Medical Research Jobs
Medical research jobs provide individuals with the opportunity to make significant contributions to the advancement of medicine and healthcare. These positions involve conducting clinical trials, laboratory research, and analyzing data in order to develop new treatments for diseases. Working in medical research requires a high level of scientific knowledge, analytical skills, and critical thinking. Professionals in this field often collaborate with other researchers from different disciplines to conduct studies that aim to improve patient care and treatment options. Medical researchers also work closely with doctors, nurses, and other healthcare professionals so they can share their findings and better understand patient needs. With such a wide range of responsibilities, medical researchers play an essential role in driving innovation in the medical industry. The advancement of modern medicine is dependent on the insights that these professionals provide through their investigations. As such, medical research jobs offer ambitious individuals the chance to make a meaningful contribution to humanity’s ever-evolving knowledge of health and well-being.
Clinical Research Associate (CRA): Designs and implements clinical trials according to established protocols. Monitors the progress of trials and reports results to principal investigators. Salary range from $50,000 to $90,000 per year. CRA Certification through CCRPS requires completion of a 8-week course on research principles and methodology plus two years of experience in clinical research related activities such as site monitoring or data management.
Clinical Research Coordinator: This position involves coordinating the clinical aspects of research studies, such as collecting and organizing data, tracking recruitment of study participants, managing patient information, and monitoring research protocols. Salary range: $43,000 to $55,000 per year. Get CRC Certification through CCRPS: Certified Clinical Research Professional (CCRP).
Clinical Trials Manager (CTM): A Clinical Trials Manager is responsible for overseeing the entire clinical trial process from start to finish. They ensure the compliance of all study protocols while managing timelines and budgets. Salary range: $70,000-$90,000 per year; Certification through CCRPS: Certified Clinical Trial Manager (CCTM).
Medical Research Lab Technician: Responsible for performing laboratory tests according to established protocols in order to aid in medical research projects. Salary range: $35,000 to $45,000 per year. Certification through CCRPS: Certified Laboratory Technician (CLT).
Bioinformatics Scientist: Utilizes computer technology and statistical analysis in order to analyze biological data derived from experiments in medical research labs. Salary range: $75,000 to $100,000 per year Certification through CCRPS: Certified Bioinformatics Scientist (CBS).
Medical Writer: Writes and edits materials for clinical trials and other medical research projects, including study protocols and reports for publication or regulatory submission purposes. Salary range: $60,000 to $80,000 per year Certification through CCRPS: Certified Medical Writer (CMW).
Regulatory Affairs Manager: Manages the regulatory affairs process by ensuring that medical products adhere to applicable regulations throughout their development and commercialization phases. Salary range: $95,000 to $125,000 per year Certification through CCRPS for Certified Regulatory Affairs Manager (CARM)
Regulatory Affairs Specialist: Develops regulatory strategies for the submission of clinical trial applications to regulatory agencies, monitors global regulations governing clinical trial design and implementation and tracks changes in legislation affecting the development process of drugs, biologics or medical devices; coordinates communication between sponsors, investigators and regulatory authorities; prepares high-quality documents such as study protocols and amendments for submissions to regulatory bodies; participates in meetings with regulatory agencies worldwide; performs literature searches related to drug development topics; assists with ongoing maintenance of regulatory files as required by regulations. Salary range from $55,000 to $100,000 per year depending on experience level. Pharmacovigilance Certification through CCRPS requires completion of a 8-week course on research principles and methodology plus five years minimum experience in pharmaceutical industry or related fields with emphasis on Regulatory Affairs functions.
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Putting fictional characters into colony building games is fun.
I just put the ninja turtles into Rimword and, as of barely a month in game, Mikey was kidnapped and converted to an enemy clan, Raph has a fking army of 20+ chickens, and Leo almost had a mental breakdown because i didn't give him a hat. Donnie, oddly enough, has caused me no issues and is doing everything perfectly.
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(Raises hand)
What is age regression a thing you’re diagnosed with or is it self diagnosed? Sry I just would like to know more and I’m confused on how you would know you are age regressing as well. Just wanna know for future reference :)
I'm not a doctor, and I haven't been diagnosed bc a lack of resources (we love capitalism /s), but it's either-or, honestly. Having a proper diagnosis could help with understanding it, but in my personal experience, it's not necessary to know that you do it.
Age regression is a real and recognized symptom of things like PTSD. You just have to do the proper research and learn to recognize when it happens.
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if I had a nickel for every time someone came to their appointment with an untreated, dangerous, highly contagious disease and lied to us about it, saying they don’t have it, until after we’d done their whole visit and drawn their blood, I’d have two nickels. Which isn’t a lot. But it’s fucking diabolical that it’s happened twice
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First day in a new job.
I am now starting the antibiotic research using bacteria from an actual hospital! How exciting is that!!
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Should learn whether or not I got the vet tech position this week, so if ya see a bunch of personal posts about feeling like I’m underachieving and wasting my life and wondering what the fuck I’m doing then you know why!!! ✌️🙃👍
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things that i've been told in the process of accommodations ***before my first appointment*** (all the things in quotations are direct quotes)
you need to provide documentation to have an interpreter at the accommodations meeting.
(a couple days later) lol jk talked to my boss and that's ILLEGAL hahaha. sorry not sorry for giving you a breakdown (both of these were also from my boss bc i Work in the disability office).
(different coordinator who isn't also my boss, as i'm sobbing at work and said "why do these things always have to be a fight?") "it's not a fight, this is just the process everyone goes through."
me, to my boss: the process of getting accommodations is pretty invasive. my boss: "it's not invasive!" you just need to "provide enough of a narrative" so we understand how everything affects you. "we need to be able to determine what you need."
me, internally screaming that i am literally telling you what i need and my doctor + therapist are backing me up! just not with enough invasive detail for you to be satisfied.
my boss' boss, who handles deaf students, when i asked specifically what documentation i need: well, every case is different, and actually i recommend not bringing any documentation to the first meeting.
the way the accommodations system works is either you bring in enough documentation for your first appointment and get accommodations approved then, or you have to wait weeks to a month or more to get a second appointment when you do have documentation to have that reviewed and see if it's enough. if it's not, rinse and repeat.
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