#Clinical Data Management training

[pharmaconnections01]

The Advantages of Clinical Data Management Training: Unlocking Opportunities in Healthcare - Pharma Connections

Explore the advantages of clinical data management training with Pharma Connections. Learn how online courses can boost your career, unlock opportunities in healthcare, and contribute to the ever-evolving clinical data management industry.

[greatonlinetrainingsposts]

The Future of Clinical Data Management

Clinical data management (CDM) is essential for clinical research, and the increasing complexity and volume of data generated by modern trials require new strategies and tools to manage it efficiently.

Artificial Intelligence (AI) and machine learning have the potential to revolutionize clinical data management by automating data entry, cleaning, and validation, and identifying patterns and trends in the data. AI can also help identify adverse events and predict patient outcomes.

Blockchain technology has the potential to increase security and transparency of clinical trial data by providing an immutable record of data transactions. It can also help with data sharing among stakeholders, while maintaining data privacy.

Cloud-based solutions offer improved scalability and flexibility in managing clinical trial data, allowing for real-time data access, sharing, and analytics across multiple sites, enabling faster decision-making and more efficient clinical trial management.

Wearable devices and sensors are becoming increasingly popular in clinical trials, generating large volumes of continuous and real-time data. This poses a challenge to traditional data management systems, so new strategies and tools are needed to manage and integrate these data streams.

Data visualization and analytics tools are becoming increasingly important due to the increasing volume and complexity of clinical trial data. They help researchers visualize and analyze data, identify patterns and trends, and make better-informed decisions.

Patient engagement has become increasingly important in clinical trials, with tools such as collecting patient-reported outcomes, facilitating informed consent, and allowing patients to access their own clinical trial data. This increases transparency and trust in the research process.

The future of clinical data management lies in the integration of new technologies such as AI, blockchain, and cloud-based solutions, as well as the development of patient engagement tools, wearable devices, and sensors. It is essential to develop innovative and efficient strategies and tools to manage and analyze these data effectively.

If you are seeking Clinical data management Training in the United States, India, Nigeria or anywhere else in the world, you must contact Great Online Training.

[companysconnectsin]

Steps to stay updated on the drug regulatory changes

Get more info at https://www.companysconnects.com.

[igmpi]

Our Clinical Research Course offers a detailed curriculum covering essential aspects of clinical research, including methodologies, regulatory requirements, and industry best practices. This course is designed for individuals aspiring to pursue careers in clinical research or seeking to enhance their existing skills in the field.

[problogsposts]

Why Should You Consider a Career in Medical Coding?

Introduction

Are you looking for a rewarding career in the healthcare industry that doesn't require years of medical school? If so, medical coding might be the perfect choice for you. In this blog, we'll explore the exciting world of medical coding, its importance in clinical research, and why you should seriously consider it as a career option. Let's dive in!

What is Medical Coding?

Medical coding is like the language of healthcare. It involves transforming medical information such as diagnoses, procedures, and treatments into universal codes. These codes are used for various purposes, including billing, insurance claims, and clinical research. Essentially, medical coders are responsible for ensuring that the healthcare system runs smoothly by accurately documenting patient records.

Why Choose a Career in Medical Coding?

1. In-Demand Career: The healthcare industry is constantly growing, and with it, the demand for skilled medical coders. Hospitals, clinics, insurance companies, and research institutions are always in need of qualified professionals to handle their coding needs.

2. Short Training Period: Unlike many other healthcare careers that require years of education, you can become a medical coder relatively quickly. Numerous institutes offer courses and training programs in medical coding that can be completed in a matter of months.

3. Diverse Opportunities: Medical coding isn't limited to just one type of job. You can find opportunities in various settings, including hospitals, private practices, pharmaceutical companies, and research organizations. If you want to explore related fields, you can also transition into areas like pharmacovigilance, drug regulatory affairs, or clinical data management.

4. Stability and Job Security: The healthcare industry is known for its stability, and medical coding is no exception. As long as there are healthcare services, there will be a need for medical coders. This translates to job security and peace of mind in your career.

5. Work-Life Balance: Many medical coding jobs offer excellent work-life balance. You'll typically work regular hours in a comfortable office setting, allowing you to maintain a healthy work-life balance.

