What We Do

At BioBridges, our dedicated and experienced staff of clinical experts manage all aspects of clinical trials for life sciences, pharmaceutical companies, biotech companies and medical device companies. We understand it doesn't always make sense to have the necessary resources in-house on a full-time basis. And that's where we come in. Our highly skilled medical consultants serve as an integral part of your team, helping researchers bring innovative products to market efficiently and safely.

Our model enables you to engage exceptional life science consultants, as needed,
who are focused on your work and provide the skills and experiences you require.

Clients

Experience that works.

We know that you have real work that needs to be accomplished. We also know that it can only be realized if you have access to highly skilled and experienced medical consultants in a flexible and managed manner that aligns with your immediate program needs.

Over the years, BioBridges has successfully supported hundreds of programs for emerging and established pharmaceutical companies, biotech companies, and medical device companies. Our clients recognize the correlation between the ability to accomplish the work and their success in advancing science and producing therapies for patients who need them. And helping our clients expose the world to beneficial therapies that can truly make a difference is something we too, are very passionate about.

The BioBridges Approach

BioBridges serves as an integrated extension of your programs; engaging high-impact professionals as individuals, project teams, and functional teams in a fluid manner that is scalable, flexible, and specific to your programs' objectives. We are committed to accomplishing the work that allows you to achieve both your short- and long-term development goals.

Process

Our process ensures that we successfully scope, support, and accomplish the work at hand for each client

Collaboration

When you work with BioBridges, you become part of a collaborative and thorough approach that is focused on serving your needs

Dedication

With both a client services representative and a functional expert, your team has the experience and first-hand knowledge necessary to engage professionals who can achieve your specific program objectives

Frequently Asked Questions

Do you guarantee constant work?

While we don't guarantee continuous work, BioBridges has been in the emerging market biotech space for more than 17 years and have worked with over 600 biotech companies, as well as medical device, and large pharma project teams during that time. Many of our Clinical Development professionals enjoy a variety of work presented and that hopefully inspires.

What types of clients do you have?

We have worked with over 600 biotech companies, as well as medical device, and large pharma companies

Does your company offer permanent employment at your clients?

While we don't seek to make permanent placements as a part of our service deliver model, on occasion, some of our professionals choose to convert to permanent employment with our clients, according to the terms of the contracts we have in place with our clients.

What are the average number of years of Clinical Development experience among your internal staff?

Our secret sauce is our Functional Expert model. They are a part of our leadership team and provide advice to our Career Manager and Client Services staff in determining skills and fit with our professionals and our clients.

Do you have ongoing training for your internal staff?

Yes, we have periodic “Lunch & Learn” venues and attend key professional education and association meetings.

Do you offer benefits to your consultants?

Yes, many of our Clinical Development professionals are W2 employees of ours and are offered a robust and competitive benefits package.

How often will I be paid as an employed consultant of BioBridges?

We pay our employee professionals on a weekly basis.

Do you require your consultants to sign contracts?

We have an onboarding packet inclusive of contracts for both our W2 employed staff as well as our independent contractors.

Service Areas

Biostatistics

Biostatistics is responsible for the development of statistical analysis plans for clinical studies and proper interpretation of scientific data generated from clinical studies.

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Clinical Operations

Clinical Operations, or Clinical Trial Development, is responsible for the management and oversight of clinical studies with direct oversite of vendors, clinical sites, and clinical research organizations (CROs).

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Data Management

Clinical Data Management (CDM) is a critical aspect of clinical research, which leads to the generation of high-quality, reliable, and statistically sound data from clinical trials.

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Medical Affairs

Medical Affairs is responsible for developing, managing, and optimizing the lifecycle of a product after it has been approved.

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Medical Oversight

Medical directors are key to drug development teams and are responsible for clinical program leadership, clinical study development, oversight, monitoring, and reporting. This function can have input into initial study design, protocol, development, full study execution, or select medical task assistance.

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Non-Clinical

Non-clinical is responsible for estimating and optimizing the safe dose for the first-in-human study and predicting a product's safety profile.

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Program Management

Program Management is responsible for advancing an experimental product across functions, from research to development to commercialization.

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Quality Assurance

Quality Assurance assures that products have appropriate characteristics of “safety, identity, strength, quality, and purity.”

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Regulatory Affairs

Our Regulatory Affairs consultants ensure that your company complies with relevant regulations and laws, liaises with regulatory agencies (such as FDA) and internal teams on specific issues pertaining to drug/device development, and leads cross-functional teams to develop regulatory submissions (IND, NDA, etc.)

