![Pfizer](https://media.trabajo.org/img/noimg.jpg)
Clinical Research Physician
2 months ago
ROLE SUMMARY
The Clinical Research Physician will act as an Investigator and/or Principal Investigator for clinical trials conducted in the PCRU and has responsibilities and accountabilities for trial oversight involving all clinical and medical aspects of study conduct. The Clinical Research Physician is a practicing clinician and member of the PCRU team ensuring 24/7 safety coverage of study participants.
Key accountabilities:
As an Investigator
- Assumes accountability for all medico-legal, scientific integrity, human safety and medical governance aspects of PCRU studies.
- Liaises with other Pfizer sites/line functions regarding the design, conduct and progression of studies in the PCRU.
- Assists with the medical and clinical oversight of all aspects of function and work performed within the PCRU.
- Participates in the planning, execution and data review for allocated studies.
- Works directly with clinical research personnel in reviewing data, performing physical assessments, medical histories, and evaluation of inclusion/exclusion criteria for study participants.
- Participates actively in the review/correction/update and approval of study data, especially the review and coding of adverse events and concomitant medications.
- Supports the implementation and application of electronic health record system (PIMS) in the PCRU.
- Supports the development of Informed Consent Documents for allocated studies and assists in obtaining the consent from study participants.
As a Principal Investigator
- Assumes accountability and responsibility for the execution of the allocated clinical trials.
- Facilitates and coordinates the conduct of Phase I-IIa-IV studies, including Early Development and Full Development Clinical Pharmacology studies (protocol development, review, Regulatory and IEC submissions).
- Provides support for the preparation of clinical protocols, integrated clinical and statistical summary reports, and other documents as requested.
- Participates in the review of source data and/or data listings of safety data, including adverse experiences, laboratory data, and vital signs data, to establish the presence or absence of abnormal trends, and if noted, follow-up as appropriate with the PCRU clinical team, the PCRU project team, the sponsoring Pfizer site, and regulatory agencies.
- Participates in the review of concomitant medication and individual adverse event reports for accuracy and clinical importance, and characterizes their relationship to the study drug, severity and seriousness.
- Ensures that all established timelines relating to areas of responsibility and assigned projects are met.
- Ensures that the quality standard of clinical work product is met.
- Develops a good working knowledge of study management and a full understanding of ICH-Good Clinical Practice and Pfizer SOPs, Work instructions and guidance.
- Develops a good working knowledge of clinical trial activities within the industry and passes this on to less experienced staff.
- Liaises with University Hospitals as necessary in their areas of expertise and joint projects.
- Develops productive working relationships with hospital colleagues and with colleagues at the PCRU and at other Pfizer sites to facilitate the performance of the duties and continued development as a Clinical Research Investigator.
- Develops familiarity with the practice of pharmaceutical medicine through the literature and by attending appropriate trainings, meetings and conferences.
- Liaises effectively with all members of the PCRU and makes a positive contribution towards team spirit in the PCRU.
- Performs regular On-Call/Duty tasks to ensure continuous medical/clinical coverage supporting the conduct of clinical trials in the PCRU.
- Additional responsibilities after acquisition of relevant experience in Phase 1 clinical research activities.
- Represents the PCRU on company-wide initiatives in their area(s) of expertise.
- Represents Pfizer in external environments (e.g., scientific meetings, advisory meetings, etc.) in their area(s) of expertise.
- Develops, maintains and shares subject matter expertise on Clinical Pharmacology and/or Biomarker Methodology topics and studies.
- Act as the expert Physician in Phase 1 clinical research for Worldwide Research and Development, Global Product Development, Clinical Development and Operations, and participates on/contributes to global clinical research committees (e.g. CPSDC).
Training
- Participates in training courses related to clinical research, pharmaceutical medicine, pharmacology as appropriate.
- Assists in the training of PCRU staff and contractors with less experience and expertise.
- Develops knowledge to be responsible for compliance with Pfizer Standards, ethical standards, ICH, regulatory and legal requirements, national and international laws on health and safety at work, fire prevention and other appropriate legislation.
Basic Qualifications
- Medical Degree (MD or DO), with a valid license to practice medicine required. Must have, or clearly be able to obtain, an unrestricted license to practice medicine in the state of Connecticut and be able to successfully complete a standard medical credentialing process as needed.
- Board eligible or board certified preferred; equivalent experience may be considered.
- At least 2 to 3 years of independent (e.g. outside of a formal training program) clinical care experience required, preferably with part of it in clinical trials.
Preferred Qualifications
- Knowledge of local and international drug development regulations (FDA, EMA) and process is an asset.
- Evidence of continuing education/training relative to drug development/study conduct/pharmaceutical medicine is a plus.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
- Serves as a contributor to the on call-schedule to maintain 24/7 unit coverage.
ORGANIZATIONAL RELATIONSHIPS
- Provide the primary groups or key role(s) that this role will interact with as a regular part of the role responsibilities. Include any external interactions as appropriate.
- Reports to Sr. Director Global Head of PCRU Clinical Operations.
