502 matching jobs for “Business Development Representative – Data Foundation”How results work Exact titles rank first, then title variations and keywords in descriptions. These labels aren't qualification scores. Without keywords, recently added jobs appear first.
… obtain INTERIM U.S. government issued security clearance is required prior to start date At Raytheon, the foundation of everything we do is rooted in our values and a higher calling – to help our nation and allies defend …
Added Oct 27, 2026
+5 locations
Pay posted by employer $239,900–$399,800 per year
The medical director provides Clinical Development leadership and expertise on Late phase clinical trials, including overseeing the design, conduct, and …
Added Oct 16, 2026
… obtain INTERIM U.S. government issued security clearance is required prior to start date At Raytheon, the foundation of everything we do is rooted in our values and a higher calling – to help our nation and allies defend …
Added Oct 27, 2026
+6 locations
The Clinical Development Medical Director will provide medical and scientific leadership for a Phase 3 oncology clinical trial …
Added Oct 16, 2026
… obtain INTERIM U.S. government issued security clearance is required prior to start date At Raytheon, the foundation of everything we do is rooted in our values and a higher calling – to help our nation and allies defend …
Added Oct 27, 2026
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
+1 location
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
+2 locations
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
+1 location
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
Analyze manufacturing business processes and convert operational requirements into scalable Eyelit MES models and workflows. Translate …
Added Oct 27, 2026
… minds in the industry? At RTX , our internships, co-ops and full-time careers provide an exceptional foundation to work on complex problems, advance your skills and create a safer, more connected world. Discover …
Added Oct 27, 2026
… and inclusion are at the core of Disney, defining the experience that we deliver as well as providing the foundation of our success. The scope of our business, combined with global growth and collaboration result in an …
Added Oct 27, 2026
+2 locations
… Senior Platform Engineer will lead the design, operation, and continuous improvement of the organization’s data and platform services across a complex portfolio of cloud, analytics, and AI-enabled workloads. This role …
Added Oct 27, 2026
+2 locations
Pay posted by employer $44,000–$185,000
… This exact role may not be open today but could open in the near future. When you apply, a Cisco representative may contact you directly if a relevant position opens. Applications are accepted until further notice. This …
Added Oct 27, 2026
+4 locations
… problems. With our three market leading businesses, world-class operations and investments in research and development , we offer capabilities and opportunity no one else can. Together, we push the boundaries of known science …
Added Oct 27, 2026
+1 location
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
+1 location
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
+1 location
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
+1 location
Pay posted by employer $55,000–$60,000 per year
… existing accounts Build and manage a territory pipeline, maintaining accurate activity and opportunity data in the CRM Execute in-clinic education, product demonstrations, and follow-up with clinical staff Meet or …
Added Oct 15, 2026
+6 more
Basic Qualifications · employer excerpt As medically qualified individual, the successful candidate must have the following qualifications: Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university and has 4+ years of experience. Been licensed by a licensing body/health authority to prescribe medicines independent of Supervision… Clinical training and meaningful patient-care experience in oncology. Clinical research or drug-development experience in the pharmaceutical industry, biotechnology industry, academia, or a comparable environment. Working knowledge of clinical trial design, conduct, analysis, and interpretation. 4 more in the full description below.
About this opportunity Original employer description Job Summary The Clinical Development Medical Director will provide medical and scientific leadership for a Phase 3 oncology clinical trial within prostate cancer.
The Clinical Development Medical Director will work in close partnership with the Clinical Scientist and cross-functional study team to oversee study conduct, medical monitoring, safety evaluation, data interpretation, and delivery of high-quality clinical and regulatory documents. The individual will also contribute to broader clinical development planning and ensure that study-level decisions remain aligned with the overall program strategy.
The role requires strong clinical judgment, scientific rigor, and the ability to lead through influence across a global matrix organization. The Medical Director will engage with investigators, external experts, health authorities, internal governance bodies, and colleagues across Clinical Operations, Safety, Regulatory Affairs, Biostatistics, Clinical Pharmacology, Medical Writing, and other partner functions.