6. Good Earning Potential: While salaries can vary based on location and experience, medical coders generally earn a competitive wage. With experience and additional certifications, you can increase your earning potential even further.

7. Contributing to Healthcare: By ensuring accurate coding, you help maintain the integrity of patient records, improve patient care, and support clinical research, pharmacovigilance, drug regulatory affairs, and clinical data management.

The Role of Medical Coding in Clinical Research

Now, let's delve into the connection between medical coding and clinical research. Clinical research plays a vital role in advancing healthcare treatments and therapies. It involves testing new drugs, medical devices, and treatment protocols to ensure their safety and effectiveness. Medical coding is an essential part of this process for several reasons:

1. Data Accuracy: Accurate coding ensures that the data collected during clinical trials is reliable. Researchers rely on this data to make informed decisions about the safety and efficacy of new treatments.

2. Regulatory Compliance: Regulatory agencies, such as the FDA, require precise documentation of clinical trial data. Medical coding helps maintain compliance with these regulations, which is critical for getting new drugs and treatments approved.

3. Patient Safety: Proper coding helps identify any adverse events or side effects experienced by patients during clinical trials. This information is crucial for patient safety and determining the risks and benefits of a new treatment.

4. Data Analysis: Medical coding simplifies the process of data analysis by categorizing information into standardized codes. This makes it easier for researchers to identify trends and draw conclusions from the data.

How to Start Your Career in Medical Coding?

1. Take a course: Look for reputable institutes or online courses that offer medical coding training. These courses cover topics like anatomy, medical terminology, and coding systems such as ICD-10 and CPT.

2. Get Certified: While certification isn’t always required, it can significantly boost your job prospects. Consider obtaining certifications like Certified Professional Coder (CPC) or Certified Coding Specialist (CCS) through recognized organizations.

3. Gain Experience: Entry-level positions may require some on-the-job experience. Look for internships or entry-level coding jobs to build your skills and resume.

4. Stay Updated: Medical coding guidelines and regulations can change, so it’s essential to stay current. Attend workshops, and seminars, and continue your education to remain competitive in the field.

5. Network: Join professional organizations such as the American Health Information Management Association (AHIMA) or the American Academy of Professional Coders (AAPC) to connect with other professionals in the industry.

Conclusion

In conclusion, a career in medical coding offers stability, good earning potential, and diverse opportunities within the healthcare industry. Moreover, it plays a crucial role in clinical research, contributing to the development of new and better treatments for various medical conditions. If you're interested in healthcare, have an eye for detail, and enjoy working in a structured environment, medical coding could be the perfect career choice for you. Consider enrolling in a reputable training program or course to kickstart your journey into this rewarding field. Your future as a medical coder awaits!

[clinosolresearch]

DATA VISUALIZATION IN CLINICAL TRIALS

"Data plays a key function in organizing, monitoring, and analyzing findings for a clinical study, similar to the foundation of a new house. Data provides new insights, helps evaluate hazards, and helps choose the best course of action for a study.

Introduction

In clinical trials, adverse events are often reported by simply counting the number of people who experienced each event. Reporting only frequency leaves out other data aspects that are crucial for stakeholders, such as severity, seriousness, rate (recurrence), timing, and groups of connected Adverse events. Data visualization is the process of displaying data in such a way that it can be easily understood. It helps to identify patterns and trends and make decisions based on this information. A good data visualization tool will allow you to quickly summarize your data and make it easy for others to understand what it means.

In the last ten years, there has been an increase of 183% in data per clinical trial because of breakthroughs in science and technology. The amount and variety of such data have grown well beyond what a straightforward spreadsheet can handle. The volume and variety of data generated by clinical trials will increase as they adopt decentralized methods. The main obstacles for sponsors of all sizes are importing and evaluating data from wearables, imaging systems, apps, and central labs. The importance of curating and delivering the data to stakeholders is growing along with the difficulty and time commitment. To complete these responsibilities, a platform that enables research teams to access all data in one location is now essential.

What is Data visualization?