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Safety & Pharmacovigilance

Drug safety, also known as pharmacovigilance (PV), is the pharmacological science relating to the collection, detection, assessment, monitoring, and prevention of adverse effects with pharmaceutical or device products.

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Functional Expertise

BioBridges' functional experts work with you to assess and understand your programs and best leverage our consultants' career portfolios® to your benefit.

Whether you need highly specific individual skills, CRO oversight, or functional teams, our functional experts have extensive knowledge, experience, and a wide range of expertise. From Biostatistics and Clinical Operations to Medical Oversight and Regulatory Affairs, our specialists will help you successfully accomplish the work at hand.

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Meet our functional experts.

William Heydon

| BioBridges Professional
Over the past few years, I have been contacted by an number of agencies regarding projects. Most turn out to be “black holes” where I submit a resume and never hear anything back. BioBridges has reached out to me with a number of opportunities. I am now working with a gene editing company who plans to file their first IND later this year. I appreciate all of the attention and guidance I receive from BioBridges, and highly recommend them.

Ariel Brown

| BioBridges Professional
My work with BioBridges has been one of a kind. I have worked with several consulting companies and this one has been the best! They are extremely efficient and make sure their clients are well taken care of. I worked closely with Lygia who has provided so much help during the process of working with a new company. From interview/company prep to occasional check-ins to making sure you're happy with your current assignment.

Crystal Little

| BioBridges Professional
What do I like most about working at Biobridges is 1) the people I work with, and 2) the freedom to create a way of working that works best for me.

Biobridges hires THE BEST people, and I've always found it easy to fit in, and learn the business. It's a company that offers you diverse professional experience.

Jeaneen Wallis

| BioBridges Professional
So working with BioBridges has been a big improvement from my previous staffing organization. The people are available (...even on their way to the gym) and readily share information about new opportunities. I feel engaged and not left alone once the contracts are signed. They were also supportive in making recommendations when I needed to change my business insurance.

Jerilyn Jacobson-Russo

| BioBridges Professional
Being part of Biobridges is like being part of a family. I have worked with the team for almost twenty years now. They have helped me procure employment after my son's birth, a death in the family, and several layoffs. They have celebrated my marriage and various accomplishments with their client.

I value the care they show to ensure my placement is a good fit for all involved, and they always advocate in my best interest. I am grateful that they are both employers and friends of our family.

Afrooz Afghani

| BioBridges Professional
There are so many factors that make BioBridges a special place to work for. First and foremost, is the fact that you have someone (your 'career manager') who goes to bat for you. Finding the right position is really a full-time job and the career manager takes over that responsibility and gives you full support throughout the process. Secondly, BioBridges makes sure you don't set yourself up for failure when it comes to CV preparation, career summary details, and submitting you for the most suitable jobs. And last but not least, I love the fact that you have the opportunity to work for several different clients with various needs, unique therapeutic areas, and exceptional professionals. In short, BioBridges offers the best work scenario for busy individuals who want flexibility and independence in their careers. I love it!

Shari Thomas

| BioBridges Professional
BioBridges is the best company I've ever worked with and I always recommend them to my network.

I've been with BioBridges for five year and have always been placed with high performing clients. Each client has told me they choose BioBridges for talented, skilled, and qualified candidates for their company's business needs. I'm proud to work for BioBridges, and even prouder to know industry's clients recognize our value in contributing to their success.

Julie Crider, PhD

| BioBridges Professional
I really appreciate the time and effort the Biobridges team takes to ensure that my skills are a good fit for each upcoming project. There is always 'someone in my corner' when I take on a new project. Regular check-ins with my career director serve to provide updates on projects. A team member gives me feedback from the client so that I can make sure my work is 'on target'. Finally, the invoicing process is very convenient and the promptness of payment is exceptional. Overall, I'm very pleased with my collaboration with the BioBridges team and highly recommended them to potential contractors as well as companies seeking well-qualified clinical development professionals.

Christopher M. Cameron , PhD

| BioBridges Professional
I have been a medical writing consultant for nearly 10 years, 3 of it with Biobridges. I have found them to be extremely responsive, professional, and a great pleasure to work with. They have provided me with a constant stream of interesting, stimulating work for a variety of clients. Unlike some vendors, they are extremely sensitive to the amount of work that they send my way - cognizant both of the fact that it could be too much or too little, depending on the writer.

Their rates are quite favorable and they pay promptly every Friday.

I hope our professional relationship continues until my retirement.

Ready to begin?

Let's talk about how our clinical experts can help your clinical trial run as efficiently and effectively as possible.

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