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Bioclinica Research Jobs (NOW HIRING)

Bioclinica

Pricing & Proposals Analyst

Princeton, NJ · On-site

Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device ...

Bioclinica

HRIS Analyst (Workday)

Princeton, NJ · On-site

Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device ...

Bioclinica

Clinical Project Manager

Princeton, NJ · On-site

Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device ...

Bioclinica

Clinical Project Manager

Franklin, TN · On-site

Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device ...

Bioclinica

Associate Medical Writer

Princeton, NJ · On-site

Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device ...

Bioclinica

Head of R&D, AI Integrations

As we continue to scale, we are seeking a Head of Research & Development to lead the evolution of our global technology organization. This role serves as a key technical and organizational leader ...

Integrated Resources INC

MRI Technologist

Newark, CA

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. The candidates ... and BioClinica operations personnel Representing the radiology services group in project team ...

Collabera

Clinical Project Manager

Santa Clara, CA

Partner with global Clinical Research functions to identify business needs and propose new/enhance ... Medidata CTMS, BioClinica CTMS, ArisGlobal CTMS) 3) eTMF Solutions (i.e. VEEVA, Documentum ...

Bioclinica

Sr Cardiologist

$362K - $409K/yr

Ongoing professional development and research engagement What You'll Be Doing * Represent Clario by providing cardiology expertise to pharmaceutical sponsors across consulting services, including ...

Bioclinica

Director, Cardiac Solutions

Experience within clinical research, diagnostics, life sciences, pharmaceutical, biotechnology, or CRO environments. * Proven success in major account management and consultative selling within ...

Bioclinica

Medical & Scientific Affairs Advisor

... research, helping bring lifechanging therapies to patients faster. What We Offer * Competitive compensation * Comprehensive health, dental, and vision coverage * Retirement savings plan with company ...

Bioclinica

Read Services Specialist

Experience working in a regulated environment such as clinical research, healthcare, pharmaceutical, or medical imaging preferred. * Strong proficiency in Microsoft Excel, including data ...

Bioclinica

PET Scientist

Our scientific, imaging, and technology teams support global clinical trials in highly regulated environments, delivering highquality imaging endpoints that advance neuroscience research. In this ...

Bioclinica

Solutions Design Analyst

Familiarity with FDA regulatory processes and clinical research standards. * Highly organized, self-directed, and comfortable managing multiple projects in a fast-paced environment. * Excellent ...

Bioclinica

Lead Project Manager

As a Lead Project Manager, you will play a critical role in leading project teams, managing client relationships, and ensuring the successful delivery of clinical research programs. If you are a ...

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How much do bioclinica research jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for bioclinica research in the United States is $35.45, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $44.23 per hour, depending on experience, location, and employer.

What is Bioclinica Research?

Bioclinica Research is a contract research organization (CRO) that specializes in providing clinical trial services to pharmaceutical, biotechnology, and medical device companies. They support the development and approval of new drugs and medical devices by managing and conducting clinical trials, collecting and analyzing data, and ensuring regulatory compliance. Their work helps bring new therapies to market safely and efficiently.

How does a professional in Bioclinica Research typically collaborate with cross-functional teams during a clinical trial project?

Professionals at Bioclinica Research frequently work alongside cross-functional teams, including clinical operations, data management, regulatory affairs, and biostatistics. Effective collaboration involves regular meetings to ensure protocol compliance, timely data collection, and issue resolution throughout the trial lifecycle. By working closely with diverse teams, Bioclinica staff help streamline workflows, maintain high-quality standards, and adapt quickly to evolving project needs. This collaborative environment fosters professional growth and offers exposure to a broad spectrum of clinical research activities.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate at Bioclinica, and why are they important?

To thrive as a Clinical Research Associate at Bioclinica, you need a background in life sciences, clinical research experience, and often a relevant degree such as a BSc or MSc. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and regulatory certifications like GCP (Good Clinical Practice) are typically required. Strong attention to detail, organization, and effective communication make a candidate stand out in this role. These skills are crucial to ensure compliance, data integrity, and successful coordination of clinical trials within strict regulatory environments.

What is the difference between Bioclinica Research vs Clinical Research Coordinator?