Data visualization is the graphical representation of information and data using visual elements like charts, graphs, maps, and other visuals. It uses a variety of techniques, such as graphs and charts, pie charts and bar graphs, line graphs (to compare two sets), maps, timelines (to show repeated observations), histograms (to find outliers), box plots, etc.,

Comparison of traditional frequency tables and data visualization

Data visualization is more effective than frequency tables because it allows you to compare data more intuitively. A traditional frequency table shows how many times each option was selected but does not allow you to see any other information about the response (e.g., mean, or median). This can be time-consuming if multiple options are being compared or if many different metrics are being displayed on one page with no space between them

Power of Data Visualization

Traditional methods just don't allow for efficient use and administration of that data when the volume of data increases and decentralized trials become more prevalent. You may easily integrate, organize, and analyze clinical data using visualization tools to boost operational effectiveness and drive clinical trial success. In addition to the obvious benefit of being able to identify outliers and trends, data visualization also helps with identifying clusters, correlations, and relationships. These are all ways that you can use your data to inform decisions about a trial.

Benefits of data visualization

More informed decisions

Faster analysis 

Improved organizational efficiency 

Visualizations can better support investigators to assimilate large volumes of data and enable improved informal between-arm comparisons compared to tables

Increased competitive advantage

Improved customer experience

Visualization can show data quality issues, support robust temporal searches, or even discover cohorts of patients meeting selection criteria for clinical studies that depend on huge warehouses of patient data.

The availability of more internet information and personal sensors has begun to raise patient awareness of and ownership over their health. This is a significant departure from the paternalistic approach to healthcare in which patients trust their doctors with their health during annual checkups or in the event of an injury or illness.

Provide insights into the relationships between variables and help you identify potential flaws in your study design.

Conclusion

Data visualization is a powerful way to improve the quality of Clinical trial data. The use of tables, dot plots, and volcano plots can encourage differing interpretations. This can be achieved by providing interactive tools for data exploration and analysis, as well as visual displays that are easy to interpret and understand. Care in the construction of visual displays needs to be taken as there can be potential to overemphasize treatment effects in some circumstances.

https://www.clinosol.com/

[octovion]

Clinical Data Management Online Training Course with Placement

The demand of clinical professionals is growing rapidly making it an interesting career option with massive growth potential. This particular technology of Clinical Data Management has become one among the top fields currently as if you have done the training properly and professionally with experts, you will be hired by top notch companies with ease as the demand for the clinical SAS candidates are on high right now.

Clinical data management training heavily emphasizes ethics in research as well as the regulatory aspects of clinical data collection, data management, and drug development. The course syllabus is structured based on expert’s knowledge and experience. It will help you survive in the current industry. Here are the common course modules where training providers teach you.

Introduction to Clinical Research

Basic Pharmacology and Pharmacy in Clinical Research

New Drug Development

Ethical Guidelines in Clinical Research

Ethics in Clinical Research

Regulations in Clinical Research

Biostatistics in Clinical Research

Specialist Clinical Trials and Clinical Trial Designs

Clinical Trial Documentation

Quality in Clinical Trials

Clinical Data Management

Clinical Trial Management

Drug Safety and Pharmacovigilance

Soft Skills for a Clinical Research Professional

Who can take up the Training?

Life science graduates

Biomedical engineering

Who have keen interest in Medical sciences

Anyone having Health Care Background

Interest in Clinical Research

Skills required by the employers for Clinical SAS placements:

Clinical Trials knowledge

Collaboration

Able to handle the project swiftly with excellent communication skills

Very good analyzing skills

Team Player

Job Roles in the Clinical SAS Industry

Junior Level Clinical Research Associate CDM

Senior Level Clinical Research Associate CDM

CDM Industry Statistics and Standards

1K Jobs Per Month

Minimum Salary from 50K USD Per Annum in USA

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Best Clinical Data Management Course in Pune - Lifepoint Research

When clinical trials are conducted, a huge amount of data gets generated. But how is this data collected and managed? Lifepoint provides the best clinical data management course in Pune

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Scope and Responsibilities of Clinical Data Management

Clinical data management (CDM) is a critical phase in clinical research that ensures high-quality, reliable, and statistically sound data from clinical trials. It also supports the conduct, management and analysis of studies across the spectrum of clinical research as defined by the National Institutes of Health (NIH). The ultimate goal of CDM is to assure that data support conclusions drawn from research, protecting public health and confidence in marketed therapeutics.