Key Responsibilities Study-Level Clinical Development Leadership Provide medical and scientific leadership for a Phase 3 oncology clinical trial within prostate cancer Partner with the Clinical Scientist and Clinical Study Team Lead to support effective study execution and delivery. Ensure that study conduct and clinical decisions are scientifically rigorous, clinically appropriate, and aligned with the clinical development plan. Provide medical input into study strategy, protocol implementation, operational decisions, and risk-mitigation plans. Identify emerging clinical or scientific issues and bring forward clear, evidence-based recommendations. Represent Clinical Development in study-team and cross-functional discussions. Escalate material clinical, safety, quality, or operational risks to program leadership and appropriate governance bodies Medical Monitoring and Patient Safety Serve as the Medical Monitor for the assigned clinical trial. Conduct medical monitoring activities, including eligibility consultation, medical review of participant data, protocol deviation assessment, and ongoing safety surveillance. Provide timely medical guidance to investigators, study teams, and clinical operations colleagues. Review and interpret adverse events, laboratory abnormalities, dose modifications, treatment interruptions, and other clinically significant findings. Partner with Safety to evaluate emerging safety signals and support benefit-risk assessments. Contribute to the development and implementation of appropriate safety-monitoring and risk-mitigation measures. Support aggregate safety reviews, safety governance discussions, and interactions with independent data-monitoring committees, as applicable. Clinical Data Review and Interpretation Collaborate with the Clinical Scientist, Biostatistics, Programming, Safety, and other team members to establish and execute clinical data-review plans. Review and interpret efficacy, safety, patient-reported outcome, imaging, and other relevant clinical data. Identify clinically meaningful trends, data-quality issues, inconsistencies, and areas requiring further analysis. Provide medical interpretation of study results and communicate their implications to cross-functional stakeholders. Contribute to data-cut planning, interim analyses, database-lock readiness, and final study analyses. Support scientifically and regulatorily defensible interpretation of primary, secondary, and exploratory endpoints. Clinical and Regulatory Documents Lead or contribute to the development, review, and maintenance of:Clinical study protocols and amendments Investigator’s Brochures Informed-consent documents Medical-monitoring plans Clinical Study Reports Integrated clinical and safety summaries Regulatory briefing documents Health-authority questions and responses Risk-management and safety-communication materials Publications and scientific presentations Ensure that clinical interpretations and conclusions are accurate, balanced, internally consistent, and supported by available evidence. Collaborate closely with Medical Writing, Regulatory Affairs, Safety, Biostatistics, and other functions to deliver high-quality documents according to program timelines. Regulatory and Governance Support Provide clinical and medical input into global regulatory strategy for the assigned study. Support preparation for and participation in health-authority interactions. Present study status, emerging data, clinical risks, and recommendations to internal governance bodies, as appropriate. Clearly communicate areas of uncertainty and provide balanced recommendations for decision-making. Support inspection readiness and provide clinical rationale and documentation for key study decisions. Ensure that important decisions and deviations from planned approaches are appropriately documented. Investigator and External Engagement Lead peer-to-peer medical interactions with investigators. Serve as a point of contact for clinical questions involving the study team, investigators, steering committees, ethics committees, and regulatory authorities. Participate in investigator meetings, advisory boards, scientific congresses, and other external engagements. Develop trusted relationships with investigators and external experts while maintaining appropriate scientific and compliance standards. Maintain current knowledge of prostate cancer treatment, clinical practice, relevant literature, evolving standards of care, and the competitive development landscape. Cross-Functional Collaboration Work closely with:Clinical Scientists Clinical Operations Biostatistics and Programming Pharmacovigilance and Safety Regulatory Affairs Clinical Pharmacology Translational Oncology Medical Writing Data Management Health Technology Assessment and Evidence colleagues Medical Affairs Build alignment across functions while maintaining an independent medical and scientific perspective. Contribute constructively to program-level discussions, planning activities, and risk assessments. Promote consistent clinical approaches across studies when scientifically and operationally appropriate. Support and mentor Clinical Scientists and other study-team colleagues. Basic Qualifications As medically qualified individual, the successful candidate must have the following qualifications:
Obtained a primary medical degree (e.g., MD, DO, MBBS, MBChB) from a recognized medical school/university and has 4+ years of experience. Been licensed by a licensing body/health authority to prescribe medicines independent of Supervision for at least 2 years post their intern/house officer/foundation period. Clinical training and meaningful patient-care experience in oncology. Clinical research or drug-development experience in the pharmaceutical industry, biotechnology industry, academia, or a comparable environment. Working knowledge of clinical trial design, conduct, analysis, and interpretation. Understanding of Good Clinical Practice and applicable ethical and regulatory requirements. Ability to interpret complex clinical and safety data and translate findings into clear medical recommendations. Strong written and verbal communication skills. Demonstrated ability to collaborate and influence in a cross-functional matrix environment. Preferred Qualifications 2+ years experience in industry. Board eligibility or board certification in Medical Oncology, Hematology/Oncology, Urology, or another relevant specialty preferred Prostate cancer clinical or drug-development experience. Experience supporting Phase 3 or registration-enabling oncology trials. Prior experience serving as a study Medical Monitor. Experience evaluating oncology efficacy endpoints and imaging-based assessments. Experience working with blinded independent central review and radiographic progression-free survival endpoints. Experience supporting regulatory submissions or health-authority interactions. Experience contributing to Clinical Study Reports, integrated summaries, Investigator’s Brochures, protocols, and regulatory responses. Experience with independent data-monitoring committees or other safety-governance bodies. Familiarity with global oncology trial execution and interactions with investigators across multiple regions. Ability to present complex clinical issues and recommendations to senior governance audiences.
Work Location Assignment: This is a hybrid role requiring you to live within commuting distance and work on-site an average of 2.5 days per week.
Relocation assistance may be available
The annual base salary for this position ranges from $239,900.00 to $399,800.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% 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 | (uscandidates.mypfizerbenefits.com). 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.

This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview.


Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
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. This position requires permanent work authorization in the United States.
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected] . This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
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