AspectBioclinica ResearchClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonUsually requires a bachelor's degree; certifications like CCRP or CRC are advantageous
Work EnvironmentWorks in clinical trial settings, often at research sites or pharmaceutical companiesWorks at research sites, hospitals, or clinics managing trial activities
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research clinics, pharmaceutical companies

Bioclinica Research professionals focus on managing and supporting clinical trials, often within CROs or biotech firms, while Clinical Research Coordinators primarily oversee trial activities at research sites. Both roles require similar credentials and work in clinical environments, but their specific responsibilities and employer settings differ slightly.

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What job categories do people searching Bioclinica Research jobs look for?

The top searched job categories for Bioclinica Research jobs are:

Bioclinica Research jobs near you
Infographic showing various Bioclinica Research job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 10% Part Time, and 1% Contract. Highlights an 78% Physical, 4% Hybrid, and 18% Remote job distribution, with an average salary of $73,741 per year, or $35.5 per hour.

Pricing & Proposals Analyst

Princeton, NJ • On-site

Bioclinica
1 - 5K employees
Learn more about Bioclinicaexternal

Full-time

Re-posted 4 days ago

Job description

Company Description
Bioclinica is one of the leading global CRO company which focuses on bringing efficiency to the clinical trials. We have a premier global research network-and the only one with investigator sites in the U.S., Europe, Latin America, and Asia. We are headquartered in Doylestown, PA. Bioclinica offers a network of research sites, patient recruitment-retention services, and a post-approval research division. We serve more than 400 pharmaceutical, biotechnology, and device organizations
Job Description
Primary Responsibilities
Generates, analyzes, and manages accurate and timely client proposals by:
  • Reading, analyzing, and collaboratively working with the functional team owners to understand client's Request for Proposal ("RFP") & protocol. Ensuring value add pricing where appropriate.
  • Reading, analyzing, and collaboratively working with project managers and functional team owners to ensure accuracy and completeness of change orders requests and to create change order budgets and coordinate generation of additional scope of work language when required.
  • Reading, analyzing, and collaboratively working with the functional team owners to understand client's Request for Information ("RFI") and ensuring RFI answers are maintained the RFI library. Determining standard, variable, and value add costing parameters based on RFP and protocol.
  • Contributing to standard, variable, and value add costing parameters based on RFP and protocol.
  • Coordinating & collaborating with team members to review Fee Schedules for large trials and/or Programs to determine best pricing strategy and provide guidance and approval, while keeping GS, BU Heads, SMEs and Sales updated throughout the process.
  • Incorporating any required sponsor revisions into cost formulas and documenting same for all proposals or change orders generated within the proposals group.
  • Discussing and Reviewing all proposals per current Bain RAPID approval matrix
  • Ensure Pricing generated within the proposals group meetings margin guidelines per the approved gross margin calculator or PriceBook

Ensures pricing and proposals timelines are met by:
  • Managing workload and ETA's for assigned requests
  • Attending and preparing information for team meetings

Maintains Quality Service and Departmental Standards by:
  • Ensuring ongoing understanding of Bioclinica services
  • Reading, understanding and adhering to organizational Standard Operating Procedures (SOPs)
  • Assisting in establishing and enforcing departmental standards
  • Ensuring all reviews, approvals, documents and analysis are filed in accordance to team requirements.

Secondary Responsibilities
Contributes to team effort by:
  • Exploring new opportunities to add value to organization and departmental processes
  • Helping others to accomplish results
  • Performing other duties as assigned and deemed necessary

Qualifications
Education:
  • Bachelor's degree required

Experience:
  • 2+ years relevant experience in a pharmaceutical or CRO environment required
  • 1+ years contracts/proposals experience required
  • Knowledge of basic legal concepts and experience drafting and negotiating contracts required
  • Knowledge of medical and pharmaceutical industry, terminology and practices preferred
  • Intermediate to Expert in Microsoft Office applications including Excel, Word and Access required
  • Previous experience in a clinical imaging environment and/or clinical trials experience within a CRO or pharmaceutical research organization preferred

Additional skill set:
  • Ability to work independently or in team setting; ability to adjust to changing priorities
  • Excellent attention and orientation toward meticulous work
  • Strong organization skills and ability to prioritize and meet deadlines
  • Strong interpersonal and communication skills, both verbal and written
  • Ability to project and maintain a professional and positive attitude

Additional Information
Working conditions:
  • Travel: 0-20%
  • Lifting: 0-15lbs
  • Other: Computer work for long periods of time

EEO Statement
Bioclinica is an equal opportunity employer. Bioclinica evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic

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