CDM is the entry, verification, validation, and quality control of data gathered during clinical trials, and India is the second most preferred destination due to its large patient pool, faster enrollment, and low cost. Our Great Online Training offers the best Clinical Data Management Training in Hyderabad, India, USA, and Nigeria.

Scope of Clinical Data Management

Data Management positions involve managing and processing clinical trial data.

Statistical Programming is the use of statistical programming languages to manage, analyze and report clinical trial data.

Regulatory Affairs is responsible for ensuring compliance with regulatory requirements for clinical trials.

Project management is the process of managing clinical trials to ensure they are conducted on time, on budget, and in compliance with regulatory requirements.

Clinical Research Associate is responsible for ensuring the smooth running of a study and the quality of data collected.

CDM has a high demand for skilled professionals, with many job opportunities in the pharmaceutical, biotechnology, and medical device industries. The field is constantly evolving, providing opportunities for individuals to learn and grow in their careers.

Responsibilities of Clinical Data Management

Study set-up involves defining data specifications, creating data collection tools, data validation plans, data entry guidelines, and data quality control procedures.

Data collection and processing is essential for ensuring accurate, complete, and consistent data across all study sites.

Data quality control is the process of identifying and resolving data discrepancies.

Database management ensures data is entered, tracked, and maintained according to protocol and regulatory requirements.

Data analysis and reporting is essential for decision-making and regulatory submissions.

Study close-out involves reconciliation, archiving, and preparing data for long-term storage and reference.

CDM is responsible for ensuring the accuracy, completeness, and consistency of clinical trial data to support the safety and efficacy of new drugs and medical devices. It also ensures compliance with regulatory requirements and industry best practices.

[petrolstationflowers]

Up to your neck in true crime and feel you can really get into why burglars keep stealing your toilet? Then perhaps the Criminal Psychologist career is for you! This was another request from Catrillion and I had to do a fair bit of digging to make sure this one was accurate.

This job is available for YA - Elder, and you can join via the Police Station. Please note you will need University installed as one of the requirements is the Science skill!

No opportunities or books.

If you want to use this, you must have Nraas Careers installed for it to show up!

There are three custom tones to level your skills:

Build a Rapport (Logic) Write Your Report (Writing) Study Previous Cases (Science)

Coworker tones are the same, and skill tones and uniforms appear from level four. The carpool doesn't appear until level three -- you're a poor postgrad, after all!

Levels under here:

Positive Postgraduate - 10 simoleans p/h, 09:00 - 17:00, M-F Description - It’s been a long road to graduation – plenty of sleepless nights watching true crime documentaries and making flash cards for exams, because Watcher forbid you muddle up the Hansford Prison Experiment and the Toto Doll study. You’ve decided you want to jump right in and get an internship, but where to start? Better start cozying up to your professors and making some phone calls! Enthusiasic Intern - 15 simoleans p/h, 09:00 - 18:00, M-F Description - After laying on the praise and asking very nicely, you’ve managed to secure an internship for the year. The pay is nothing special and the hours are long, but you’re learning a lot, working at the local police station, accompanying jail, and the mental health unit over at Sunset Valley General. You’ll be profiling offenders and writing out risk assessments for those living with Unstable personalities, writing recommendations to make the prison nicer and holding therapy sessions. Better hope they’ve got good coffee! Criminal Psychologist In Training - 30 simoleans p/h, 09:00 - 18:00, M-F Description - If you thought you escaped the classroom, think again. Sure, you’re finally getting to put your skills to use, but while you’re still helping out at the precinct, you’re also trying to put together where your skills lie. Would you be best working at HMS Sunset Valley, overseeing prisoner rehabilitation, or in the interview room at the police station working on a report for Sunset Valley Plumbbob Court? Best find a quiet spot in the legal library and do some studying – oh, and your manager wants those reports by the end of the day.

Junior Criminal Psychologist - 40 simoleans p/h, 09:00 - 18:00, M-F

Description - You’re not quite working in the big leagues yet, but you’re getting there. You’ve been assigned to the psychiatric unit, triaging those who have been sent your way and helping out with various studies being conducted around the facility. You are, however, getting to sit in on diagnostic intakes and occasionally are being trusted to write up your own. Hopefully if you format the reports nicely enough, you’ll be allowed to steer the ship yourself.