- Networks and collaborates with other Pfizer CRUs to ensure organizational consistency of standard operating procedures.
Other Job Details:
- Functional relationship to the Clinical Services Director, Business Operations Director, Pharmacy and Regulatory Directors, Medical and Scientific Advisor, and Safety Laboratory Head in areas of safety, ethical and regulatory oversight for study participants.
- Matrixed relationships to study team and other peers in the PCRU (provides guidance for group study management activities), varied Pfizer scientists and clinicians to design protocol, and multiple other Pfizer colleagues and departments (Dev. Ops., Assay Laboratory, Pharm. Sciences) to implement and report outcomes.
- Operations point of contact for internal departments, external consultants, technical equipment and supply vendors.
- Act as PCRU Representative towards other Pfizer and non-Pfizer departments and customers.
- Collaborates across Pfizer Development and Discovery departments.
Eligible for Employee Referral Bonus: YES
Eligible for Relocation Package: YES
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Work Location Assignment:On Premise
#LI-PFE
The annual base salary for this position ranges from $173,300.00 to $280, In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 22.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits ). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.
Medical
#LI-PFE
View or Apply
To help us track our recruitment effort, please indicate in your email – cover/motivation letter where ) you saw this job posting.
-
Neuroscience Clinical Research Specialist
4 days ago
New Haven, Connecticut, United States Calyx Full timeAbout CalyxOur mission is to redefine the landscape of clinical research. With extensive expertise and a team of exceptional professionals, we assist the global biopharmaceutical sector in expediting the introduction of innovative medical therapies to the market.We aspire to make a significant impact on the world, and with the collaboration of our teams...
-
Clinical Research Lead
4 days ago
New Haven, Connecticut, United States CALYX Full timeExciting Opportunity for a Clinical Research LeadOverviewWe are seeking a dedicated physician to become an integral part of our innovative team at CALYX, a leader in clinical research and medical imaging. In the role of Clinical Research Lead, you will be instrumental in advancing the development of transformative therapies aimed at enhancing patient care....
-
Clinical Research Coordinator
4 days ago
New Haven, Connecticut, United States eTeam Full timePosition: Clinical Trials AssociateCompany: eTeamContract Duration: 18 monthsCompensation: $32/hourAvailability:Weekdays: Flexible shifts including 7:30am-4:00pm, 9:00am-5:30pm, and 10:00am-6:30pmWeekends: As required based on recruitment activity, with prior notice.Qualifications:• At least 3 years of experience in a clinical environment (research or...
-
Clinical Research Coordinator
4 days ago
New Haven, Connecticut, United States eTeam Full timePosition: Clinical Research CoordinatorCompany: eTeamRole Overview:The Clinical Research Coordinator is responsible for facilitating the enrollment of new and existing participants in clinical trials. This role involves executing a variety of pre-screening assessments to establish eligibility for participation in research studies. The Coordinator will...
-
Clinical Research Associate I
5 days ago
New Haven, Connecticut, United States Yale School of Medicine Full timePosition Overview: The Clinical Research Associate I (CRA) will be an integral member of the clinical research team at the PRIME Clinic and Treatment Program. This role encompasses a variety of responsibilities, including assisting in the recruitment of participants for research studies, organizing schedules, preparing necessary materials for study...
-
Clinical Research Coordinator- Epilepsy
1 month ago
New Haven, Connecticut, United States Yale University Full time1. Compares protocols and sponsored projects to confirm consistency between funding proposals/awards and approved protocols. 2. Documents established congruency between funding proposals and approved protocols. 3. Facilitates and/or assists with resolution of any inconsistencies between funding proposals and approved protocols. 4. Serves as a liaison between...
-
Business Analyst for Clinical Research
4 days ago
New Haven, Connecticut, United States Yale University Full timePosition Overview:This role involves the assessment and evaluation of both business and technical specifications to establish the objectives and scope for new or ongoing clinical trials.Key Responsibilities:- Collaborate closely with study teams to collect requirements.- Develop procedures to address intricate challenges in clinical...
-
Clinical Research Participant Coordinator
4 days ago
New Haven, Connecticut, United States Pioneer Data Systems Full timePosition Overview:Our client, a leading Pharmaceutical Company, is seeking a Clinical Trials Patient Recruiter to enhance their growing team.Position Details:Job Title: Clinical Trials Patient RecruiterDuration: 6 months contract, extendable up to 36 monthsWork Schedule:Mon-Thu: 7:30am-4:00pm; 9:00am-5:30pm; 10:00am-6:30pmFri: 7:30am-4:00pm; 8:00am-4:30pm;...
-
Clinical Research Analyst II
4 days ago
New Haven, Connecticut, United States Yale University Full timePosition Overview:This role involves the thorough examination and evaluation of both business and technical specifications to establish the scope and objectives for ongoing or upcoming clinical trials.Key Responsibilities:1. Collaborate closely with study teams to collect and articulate requirements.2. Develop procedures to address intricate challenges...
