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Whether you are healthy, or have a specific illness, we'll connect you with the right trial. Potentially get paid to access the most cutting edge medicines combating your disease. Most trials don't require much effort and will be located near you.

Proficient scientific expertise to propose, design, and execute clinical research and development studies, and authors documents related to clinical trials, such as medical monitoring plan, SAPs, informed consent and clinical components of the Clinical Study Reports. As a Senior Clinical Scientis...

Clinical Scientist that will serve as a key role contributing to the scientific planning and collaborate with both Clinical Research, Pharmacovigilance and Clinical Operations in the execution of multiple global clinical trials. Proficient scientific expertise to propose, design, and execute clin...

We are seeking a seasoned physician with a strong clinical background and a passion for drug development to join our Clinical Development team to serve as a Study Responsible Physician as an Executive Director, Clinical Research. ...

Senior Clinical Supplies Management Specialist. Develops and implements the initial timeline, budget, drug supply forecasts, and component requirements needed for preparation of the Clinical Supply Master Plan for Phase I through IV clinical protocols. Reviews Clinical Research Development progra...

Proficient scientific expertise to propose, design, and execute clinical research and development studies, and authors documents related to clinical trials, such as medical monitoring plan, SAPs, informed consent and clinical components of the Clinical Study Reports. As a Senior Clinical Scientis...

Thank you for your interest in becoming a Paid Product Tester. This opportunity is for completing market research opportunities with independent brands via online or phone. Online studies typically take 15 minutes, while telephone interviews may take 30-60 minutes each session. Compensation varie...

TCS Intelligent Life Sciences Operations (Pharma, MedTech, Clinical Research Operations) is part of the TCS Life Sciences business unit, delivering business operations for Pharma, MedTech and Contract Research Organizations (CROs). TCS Life Sciences delivers to our customers strategic goals and o...

Requirements Medical license (MD, DO) - New Jersey 2 years experience as a Clinical Research Investigator (Principal Investigator or Sub-Investigator) Bilingual Spanish a plus Flexible hours - schedule can be tailored as required. Principal Investigator (MD/DO) The Principal Investigator will con...

Sub-Investigator (Nurse Practitioner)    The  Sub-Investigator  is accountable and responsible for ensuring adherence to protocol requirements, protecting the rights and welfare of subjects, assuring the integrity of subject generated data and directing the conduct of research ac...

KNOWLEDGE & EXPERIENCE Education: Bachelor’s degree preferred Advanced degree preferred Experience: At least 4 years of clinical research coordinator experience, including 2 years of management experience at a clinical research organization. Credentials: Certified Clinical Research Coordin...

Identify, establish, and recommend data mapping and design to standardize and harmonize large clinical datasets (including real world data) from multiple American Heart Association clinical trials, research studies and registries as well as other large external datasets. Minimum of two (2) years ...

Occasionally attending out-of-town Investigator Meetings Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent Facilitate...

May act, in concert with senior clinical personnel, as the company spokesperson regarding publication of clinical research findings. Title: Senior Scientist Clinical Research. Senior Scientist Clinical Research. Contributes to the interpretation, reporting and preparation of oral and written resu...

Responsible for providing Clinical Research support for all clinical trials. Responsible for procurement of budgets, contracts, regulatory documents, and other administrative documents as related to clinical research functions. Under the direction of supervisor or designee, this position will ser...

Biotrial is a leading Contract Research Organization (CRO) specializing in Drug Development with a wide range of expertise in preclinical pharmacology, clinical development, bioanalysis, biometrics and ECG, and CNS and Imaging Core Lab. In this position, you will be the main contact for the spons...

We are looking for a per diem Phlebotomist to join our Clinical Research Team. ...

Work Location:   Newark, NJ Responsibilities: Reporting to the Director of Clinical Research Operations, provide support, establish workflows and processes to for high-quality clinical research activities for various Oncology Phase 2 through 4 trials. Association of Clinical Research Profession.....

The Clinical Research Coordinator III will serve as a member of the Clinical Research team. This position is responsible for coordinating and supporting the regulatory affairs activities encountered in clinical research trials conducted by the Clinical Research Center. Rutgers, The State Universi...

As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a m...

Senior Clinical Research Associate. Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

The SCRA collaborates with the Clinical Study Teams (CSTs) by supporting day to day clinical study activities, departmental tasks, and provides mentoring to other CRA team members within established protocols and portfolio under general supervision. Works with Clinical Trial Oversight Managers (C...

The Medical Evidence Generation (MEG) Clinical Research Collaborations team actively bridges Bristol Myers Squibb to the best external science through collaborations with external research entities and networks of practicing clinicians. The Director, Clinical Research Collaborations Lead, will co...

Required Skills: Minimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance and data management. Job Responsibilities: Under the direct supervision of th...