the balance is favourable the drug may be approved
for marketing. If it is approved, postmarketing activities include marketing for any indications agreed with the local regulatory
authority and continuous safety monitoring. Additional (phase IV) clinical trials may be undertaken. Most drugs don’t make
it to the market, so their research and development costs are recouped by the few that do.
What roles are available to doctors?
The industry adopts a multidisciplinary approach and the roles available to the pharmaceutical doctor are varied. Premarketing
research roles (clinical pharmacology and clinical development) entail working on phase I-III clinical trials; postmarketing
roles (medical affairs or marketing) ensure accuracy of promotional material and input into phase IV clinical studies, and
may involve training medical representatives. Other roles include drug safety officer (pharmacovigilance) to monitor drug
safety and changes to a drug’s risk-benefit profile. Regulatory roles are within the regulatory authorities (for example,
the Medicines and Healthcare Products Regulatory Agency in the United Kingdom) or within companies, to ensure regulatory requirements
are met. Health outcomes-economics is an expanding area and evaluates the cost effectiveness of drugs, which helps obtain
recommendation and reimbursement from the National Institute for Health and Clinical Excellence.
Box 1: Examples of roles and activities within companies
- Clinical pharmacology—Early phase development (phase I and IIa)
- Clinical development—Later phase trials (phase IIb and III) to obtain approval to market drugs
- Medical affairs and medical marketing—Dealing with drugs on the market, reviewing promotional material, and inputting into
post-marketing clinical trials (phase IV)
- Drug safety (pharmacovigilance)—Evaluating overall safety and risk; compiling reports for the company and regulatory authorities
- Regulatory affairs—Ensuring company meets regulatory requirements
- Health outcomes—Dealing with quality of life and economic evaluations (pharmacoeconomics)
Working environment
Responsibilities depend on the size and culture of the organisation, with greater subspecialisation in larger companies. The
“big pharma” environment entails integration with many teams, and daily meetings are common. Working closely with experienced
colleagues you will rapidly develop an understanding of the industry. Small companies provide more role diversity and an entrepreneurial
environment, with freedom to progress your ideas. Clinical research organisations undertake outsourced work (phase I or international
phase II and III trials) and give the pharmaceutical doctor hands-on experience of running clinical studies.
What is a typical working day like?
There’s probably no such thing as a typical day in the drug industry. Depending on your role, your day will probably start
between 8 and 9 am and finish at about 6 to 7 pm. You may have late calls with your international offices, which can usually
be taken at home. My day often entails writing and responding to emails in the morning, possibly two or three meetings (some
multidisciplinary), researching the internet, writing or reviewing various company reports or protocols, and putting together
plans and strategies to achieve the company’s goals.
What is the workload like?
Work intensity fluctuates, but don’t think that pharmaceutical medicine is an easy option. You often have deadlines to meet
and have to balance the wants and needs of other departments with yours. International travel is quite common, but the industry
provides a comfortable way of seeing the world. It can be a stressful environment—something you are used to as a medic.
Is it ethical, and how transparent is it?
It can be frustrating to read the negative opinions in the press, but most pharmaceutical doctors share the view that the
drug industry does research to an impeccable standard and is ethical, and although questions may surround the cost and methods
of marketing, some form of proactive dissemination of product information is necessary to ensure the latest risk-benefit profile
is recognised by clinicians. As a pharmaceutical doctor you won’t provide the sandwiches at lunchtime meetings (or pens),
but you may be responsible for writing or overseeing promotional material and ensuring this complies with local guidelines
(for example, the code of practice of the Association of the British Pharmaceutical Industry).
The industry is becoming more open with information available on the internet. Clinical trials are now listed (for example,
www.clinicaltrials.gov), and companies may be asked to present at open forums. I presented clinical data to a Food and Drug Administration advisory
committee in the United States. The meeting was broadcast internationally and open to the press, public, and clinicians. The
data gathered had to stand up to the highest scrutiny before marketing approval was granted.
The drug industry operates in a competitive environment and therefore some degree of confidentiality has to be maintained.
Safety data, however, should always be transparent.
What about job security?
The industry can’t offer the security provided by the National Health Service because of greater exposure to political, economic,
and technical changes. Career security is good within the industry, however, with considerable flexibility, no limits on available
positions, and its worldwide expansion. The industry always needs medics and once you have gained some pharmaceutical experience,
that experience can be valuable to another company.
With regard to the recent economic downturn, the drug industry tends to be relatively resilient to recession. Some smaller
companies are finding difficulty obtaining funding, with initial public offerings becoming more difficult and the venture
capitalists streamlining their investment portfolios. It is worth inquiring (from your recruitment consultant) about the level
of funding and projected spending, certainly for small companies. Larger companies reduce their workforce from time to time.
Medics are not immune, but their roles are more secure than most. When redundancy does occur, companies typically look after
their employees well. They can be generous with the severance package (with up to £30 000 being tax free), and often employees
find alternative employment before completing their notice period. With the various roles available to pharmaceutical doctors
and the pivotal part they play in the industry, jobs are usually available for them.
What about job satisfaction?
The job reward comes from completing positive clinical trials, gaining regulatory approval to market your drug, ensuring your
drug’s safety, developing a successful risk management plan, or even establishing the product’s pharmacokinetic profile to
take it to the next stage of development. Treating patient populations worldwide (rather than individuals) provides the satisfaction
that you are making a difference. It does involve a different mindset though. The benefits of working in an environment where
tasks are performed quickly, things tend to run efficiently, and you focus on the job you are good at make life easier and
more satisfying. The industry takes evidence based medicine to the highest level. The concept of medicine being a non-exact
science does not sit well here.
What about training?
I gained my certificate of completion of training last year, and training was provided mainly on the job with some external
courses. Once you are qualified I would recommend registering on the pharmaceutical medicine specialty training scheme (previously
known as higher medical training). The Faculty of Pharmaceutical Medicine’s website covers this in detail (see further information).
Most companies encourage training as it is in their best interest to make sure you have access to all the latest information.
Doctors registered with the General Medical Council can sit the diploma in pharmaceutical medicine after working in the drug
industry for two years. Be warned, this is by no means an easy exam and you will need to prepare as for any other postgraduate
exam.
What about pay?
Your salary will probably be slightly higher than your NHS pay. Benefits such as bonus, car allowance, payment of professional
subscriptions, laptop, and mobile phone improve the total remuneration package. In addition, the company may issue share options,
which can be lucrative if your company does well.
The biggest hurdle is getting into the industry. Once you have pharmaceutical experience under your belt your value can go
up quite rapidly.
Competing interests: SJ is managing director of Synapse Medical Resourcing, which specialises in medical recruitment for the
drug industry; chief executive officer of Althean Pharma; and a consultant to various drug companies. He previously worked
as medical director and head of clinical development for Elan Pharmaceuticals and medical director to SLA Pharma.
This article was first published in BMJ Careers (2008 Sep 3 http://careers.bmj.com/careers/advice/view-article.html?id=3055).
Stephen Jones managing director and consultant to the pharmaceutical industry Synapse Medical Resourcing, London
sjones@synapsemr.com
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