I believe in building a team. Each member of the team should be clear on their role, know where they fit in and feel as though they can depend on one another. I also believe in real-time feedback. If you do something wrong you should know it immediately. Regardless of right or wrong, the further removed feedback is in time, the less effective it is. Answer tips: Speak about specifics that relate to the position you are applying for.
If you know you do not have much experience in the job you are applying for, plan for this question ahead of time and ensure you can provide some relatable examples based on what you have done. Almost all interviewers will appreciate confidence and pride in the work experience you have earned and your passion in transfering these valuable skills to your future role or position. Back then, it was obviously about earning some spending money. I then worked as a junior computer tech in my last 2 summers of high school.
It was here that I discovered what I was passionate about and what I wanted to do. I enrolled in college to get my degree in computer sciences, and I have been working around technology ever since. Answer tips: Here is an opportunity for you to showcase a wide variety of things you may have done both personally and professionally that will get your potential employers interested. Be sure to think about this one in advance in the event that it comes up.
Keep in mind, one of the key things that employers look for is an applicant who is self motivated and goal oriented. Again, this shows your employer you are the go-getter they are looking for. In the end, you want to ensure that you are leaving your interviewer with the impression that you are motivated, self sufficient, and manage your time effectively.
Answer samples That is a really great question. This has taught me a great deal about community, teamwork, and taking initiative. I took it upon myself to enroll in a summer business admin course at the local community college. Through this, I picked up some really great knowledge on communication and teamwork, as well as further develop overall managerial skills.
Though it may not be directly applicable to this particular job, I believe the overall experience I gained could be a real asset here. Your interviewer will use this as an icebreaker, ideally to put you at ease and get you speaking openly and honestly. The person giving the interview has a job to do as well — respect their time. Unless you are asked about something specific, focus on your education, your work history, relatable hobbies and outside interests, as well as your current situation.
Be sure to start chronologically and tell a linear story. Anonymous Answer "I like to be busy and productive; I check my calendar and always update it accordingly.
Rachelle Enns wrote: "Very carefully! I prioritize deadlines and work that needs to be done, then work backward from there. When necessary, I utilize my resources and team to pitch in and contribute. To prioritize, I make lists with to-do items and how long I think they'll take. That way, I know what needs to be done first and what small to-dos I can squeeze in in between the larger tasks.
I find it an effective way to manage my time and get things done when I'm busy. I am always sure to block things out on my schedule as needed, and love to follow a project management system, too. Something as simple as my calendar on my phone with alarms reminding me of what I'm supposed to be doing and when is helpful. I love to be busy and get things done!
What is your strongest skill as a Clinical Researcher? How to Answer The interviewer would like to know what you consider your greatest strength as a clinical researcher. Anonymous Answer "I excel in a few areas, but I would say my greatest strength in clinical research has been my ability to think critically and analyze the root cause problem.
Good answer. Rachelle Enns wrote: "In the past, I have received regular positive feedback on my ability to manage multiple projects while keeping consistent and accurate data. If I had to choose my strongest skill as a clinical researcher, I would choose my ability to multitask. I am a sponge for information at this point in my career and truly want to learn.
I am excellent with accepting, and implementing, feedback. When data is coming from multiple channels, it can be challenging to bring it all together to support a single hypothesis. I have been successful in working with complex data sets. Are you more interested in the statistics in research or do you prefer to get straight to the answer?
How to Answer It is important that the interviewer see that your work style is a good fit for their clinic's management style. Rachelle Enns wrote: "Although I have a strong appreciation for statistical analysis and the amount of work that comes with gathering that data - I crave the feeling of accomplishment that comes with getting to the conclusion.
I love the challenge that comes with taking the data and working it in a variety of ways. If I can dig into the data and then dig deeper, I can usually get to a place where the data will very clearly guide our research towards an outcome.
It's a fascinating part of being a clinical researcher. Which industry related current event interests you the most? How to Answer The way in which you answer this will be an indicator of your engagement level when it comes to this industry and your career. Anonymous Answer "I read up on current events in clinical research on a daily basis. Rachelle Enns wrote: "I am so happy you asked me that!
I was recently reading an article on how some hospital academic departments are starting to employ clinical research associates in clinical trial units and I would love to know what your thoughts were on this?
As a student, I did a study abroad semester in this region of the world and worked in a clinic that taught malaria prevention strategies. It was such an eye-opening experience for me, and I have been researching this topic ever since.
I recently read a fascinating article surrounding researchers from the Queen Mary University of London. They have successfully modified a flu virus and used it to target pancreatic cancer cells.
In your opinion, what is the most important factor in each phase of a clinical trial? How to Answer The interviewer is going to gauge your level of expertise in clinical trials based on the knowledge and confidence you display when answering this question. Rachelle Enns wrote: "Firstly, I believe it is important to not move onto the next phase of a clinical trial until the objectives of the current stage are met. In Phase 0, the most critical factor is to determine that the effect of the drug on the participant is as expected.