Clinical Researcher - 70 simoleans p/h, 09:00 - 18:00, M-F

Description - Now you’ve found your feet, you’ve been assigned to work on a clinical research program. Sure, it’s only a contract job, but you’re learning about kleptomania and why certain sims are compelled to steal street lights. Lots of note taking, interviewing people, and staring at graphs until the numbers blur, but when you finally see patterns and correlations, it’ll all be worth it!

Treatment Psychologist - 80 simoleans p/h, 09:00 - 18:00, M-F

Description - The data about street lights proved fruitful, and the local government have decided that the results are valuable enough to be put into practice. Sunset Valley General has set up a specific ward for those suffering from kleptomania, and you’ll be setting up therapeutic workshops and treatment programs to try and cut down on their thievery. It’ll take time, patience, and empathy – luckily, you’ve got those in spades.

Psychologist - 100 simoleans p/h, 09:00 - 15:00, M-F

Description - Out on your own now, with an office and everything! No longer chained to a hospital or a ugly precinct storage room, you’re free to pursue topics that interest you and studies that make your brain light up. It’s back to assessing and evaluating patients, setting up group studies and making recommendations for them to take a long holiday to Barnacle Bay for the sake of their health. The hours are shorter and pay is better – maybe you’re finally at the top?

Senior Psychologist - 120 simoleans p/h, 10:00 - 17:00, M-F

Description - Business is booming, but there’s something missing; counselling snobby sims through their affluenza or prescribing pills for cowards who can’t stop running away from Bonehilda isn’t as fulfilling as it used to be. You’ve been keeping an eye on local job postings and there’s one that’s caught your eye; something about working with the police force to uncover exactly how their minds work. Perhaps it’s time to spruce up your CV…

Investigator in Training - 150 simoleans p/h, 09:00 - 18:00, M-F

Description - You’re back to long hours and endless studying, but this one is paid well and comes with lots of benefits; namely, finally getting to study some of SimNation’s most intriguing criminals up close. You’re not being turned loose quite yet, so for the moment you’ll need to shadow your fellow officers and write up dictated reports on just why you think the Tricou family died and who had the motive to arrange Bella Goth’s disappearance. Keep your nose to the grindstone and soon you’ll be free of hours long recordings and into the interrogation rooms yourself.

Criminal Investigator - 200 simoleans p/h, 09:00 - 18:00, T,W,U

Description - That work has paid off and you’re finally where you wanted to be – sitting across the table from some of the most dangerous people in SimNation. When Circe Beaker has been hauled in for illegal experimentation and Roderick Synapse has finally been arrested for kidnap, it’s your job to sit down with them and pick apart their alibis. You’ll need to walk the fine line between professional and friendly, keep a cool head when you’re hearing the horrors, and be able to put together everything you’ve learned in a well written report – best get the coffee ready.

Translations: I've included the English Strings in the file; if anyone is talented enough to translate, I would be incredibly grateful, so please let me know in the comments!

With thanks: To MissyHissy's career building tutorial!

[companysconnectsin]

CSV Certification

Gain expertise in Pharmacovigilance with our comprehensive CSV Certification. Learn regulatory compliance, adverse event reporting, and signal detection. Enhance your career in drug safety and surveillance. Earn a recognized certificate for your skills.

Get more details at: www.companysconnects.com/computerized-system-validation

[igmpi]

Post Graduate Diploma/Executive Diploma in Clinical Research Describtion- Our Clinical Research program provides the knowledge and skills necessary to design, conduct, and analyze clinical research studies

[problogsposts]

Balancing Benefit and Risk in Clinical Research

Introduction

The fields of medicine and healthcare are rapidly developing. Companies and research institutes play a vital role in advancing medical knowledge through clinical research. Clinical research surrounds various aspects, including medical coding, pharmacovigilance, drug regulatory affairs, and clinical data management. These fields are essential in ensuring the safety and effectiveness of new medical treatments. However, conducting clinical research comes with its own set of challenges, particularly when it comes to balancing the benefits and risks involved.

