Clinical research is all about studying people to figure out what causes, treats, and prevents diseases. It's a crucial part of developing new therapies and medication by pharmaceutical companies.  Researchers conduct carefully planned studies to get reliable and scientifically sound infomation to determine the safety and effectiveness of the experimential medicines. 

Yes, the CRO internship is fully remote and designed to fit seamlessly into your work or school schedule. It’s a flexible and convenient opportunity, typically lasting 4 weeks. The expertise you gain is equivalent to that of someone with one year of experience. Plus, we’re the only program in the industry offering this unique bridge program, which provides valuable hands-on experience.

Comparable programs cost between $9,000 and $12,000, but we charge only a fraction of this amount. What are you waiting for? We’ve created the best and most affordable program, and you get to reap the benefits!

YES. Following our recent overhaul of our program, Obedtek is revolutionizing the industry with a pioneering bridge inetrnship program that is the first of its kind.

It offers hands-on experience, so by the time you’re finished, you’ll feel as though you’ve been in the industry for a year—and you’ll receive an employment recommendation letter reflecting that level of expertise.

Our programs are designed to ensure financial accessibility, removing barriers for those pursuing a career in clinical research. Through our partnership with Afterpay, we offer flexible payment plans with options for up to 6 or 12 monthly installments, starting at just $300 per month.

Yes, seats are limited. We accept a select number of candidates per cohort, so if you miss one, you will need to wait for the next round.

The Obedtek Clinical Research program, featuring a unique internship bridge, accelerates your entry into essential clinical research roles. Upon completion, you'll gain experience equivalent to one year on the job, despite the program's shorter duration. The training and internship experience distinguishes you from other applicants vying for the same position, making it a priceless investment in your career. Without it, entering the industry could be a daunting task.

Clinical Research Associates play a key role in monitoring and managing clinical trials. They ensure that the study is conducted in compliance with protocols, regulations, and good clinical practices. CRAs often visit clinical trial sites, review data, and maintain communication between the sponsor and investigators.

Clinical Research Assistants support the overall research process. They may assist in recruiting participants, organizing study documentation, and coordinating logistics. Their responsibilities vary, but they generally provide crucial administrative and operational support to the research team.

Clinical Research Coordinators are responsible for managing the daily operations of clinical trials. They liaise between the sponsor, investigators, and study participants. CRCs oversee protocol adherence, maintain regulatory compliance, and handle data collection. They also ensure that the study runs smoothly and efficiently.

Clinical Research Associates primarily op

erate remotely from home, with occasional travel to research centers as needed. On average, a CRA undertakes approximately 4-6 onsite visits per month. However, there are CRA roles that are office-based.  

The work arrangement for Clinical Research Assistants varies based on the company's structure, allowing for both remote and onsite positions.

Clinical Research Coordinators typically hold office-based roles and are not generally involved in remote work.

There are many more positions that we place for that include either remote, hybrid or in-person working arrangement:

• Clinical Data Analyst

• Clinical Patient Coordinator

• Clinical Trial Manager 

• Clinical Systems Coordinator

• Clinical Trial Associate

• TMF Associate

• Data Manager

• Drug Safety Associate

We offer scholarship awards every month. Inquire with your career coach on how you can apply. 

Typically, if accepted, the remote internship will start 3-5 days after you successfully complete the online program. If we are unable to secure a placement for you, you will receive a full refund.

Clinical Research Coordinator (CRC):

Entry-Level: $50,000 - $60,000 per year

Mid-Level: $60,000 - $80,000 per year

Senior-Level: $80,000 - $100,000+ per year

Clinical Research Associate (CRA):

Entry-Level: $75,000 - $10,000 per year

Mid-Level: $110,000 - $130,000per year

Senior-Level: $140,000 - $170,000+ per year

Clinical Research Manager:

Mid-Level: $80,000 - $100,000 per year

Senior-Level: $100,000 - $130,000+ per year

Clinical Research Director:

Senior-Level: $120,000 - $160,000+ per year

Clinical Trial Investigator:

Varies significantly: $100,000 - $300,000+ per year

Clinical Research Scientist:

Entry-Level: $70,000 - $90,000 per year

Mid-Level: $90,000 - $120,000 per year

Senior-Level: $120,000 - $150,000+ per year

Drug Safety Associate:

Entry-Level: $50,000 - $65,000 per year

Mid-Level: $65,000 - $85,000 per year

Senior-Level: $85,000 - $105,000+ per year

Drug Safety Specialist:

Entry-Level: $55,000 - $70,000 per year

Mid-Level: $70,000 - $90,000 per year

Senior-Level: $90,000 - $120,000+ per year

Pharmacovigilance Specialist:

Entry-Level: $55,000 - $70,000 per year

Mid-Level: $70,000 - $95,000 per year

Senior-Level: $95,000 - $130,000+ per year

Drug Safety Manager:

Mid-Level: $85,000 - $110,000 per year

Senior-Level: $110,000 - $150,000+ per year

Clinical Trial Specialist:

Entry-Level: $55,000 - $70,000 per year

Mid-Level: $70,000 - $90,000 per year

Senior-Level: $90,000 - $120,000+ per year

Clinical Data Manager:

Entry-Level: $60,000 - $75,000 per year

Mid-Level: $75,000 - $95,000 per year

Senior-Level: $95,000 - $130,000+ per year

These salary ranges provide a general idea and may vary depending on factors such as company size, geographic location, and individual qualifications.