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Clinical scientist skills for your resume and career
15 clinical scientist skills for your resume and career
1. Patients
- Supported identification of mutations/susceptibility factors impacting treatment of patients with cancer (large patient population).
- Participated in analysis of collected data from cancer patients.
2. Informed Consent
- Experienced in performing informed consent, preparing study documentation, obtaining clearances/approvals, designing studies and handling adverse events.
- Participate in protocol development, generation of standard informed consent and other related study documents and forms.
3. Clinical Operations
Clinical operations caters to the administration of the drug development process by ensuring there is proper planning, appropriate conduct through the process, safety of patients and use of quality data. It also encompasses facilitating effective communication between the different study sites and sponsors of the drug process.
- Assist with site feasibility and the identification/selection of qualified investigators and study sites in collaboration with Global Monitoring/Clinical Operations.
- Participated as the U.S. clinical operations representative for all international cardiovascular research programs.
4. Oncology
Oncology is defined as the facet of medicine that deals with cancer. Oncology also deals with the prevention and diagnosis of these diseases. A medical professional who has studied the discipline of oncology is referred to as an ‘oncologist'. An oncologist can further specialize in their discipline and become a medical oncologist, surgical oncologist, or radiation oncologist.
- Coordinated the release of client medical records and create detailed summary forms of clients' oncology and medical histories.
- Interact with investigators and thought leaders in oncology to facilitate the design of clinical synopses and protocols.
5. Clinical Development
- Developed contingency plans, clinical development plans to meet challenges necessary to execute business and study action plans.
- Project Manager for major domestic & international cardiovascular clinical development programs.
6. Clinical Data
- Provided quality control of clinical data in abstracts, posters, presentations and other scientific and educational materials.
- Supervised/Chaired clinical data review meetings consisting of Medical Monitor, PV and data management groups.
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Google Cloud Platform (GCP) is a collection of cloud computing services that allow users to develop, deploy, and operate original applications on the web. GCP carries a cloud computing infrastructure that facilitates it in keeping track of the resources (e.g., storage, processing speed, and power, network connectivity, database queries, etc.) of an application or a website, whenever it is run on the cloud platform.
- Ensured compliance with current regulations in US and EU including Safe Harbour, GCP, HIPAA, and Sunshine Act.
- Lead clinial trials in phase I, II and III in accordance with GCP and ICH guidelines.
8. Data Management
The administrative process that involves collecting and keeping the data safely and cost-effectively is called data management. Data management is a growing field as companies rely on it to store their intangible assets securely to create value. Efficient data management helps a company use the data to make better business decisions.
- Perform reconciliation of clinical trial adverse event data captured in Clinical Safety and Data Management databases.
- Interacted with MDM (medical data management) and performed database reconciliations involving study projects.
9. Clinical Trials
- Prepared and executed cosmetic clinical trials according to written protocol, using Good Clinical Practices.
- Participated in the selection of investigators and contract research organizations to conduct clinical trials.
10. Data Analysis
- Coordinated kick off meetings, monitored metrics, monitored logistics, provided interim data analysis and reporting.
- Maintained and managed source documents, ensured quality of data, performed data analysis and made epidemiological interpretations.
11. Biostatistics
Biostatistics is the development and implementation of a wide variety of topics in biology. It includes the design of experiments, collection, and analysis of data. The primary use of biostatistics in medical research is investigating a problem through a scientific technique. The data derived from the study is nominal, interval, and ordinal data.
- Interacted with Biostatistics and Operations to develop protocols including statistical sections.
- Validate and transfer external vendor data to the Biostatistics Unix platform.
12. Project Management
- Participate in trial committee (Project Management, Data Project Management, Clinical Assay Sub Team, etc.)
- Managed study budget and timelines, and maintained accurate study information in the clinical trial database CTMS and project management systems.
13. ICH
- Adhere to government regulations, ICH and FDA guidelines, and company SOPs when executing assignments.
- Performed study management in conjunction with FDA regulations, ICH guidelines, and company SOPs.
14. Regulatory Submissions
Regulatory Submissions offers a readable and clearly written road map for effective submission of documents for required regulatory reviews during product development.
- Prepared clinical study reports for regulatory submissions.
- Audited, collected, tabulated, and analyzed clinical data as required to support technical reports, publications and regulatory submissions.
15. FDA
The Food and Drug Administration (FDA) is a division of the US Department of Health and Human Services that regulates the production and sale of food, pharmaceutical products, medical equipment, and other consumer goods, as well as veterinary medicine. The FDA is now in charge of overseeing the manufacture of products like vaccines, allergy treatments, and beauty products.
- Work with sites to ensure their IRB approvals and FDA form 1572 are updated and current.
- Reviewed serious adverse event reports received from other local country sectors for expediting to the FDA.
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What skills help Clinical Scientists find jobs?
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What clinical scientist skills would you recommend for someone trying to advance their career?
What type of skills will young clinical scientists need?