-
Clinical Research Participant Coordinator
4 days ago
New Haven, Connecticut, United States Pioneer Data Systems Inc Full timePosition Overview:Pioneer Data Systems Inc is seeking a dedicated Clinical Trials Patient Recruiter to support our clinical research initiatives.Role Details:Job Title: Clinical Trials Patient RecruiterContract Duration: 6 months, with potential for extensionWork Schedule: Monday to Thursday, with flexible hours; Saturday work as requiredKey...
-
Clinical Research Participant Coordinator
4 days ago
New Haven, Connecticut, United States Pioneer Data Systems Inc Full timePosition Overview:Pioneer Data Systems Inc is seeking a dedicated Clinical Trials Patient Recruiter to enhance our clinical research initiatives.Position Details:Job Title: Clinical Trials Patient RecruiterContract Duration: 6 months, with potential for extension up to 36 monthsWork Schedule: Monday to Thursday: 7:30 AM - 4:00 PM; 9:00 AM - 5:30 PM; 10:00 AM...
-
Clinical Research Participant Coordinator
4 days ago
New Haven, Connecticut, United States Pioneer Data Systems Full timeOur client, a prominent Pharmaceutical Company, is seeking a Clinical Trials Patient Recruiter to enhance their growing team.Position Overview:Job Title: Clinical Trials Patient RecruiterDuration: 6 months contract, extendable up to 36 monthsLocation: New Haven, CTWork Schedule:Mon-Thu: 7:30am-4:00pm; 9:00am-5:30pm; 10:00am-6:30pmFri: 7:30am-4:00pm;...
-
New Haven, Connecticut, United States Synectics Inc Full timeJob OverviewPosition Summary:The Clinical Research Participant Engagement Specialist is tasked with onboarding both new and existing clinical trial participants, executing a range of preliminary screening processes to assess eligibility for various clinical studies.This role involves implementing recruitment strategies while adhering to regulatory standards...
-
Full Time Physician Assistant
3 months ago
New Haven, Connecticut, United States Enterprise Medical Recruiting Full timeExcellent opportunity exists for an experienced Hematology/Oncology Nurse Practitioner or Physician Assistant to see a broad spectrum of Hematology/Oncology patients in the office and hospital. Will consider APRN's with previous nursing experience in Hematology and Oncology. The Job:Monday through Friday, 40 hour scheduleMostly outpatient coverageNo...
-
Full Time Hematology and Oncology Physician
1 month ago
New Haven, Connecticut, United States Enterprise Medical Recruiting Full timeWe are hiring a Hematology/Oncology PhysicianOne of the major healthcare institutions in Connecticut is looking to add a Hematology/Oncology Physician to their team.Practice DetailsJoin a healthcare network of over 4000 Providers and 7 hospitalsWork at an 867-bed teaching hospital with a level 1 trauma centerLooking for a candidate interested in contributing...
-
Full Time Anesthesiology Physician
3 months ago
New Haven, Connecticut, United States Merritt, Hawkins & Associates Full timeJob Description & RequirementsCT - ICU Anesthesiologist in ConnecticutStartDate: ASAP Pay Rate: $ Merritt Hawkins Department of Academic Recruiting has partnered with YaleSchool of Medicine Department of Anesthesiology to find board-certified,fellowship-trained critical care anesthesiologists with experience in critical caremanagement of cardiothoracic...
-
Full Time Neurology Physician
3 months ago
New Haven, Connecticut, United States Enterprise Medical Recruiting Full timeExciting Opportunity - Neurohospitalist Position in Large and Innovative Connecticut Neurology GroupJoin an inpatient team with a 7 on/7 off scheduleWork 12-hour shifts alongside a team of top healthcare professionals, including Neurologists, Neurosurgeons, Specialists, and Physician AssistantsContribute to cutting-edge research and provide comprehensive...
-
Research Associate 2
1 month ago
New Haven, Connecticut, United States tapwage Full timeSTARS Requisition number89060BRPosting Position TitleResearch Associate 2Essential DutiesDesigns, plans, implements and evaluates complex multifaceted research projects/systems, including method development, adaptation and validation. 2. Collaborates with PI to define research endeavors and the development of research hypothesis and approach. 3. Solves...
-
Clinical Trials Participant Recruiter
4 days ago
New Haven, Connecticut, United States Pioneer Data Systems Full timePosition Overview:Our client, a prominent Pharmaceutical Company, is seeking a dedicated Clinical Trials Patient Recruiter to enhance their expanding workforce.Key Responsibilities:Job Title: Clinical Trials Patient RecruiterContract Duration: 18 monthsRole Focus: Engage with potential participants for clinical studies, ensuring a thorough understanding of...
-
Clinical Trials Recruitment Specialist
4 days ago
New Haven, Connecticut, United States Pioneer Data Systems Full timePosition Overview:Our client, a prominent player in the pharmaceutical sector, is seeking a dedicated Clinical Trials Patient Recruiter to enhance their team.Key Responsibilities:Identify and engage potential participants for clinical trials.Utilize various recruitment strategies to attract suitable candidates.Maintain accurate records of participant...