The Role of Clinical Research

Clinical research is the backbone of medical progress. It involves the systematic study of new drugs, medical devices, treatments, and procedures to determine their safety and efficacy. Companies and research institutes conduct clinical trials to gather data and evidence before these medical interventions are approved for widespread use.

Key Areas of Clinical Research

1. Medical Coding: Medical coding is like the language of healthcare. It involves translating medical records, diagnoses, and procedures into standardized codes. Accurate coding is crucial for proper billing and maintaining patient records.

2. Pharmacovigilance: This field focuses on monitoring the safety of drugs and vaccines post-approval. It helps identify and prevent adverse effects and ensures that patients receive safe medications.

3. Drug Regulatory Affairs: Drug regulatory affairs professionals work with regulatory agencies to ensure that new drugs meet safety and efficacy standards before they reach the market. They help companies navigate complex regulations.

4. Clinical Data Management: Managing clinical trial data is essential for maintaining the integrity of research. Data managers organize and validate information collected during trials.

Balancing Benefit and Risk

While clinical research is definitely important for medical progress, it also involves risks. Here are some ways in which companies and research institutes can strike a balance:

1. Ethical Considerations: Ethical guidelines and standards are the foundation of clinical research. Researchers must prioritize the well-being of participants and ensure that their rights and privacy are protected.

2. Informed Consent: Participants must provide informed consent before participating in a clinical trial. They should be fully aware of the potential risks and benefits, enabling them to make an informed decision.

3. Safety Monitoring: Continuous monitoring of participants' safety is essential. Any adverse events should be immediately reported and addressed.

4. Transparency: Transparency in reporting research findings is crucial. This includes disclosing both positive and negative results, helping to avoid biased information.

5. Regulatory Compliance: Companies and institutes must adhere to regulatory requirements in their respective fields, ensuring that the research meets high standards of safety and quality.

The Importance of Training

To ensure that clinical research is conducted responsibly, professionals in the field require acceptable training. Courses and training programs are available for medical coding, pharmacovigilance, drug regulatory affairs, and clinical data management. Proper training equips individuals with the knowledge and skills needed to conduct research while minimizing risks.

Job Placement in Clinical Research

For those interested in pursuing a career in clinical research, the job placement aspect is essential. Companies and institutes often offer placement opportunities for trained professionals, ensuring that they can apply their skills in real-world settings.

Conclusion

Balancing benefit and risk in clinical research is a complex but essential endeavor. Companies and research institutes play a critical role in advancing medical knowledge, but they must do so responsibly. Ethical considerations, informed consent, safety monitoring, transparency, and regulatory compliance are key factors in achieving this balance. Moreover, individuals interested in clinical research can benefit from training and job placement opportunities, enabling them to contribute to the field while ensuring the safety and well-being of patients. In this way, we can continue to make significant strides in healthcare while upholding the highest standards of ethics and safety.

[gayf1hoe]

Behind the Pit Wall

Scenario - Y/N is a new race engineer for Williams but he never expected to become a race engineer straight away, bit following the resignation of Logan's race engineer he receives a very prompt promotion. The two quickly hit it off professionally but their relationship quickly exceeds professional.

Race 1 - Spa 

Nervously and full of anticipation I take my seat on the pit wall for the first time as a race engineer for Williams.

Ever since graduating University I have been working in F1 for the past 2 years, last year I was with Sauber as a junior race engineer and I applied to Williams on the off chance they would actually agree to take me but to my genuine surprise they did. 

When I first met with James he said I would be a secondary Engineer in other words I was just there to assist the main engineer. However when I walked in this morning I was told I would be Logan Sargeant's permanent race engineer after his engineer resigned unexpectedly. 

As I'm sitting in the pit wall looking at all the data, it's starting to set in. I'm a driver's race engineer with just a year's experience, talk about being thrown in the deep end. 

Logan hasn't got the best track record but he's a great person with a great sense of humour and undeniable charm so I am honoured I get to work with him. 

After qualifying yesterday we are in P11 and we missed out on Q3 by 0.012 so it's a little frustrating but the way things go in F1. 

