What are the responsibilities and job description for the Clinical Research Physician ONSITE in Dallas Texas position at Fortrea?
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.Come expand and grow your potential leadership and skills at Fortrea as an (onsite) Clinical Research Physician at our Dallas, Texas location supporting clinical trials. The Clinical Research Physician (CRP) reports to onsite Medical Director and one of the major functions of the role is communication and interaction with participants, regulatory bodies, and clinical teams along with other departments within Clinical Pharmacology.Job Summary : This role will provide an information service and knowledge base on the clinical aspects of clinical trials in Clinical Pharmacology. In addition, incumbent may act as a sub-investigator.Key Responsibilities : Provides onsite medical coverage for Clinical Research Unit for our Dallas, Texas site Protect the rights, safety and welfare of participants under their careEnsure that the clinical trial is conducted according to the investigational plan and all applicable regulationsAdministers test article to the subjects, or delegates this to nursing staff where appropriateReview and evaluate protocols and provide clinical and scientific supportInteract with regulatory bodies as is relevant to clinical operationsAttend study initiation meetings.Present protocols at IRB / IEC meetings, as requiredAssist Operations and Client Managers with sponsor visitsPerform pre-study physical examinations and review lab data and all inclusion / exclusion criteria to ensure volunteers are medically and mentally fit upon entering the studyPerform on-study and post-study physical examinations to ensure that the physical and mental well-being of volunteers is undiminished at the end of the studyInform Principal Investigator, IRB / IEC and Sponsor as appropriate of relevant eventsReview and sign CRFs at the conclusion of the studyDelegate the above as appropriateAct as Principal Investigator / Co-Investigator as assigned by the Medical DirectorEducationMD or DO degreeActive and unrestricted Texas Medical License and DEAACLS / CPR / AED CertifiedExperienceMinimum of 2 years of clinic / patient care experienceSpecialization in Family Medicine and or Primary Care preferred. Previous Clinical Trials experience is preferredAbility to work in a fast-paced environmentStrong interpersonal and communication skillsMust have current active TX license#LI-SE1Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.Fortrea is proud to be an Equal Opportunity Employer : As an EOE / AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions / needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.For more information about how we collect and store your personal data, please see our Privacy Statement. If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact : taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
