In Summary - Clinical Trials Scientist
Clinical Trials Scientists typically work in the following Career Sectors:
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The Work - Clinical Trials Scientist
Clinical trials scientists work in the pharmaceutical industry. They carry out clinical trials or tests on the effectiveness and safety of new drugs and medicines. Trials take place over a lengthy period - sometimes it can take years before results are clear.
Trials scientists decide on the size of the study, the methods to be used in collecting and analysing data, and how to report and publicise eventual findings. They also liaise and co-ordinate with research staff, general practitioners, hospital doctors and other medical professionals.
In addition to laboratory based research, trials frequently involve the assistance of willing, healthy volunteers and patients. This helps to confirm the results of initial laboratory tests carried out on animals. Trials scientists are responsible for ensuring that guidelines governing the use of humans or animals in clinical trials are strictly observed.
Statistical methods are used to analyse and evaluate the large amount of data generated by trials. Computers are also used to support research and analysis. They also have the responsibility to interpret results and write technical reports.
Most commonly reported Work Tasks
- Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
- Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
- Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
- Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
- Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
- Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
- Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions.
- Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
- Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
- Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks.
Most commonly reported Work Activities
- Getting Information Observing, receiving, and otherwise obtaining information from all relevant sources.
- Establishing and Maintaining Interpersonal Relationships Developing constructive and cooperative working relationships with others, and maintaining them over time.
- Making Decisions and Solving Problems Analyzing information and evaluating results to choose the best solution and solve problems.
- Organizing, Planning, and Prioritizing Work Developing specific goals and plans to prioritize, organize, and accomplish your work.
- Updating and Using Relevant Knowledge Keeping up-to-date technically and applying new knowledge to your job.
- Communicating with Supervisors, Peers, or Subordinates Providing information to supervisors, co-workers, and subordinates by telephone, in written form, e-mail, or in person.
- Documenting/Recording Information Entering, transcribing, recording, storing, or maintaining information in written or electronic/magnetic form.
- Processing Information Compiling, coding, categorizing, calculating, tabulating, auditing, or verifying information or data.
- Scheduling Work and Activities Scheduling events, programs, and activities, as well as the work of others.
- Interacting With Computers Using computers and computer systems (including hardware and software) to program, write software, set up functions, enter data, or process information.
Interests - Clinical Trials Scientist
This occupation is typically suited for people with the following Career Interests:
Enterprising people like situations that involve using resources for personal or corporate economic gain. Such people may have an opportunistic frame of mind, and are drawn to commerce, trade and making deals. Some pursue sales and marketing occupations. Many will eventually end up owning their own business, or in management roles in larger organisations. They tend to be very goal-oriented and work best when focused on a target. Some have an entrepreneurial inclination.
The Investigative person will usually find a particular area of science to be of interest. They are inclined toward intellectual and analytical activities and enjoy observation and theory. They may prefer thought to action, and enjoy the challenge of solving problems with sophiscticated technology. These types prefer mentally stimulating environments and often pay close attention to developments in their chosen field.
Administrative people are interested in work that offers security and a sense of being part of a larger process. They may be at their most productive under supervisors who give clear guidelines and while performing routine tasks in a methodical and reliable way.
They tend to enjoy clerical and most forms of office work, where they perform essential administrative duties. They often form the backbone of large and small organisations alike. They may enjoy being in charge of office filing systems, and using computers and other office equipment to keep things running smoothly. They usually like routine work hours and prefer comfortable indoor workplaces.
Clinical trials scientists need high levels of scientific knowledge and an interest in the reaction of diseases to drugs. The management of trials also requires good supervisory and organisational skills. Patience is important, as is the ability to take a long-term view.
You need to be able to think logically and analytically. You also need to be thorough and possess good information management skills. Report writing skills and an eye for detail are also important.
Entry Requirements - Clinical Trials Scientist
Pay & Salary - Clinical Trials Scientist
Salary Range (thousands per year)* 28k - 90k
Clinical Research Officer: 30 - 50
Clinical Data Manager: 35 - 70
Clinical Data Co-ordinator: 28 - 40
Manager - Clinical Trials/Operations: 35 - 90
Sigmar / Brightwater / CPL
Last Updated: March, 2017
* The lower figures typically reflect starting salaries. Higher salaries are awarded to those with greater experience and responsibility. Positions in Dublin sometimes command higher salaries.