Professor, Pharmacology & Toxicology; Professor, Obstetrics & Gynecology, Wright State University
Some were even given a test to see if they understood the concept. This then leads to mass spectrometry, LCMS, MALDI-TOF, and even GCMS, and everything that has been developed around those basic techniques is now commonplace in most core facilities and Pharma. New methods for flow cytometry, FACS, are necessary for the higher throughput drug discovery types of labs. Molecular biology has evolved from simple PCR machines that could run 24 samples, just 25 years ago, to digital PCR machines that can run 384 pieces today and email the final data to you at home, while you sleep. Knowing how to calculate the PCR data is extremely critical, as it isn't intuitive, and people tend to take short cuts. Knowing how to do that will be vital. Cell culture and working with animals are still common ways to generate data in any lab, and people who have those skills will always have a job. What do all these techniques have in common? They all have evolved to the point that no one is an expert in every one of them. Labs focus and concentrate on the ones they need the most and make use of them over a long period. What a student should develop is what I call a big toolbox. Learn as many of these techniques as you can, and then use them. Understanding that these are all cyclic and that you may get rusty, or the technology will change. It doesn't matter. By being trained in any of these, it will mean that you can be prepared for other things, that you can catch up and learn and update your techniques in your toolbox. This is what any PI running a lab will be looking for, someone who can be trained, and can evolve and adapt to different technologies, know how they work and how they can be used, what the data looks like when it is working well, and what it looks like when it isn't. The people who have these skills will always be employable.
There is a greater need than ever for workers to analyze data and synthesize a reasonable idea about what it means. This means that they must understand their experiments at a deeper level than just pipetting buffers and timing reactions. They must know what is happening, and if there is a problem, first, they have a problem and then how to solve it. Bioinformatics has become one of the fastest-growing fields. The increased amount of data, whether from standard assays run in an ordinary lab or high throughput data, needs more crunching. The future researcher will not be able to get by just knowing how to use a computer stats program but will be required to understand how to run data in R or Python or whatever new data analysis package is coming next. This becomes even more critical as the data becomes more complex, i.e., 27 cytokines analyzed in 3 different tissues over three other times, from 14 different groups, 6 of which are controls, with the rest being toxin and then treatment groups and authorities. A simple two way ANOVA just doesn't cut it. For this, machine learning tools, pattern recognition, neural networks, topological data analysis (TDA), Deep Learning, etc., are becoming the norm and are being advanced and changed to give more and more substance to what the data means. Students who can operate instruments to generate data and run more complex types of analysis on this 'big data' are in great demand. Likewise, learning the computer-generated design of drugs 'in silico' is a growing field that is now required to screen tens of thousands of compounds before generating them in the lab. This will need someone who can think three-dimensionally; even though the software and advanced computers can do that, it helps if your brain is wired that way, at least a little.
Aside from instruments and complex data analysis, consider where the clinical research is headed. With COVID19, the need to quickly advance drugs from potential use to clinical application has undergone an exponential increase. Lives are being lost daily to the lack of a vaccine or medication that can attenuate to any level the impact the virus has on the human body. The future clinical researcher will need to understand how the instruments work and how tests are run, how a vaccine works, how the virus or disease manifests itself, and how to get it under control. This will only be possible if the researcher is familiar with much of what I wrote above. You won't need to be an expert on virtually everything, but you'll need to understand it so you can use it to synthesize new ideas that may be applicable in the clinical environment. COVID19 is a perfect example. One of the early struggles with this virus was how to test for it. Antibodies weren't developed for it in the very beginning, so an ELISA was out.
In contrast, PCR is one of the most sensitive methods to identify genetic material, such as viruses. So, early on, PCR primers were created that could be used to run a PCR to determine if a person had a live virus. However, the first such PCRs had high false negatives and positives. Further refinement led to the creation of PCR primer sets and protocols that allowed for a more accurate and faster test. An advantage that anyone who has been trained in biotechnology will know the basics of developing a test. If it is a PCR, then what goes into that. Suppose it is an ELISA, how it works, and what you need to set it up. Imagine a test strip similar to the one used for at-home pregnancy tests. This came about in much the same way, through experimentation and developing a way to lower the false negatives and positives, to allow a quick, 5-minute test that could determine if a particular hormone was in your urine at a stage of pregnancy when many women may not have realized there was a possibility they could be pregnant. The person entering the workforce that can think in these ways will be employable and will be able to move between jobs and continue with a very successful and enriching career.
What technical skills for a clinical scientist stand out to employers?
Sharolyn Kawakami-Schulz Ph.D.
Director, Office of Professional Development, University of Minnesota Medical School
What soft skills should all clinical scientists possess?
Associate Professor, Assistant Dean for Graduate Academic and Student Affairs, SGS, School of Graduate Studies, Rutgers University
List of clinical scientist skills to add to your resume

The most important skills for a clinical scientist resume and required skills for a clinical scientist to have include:
- Patients
- Informed Consent
- Clinical Operations
- Oncology
- Clinical Development
- Clinical Data
- GCP
- Data Management
- Clinical Trials
- Data Analysis
- Biostatistics
- Project Management
- ICH
- Regulatory Submissions
- FDA
- Data Review
- Cros
- Clinical Study Reports
- Clinical Pharmacology
- Study Protocols
- Safety Data
- Study Design
- Data Collection
- Medical Writing
- IND
- NDA
- Investigator Brochures
- Pharmacokinetics
- Biomarkers
- Pharmaceutical Industry
- Site Selection
- Study Sites
- PK/PD
- External Vendors
- Consent Forms
- IRB
- Phase II
- Clinical Safety
- CRF
- Research Projects
- CRA
- QC
- Clinical Sites
- Hypertension
- GLP
- Clinical Trial Management
Updated January 8, 2025