In Phase I, evaluating the safety and proper dose is the most important factor. For Phase II Without a strong base of safety, no trial can be published without question. The first is excitement and curiosity for how the project may impact the world.
The second is focused on the process and timeline of the clinical research plan. I think it's important to have the steps mapped out so that the team can stay on budget and on time. What steps do you take to ensure the safety of your participants during a clinical trial? How to Answer TThis answer is best to be given in a more factual manner.
Anonymous Answer "Having the medical background, I have learned that participant safety must come before all other factors. Rachelle Enns wrote: "The method of control I would use in order to ensure patient safety may depend on the phase of the trial we are in. For example, if we are in Phase I of the clinical trial I would keep a very close eye on the participants and watch for any serious side effects.
Documentation is incredibly important as well. Also, if there are any instructions for the research patients, I always ensure that they understand those instructions explicitly. I check in regularly. This includes taking proper documentation, ensuring participants understand their instructions and the risk of participation. Also, a keen eye for all patients is imperative. In my years of experience, I have also gained confidence to raise any concerns with my supervisor if something comes up that feels like it needs further safety consideration.
Tell me about a study that you dream of participating in, one day. How to Answer The interviewer is asking this question in a friendly way to figure out what type of research is closest to your heart.
Anonymous Answer "My father was diagnosed with cancer in his late 70's and I have always been passionate about research related to that disease. Rachelle Enns wrote: "I have a firm interest in studying childhood depression. I have a younger sibling who suffered from severe childhood depression, and the topic has always been close to me.
If I could offer something to that area of study, that would be very fulfilling work for me. I have always been interested in learning more about the disease and seeking alternative forms of treatment.
I have been reading about the medical advancements for years, but I think there is more work to be done.
That would be a dream project for me. My dream research project would be in early detection and prevention of Alzheimer's. Have you ever been part of a clinical investigation led by the FDA due to non-compliance? How familiar are you with GCP standards and practices? Rachelle Enns wrote: "The company I currently work for has an incredibly high standard when it comes to good clinical practice. Fortunately, I have never worked for an employer that has been in non-compliance with FDA standards.
In my current position, I train new researchers on our GCP standards so I would rate my knowledge as expert level. I pride myself on being highly ethical and would not hesitate to reach out to a superior should I have doubts about the required standards and practices.
How to Answer The interviewer is looking for your range of experience and understanding of Standard Operating Procedures. Anonymous Answer "I understand that writing an SOP requires a strong understanding of procedural tasks and activities. Rachelle Enns wrote: "I have approximately three years experience writing SOP for two different clinics.
I would describe my level of experience in intermediate. For example: "I understand that writing an SOP requires a strong understanding of procedural tasks and activities.
Although I do not have specific experience to show, I am confident that I could write new Standard Operating Procedures once I have a complete understanding of the clinical trial or program. I have created four sets of SOPs in response to compliance issues as well as assisted researchers with creating SOPs in the past. I could teach this skill and would say that my level would land in the expert range.
When would you be available to start? How to Answer Before your interview, make sure you have a start date in mind for the new employer. Rachelle Enns wrote: "As a professional courtesy, I would like to give my current employer two weeks' notice.
I could start anytime after that. But, out of courtesy to them, I need to let them make the decision. Due to my length of employment, it is possible that I may need to work an additional week if they were to request it of me to aid in the transition to the next clinical research manager, but I am available immediately following.
Can you clarify your timeline for me? We receive a great deal of private funding which requires us to keep very close track or our spending. Outline your experience in budget management and resource allocation.
How to Answer Most clinics are required to be very transparent with their spending. I achieved this successfully through careful planning and financial analysis in 'Program XYZ'. I am comfortable with all budget related tasks. I saw in your job posting that this role will have a large part in assisting with budget management. This is exciting to me, and I look forward to learning from your senior team members. While this is not the largest budget that I have managed, I can clearly estimate expenses, determine the project timeline and allocate resources within budget.
In your career, which research projects have you taken the most initiative on? How to Answer Your answer to this question will reveal to the interviewer your biggest areas of interest and where you strengths stand out during a research project or clinical trial. Rachelle Enns wrote: "I am new to my career as a clinical researcher and have not yet been given the opportunity to take the lead on a research project.
I did; however, take the lead on a couple of group projects while completing my Bachelor's degree in Life Sciences. I brought one of my proudest projects with me today so that you could see my work.
It's a research project on the link between obesity and mental health. Would you like to take a look? I thought up a partnership with a local nursing home that allowed us to survey patients before and after their dialysis treatments and monitor their emotional states. This ended up being the most important data collected in the research.
Can you tell us a time when you took on additional responsibilities? How did you successfully manage to meet the demand for these responsibilities? In your experience, what is the key to ensuring that your company was compliant with policies and procedures? Share with us your approaches to handle this data. Describe your experience collecting blood and tissue samples from patients.