“Logan radio check” 

“Yep, your voice sounds great, and mine” 

“even better, 30 seconds to lights out maintain focus and be clinical” 

When the lights go out my heart pounds faster and my palms sweat a little. 

We don't have the best start as Logan ends up in P15 and with the weather conditions around Spa showing no signs of improving cars are spinning left, right and centre. The strategists and I decide to bring Logan in now for the inters before everyone else 

“Logan box, box” 

As he comes in I see a train of cars following behind him but our crew do a fantastic job at fitting the new tyres that will stay on until the chequered flag.

Logan emerges back on the track at P11 which is a great advantage for us and I coach him through every lap telling him where he can improve and with that he manages to overtake a few people, and by the final lap he's probably sick of my voice. 

“Logan that's P7 really good job today, do your cool down lap and we will see you in Parc Fermé”

“Yeah good job, thanks for all your guidance today we did great today, we will continue to improve”. 

“Absolutely, sorry if my voice became annoying”

“Never I loved hearing your voice every second, and that's not sarcasm”. 

After the race I am interviewed by a reporter about what I think of my first race as a lead race engineer.

Reporter: Y/N great result for your first race. How did it feel to be thrown right in at the deep end and get such a great result?

Y/N: Yeah of course it was stressful being thrown in at the deep end, I arrived in the paddock this morning and was told I'm Logan's new race engineer so it was a little stressful but we did really well despite the conditions and it's a good start for Logan.

Reporter: We saw you too having lets say some ‘flirtatious moment's’ . Is there a relationship brewing?

Y/N: Haha me and Logan are just naturally flirtatious people and I think we have a good work relationship together.

As I'm answering questions Logan comes from behind me and jump scares me and the reporter turns her attention to him.

Reporter: Logan what do you think of your new race engineer?

Logan:  He's amazing and he really helped me out there today so I'm grateful I have got him

Reporter: You complimented his voice a few times, is there something going on there? 

Logan: Well yes he has a naturally calming voice and it's great to hear in stressful situations. 

Race 24 - Abu Dhabi 

As my second season in F1 comes to an end I am extremely happy where Logan is at P8 in the championship with only 1 point separating him and Stroll. 

Coming into this season we could never have predicted that me or him would do this well this season and since Logan has been performing so well this season consistently he is on the move to Mercedes next year but what he doesn't know is that I am also moving to Mercedes. 

Additionally since the season exposition mine and Logan's relationship has well let's say developed. It is sort of unconfirmed knowledge that we are dating but neither of us confirmed it but our constant flirting and physical contact has confirmed it for us.

“Logan 30 seconds to lights out I want a great finish from you today” 

Logan starts from P6 which is his best starting position in his career so I'm anticipating a good race. 

He gets a good start and quickly takes P5 from Norris and maintains a good pace. 

When he comes in for his first and only pit of the race and he drops down to P10, one of Logan's biggest problems is that after a pit stop and he loses positions he thinks it's all over so we have been working on his

resilience and as he was the first car to pit I know that the cars in front will pit soon and he will be bumped up a few places. 

With 15 laps to go Logan has made his way up to P5 and is chasing Lance for P4 and heading along the DRS straight he manages to get past and we now set our eyes on Oscar Piastri.

“Alright Logan it's Piastri ahead 2.1 seconds they are having mechanical issues with their brakes” 

For 14 laps straight Logan is tailing Oscar and it's painful and nerve wracking to watch but in the final lap in the final DRS zone Logan squeezes past him and whilst it's a good move the team doesn't celebrate just yet. But when he crosses the line there is a roar of cheers from the garage behind me.

And my normal angelic radio voice turns into a coarse shout 

“Logan that is P3, well done, I'm so proud of you and the improvements you have made and those 15 points put you in P6 in the standings”

“Y/N thank you for all your hardwork and dedication this year you have really helped me achieve great things and I will really miss hearing your voice”

“Well, do you want another piece of good news?” 

“Of course” 

“You aren't going to Mercedes alone, I'm coming along as well as your race engineer” 

“Holy shit that's the best thing I have been told, I would have missed your voice on the radio. I love you Y/N”

“I love you to Logan”

For the first time Logan is on the podium and the entire team is here watching him and cheering him on. 

It's a great sight to see him smiling and finally believing in himself.