Describe a time when you effectively fixed, adjusted, or tested an electronic device or machine. If you realized during a site visit an ADR was not reported to the sponsor within 24 hours, what do you do? From your perspective, what is the key to developing a good team? When job- hiring asking this question, basically they want to know how to balance your work-life relationship.
Traveling for work might create lots of challenges. However, managing them brings many benefits to you. Tell the interviewers how to overcome these challenges by adapting some strategies. When the company has well-trained employees, the business will run more smoothly. The knowledgeable staff can perform their job with greater competency, serve their customer better, and bring prosperity to the company. While training employees can bring success to the company, an un-structural and time-consuming program can have a negative impact on company productivity.
Your response will be focused on how you train your staff in an effective way and make good use of the hours. Frequent training maintains the skills and knowledge of individuals. In your experience, what are the keys to ensuring your company was compliant with policies and procedures?
Effective policies and procedures take lots of time and energy to be established and enforced. The policies and procedures to be efficient need specific methods to measure the understanding of the employees and the right amount of collaboration between the company members. To ensure that all members of your company comply with your policies and procedures, you have to follow these strategies:.
This is one of the popular questions CRA often asked. One of the main responsibilities of CRA is data submission, verification, and completeness. Job hiring wants to know the approaches you can take to extract useful information from large datasets and how you deal with security issues. While dealing with large data sets is sometimes overwhelming, there are many effective strategies you can follow to make your data analysis more efficient.
If you worked in big data you probably know some of them. Explain Verification? Answer : Verification ensures the accuracy of the final tables and the quality of SAS programs which generates the final tables. Question 8.
Question 9. Answer : Demog: Body mass index is below expected and Weight is outside expected range. DOB is greater than the Visit date or not. Age is not within expected range. Visit Start is before birthdate or Stop is before the start. Study medicine discontinued due to the adverse event but completed. Answer : Pharmaceutical companies spend several months to conduct longitudinal studies on human subject. It is unrealistic to expect patients to keep timely visit over such a long period of time.
Despite all the efforts, patient data are not collected for some and these become missing values in a SAS data set later. For reporting, the most recent previously available value is substituted for each of the missing visits. Also if there are multiple variables containing these values then they will be carried forward independently.
They supervise informed consent forms for clinical trials, case report forms and design and writing of protocols. Question What Is A Clinical Trial? Answer : Clinical trials, also known as clinical studies, test potential treatments in human volunteers to see whether they should be approved for wider use in the general population. A treatment could be a drug, medical device, or biologic, such as a vaccine, blood product, or gene therapy.
Potential treatments, however, must first be studied in laboratory animals to determine its safety before they can be tried in people. Treatments having acceptable safety profiles and showing the most promise in the animal model are then moved into clinical trials.
Clinical trials are an integral part of new product discovery and development, and are required by all regulatory agencies e. Participants in clinical trials play a key role in drug development and discovery;. First and foremost participants can help others by contributing to medical knowledge and improving public health. Further, a participant does not need to be a patient diagnosed with a specific disease or health problem as some clinical trials, focusing on safety, will include healthy volunteers.
Patients who take part in clinical trials may benefit from the treatments they receive. As part of a clinical trial, a patient will receive either the experimental treatment being tested, an accepted standard treatment for the condition, or a placebo.
It is important to understand that there is no guarantee that any treatment received in a clinical trial will produce the desired results. Answer : For all types of trials, participants work with a research or clinical trial team, including doctors, nurses, social workers, and other health care professionals.
Prior to the trial, the research team will check the health of the participant and review any special instructions for trial participation. As the trial begins and throughout its duration, the research team will administer treatment, whether that be the experimental treatment, a standard treatment or a placebo depending on the requirements of the study and monitor the participant on a regular basis to determine effectiveness and side-effects of the treatment.
Ongoing communication is an important part of any clinical trial and after the trial has been completed the research team will stay in touch with the participant for a specified period of time to assess any effects of the treatment after treatment has stopped.
What Is Informed Consent? Prior to enrollment in a clinical trial, researchers inform participants about all relevant study details and known risks.
Participants are then provided an informed consent document that details all the important study information including its purpose, duration, risks, potential benefits, required procedures, and key contacts.
Once participants have had a chance to read this form and ask questions, if they agree to participate in the trial,they will be asked to sign an informed consent document. The informed consent document is not a contract. The research team actively maintains informed consent throughout the entire trial by providing the participant with any new or developing information, as needed.
Answer : Before joining a clinical trial, a participant must meet certain criteria. This is an important aspect of any clinical trial to ensure that the treatment is being investigated accurately and safely. Factors that allow someone to participate in a clinical trial are called "inclusion criteria," and those that disallow someone from participating are called "exclusion criteria. These criteria are used to identify appropriate participants.
Acceptance of a participant into a clinical trial is based on such factors as age, gender, the type and stage of disease, previous treatment history, and other medical conditions.
For example, some research studies seek participants with specific illnesses or conditions, while others need healthy participants.
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