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| | | We currently do not have any open positions that match your criteria, but new positions could become available at any time. Below is a sampling of the type of positions that we have had available in the past that match your search criteria. | | |
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 | Location  | City | Job Type | Job Title | Category | Status |  |
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| DE | Wilmington | Temporary | Director / Executive | Clinical | Filled | | | Delta Pharma is a national leader in the staffing of professionals in the Pharmaceutical, Biotech, and Medical Device industries. Managing the professional staffing needs of leading Pharma companies nationwide, we take pride in bringing Great People and Great Opportunities together.
Come be a part of our success story!
Job Title
Position Description
- Will be working with internal and external customers, including Clinical Project Teams, Global Product Teams, Therapy Areas, Global Marketing and Business Development, Regulatory, and FDA to accomplish tasks related to the product development, to improve clinical development processes, and to ensure satisfaction of these customers.
- Brand Physician: Serves as a source of medical expertise for the assigned Brand Team;
- Provide medical expertise for Life Cycle Development and claims development. Provide medical guidance to Brand Teams for creation of promotional and promotion-related training materials.
Position Responsibilities
- Serves as a source of medical expertise for the assigned Brand Team.
- Provide medical expertise for Life Cycle Development and claims development.
- Provides medical guidance to Brand Teams for creation of promotional and promotion-related training materials.
- Give guidance for Phase IV and investigator initiated trials in cooperation with regional marketing companies.
- Responsible (in collaboration with other Team members) for medical components of study protocols, labeling and regulatory communications under the direction of the Medical Science Director.
- Responsible to establish communications with prominent clinical investigators in his/her particular field of expertise, particularly those who will be willing and able to assist in the evaluation of the company's products in accordance with Brand Team objectives.
- Work with international colleagues on research initiatives and regulatory issues.
- Applies strategic intent of the company when working with FDA, opinion leaders, prescribers and consumers of company products.
- Assumes other duties as assigned by the Group Director.
Position Requirements - Graduate of a recognized school of medicine with an M.D. degree or equivalent.
- Specialty training and board certification in Internal Medicine; Endocrinology; Diabetes and Metabolism; or Cardiovascular Medicine
- Prior clinical experience and strong academic track record in cardiovascular disease and metabolic disorders required
- Three or more years of Drug Development experience obtained while working in the pharmaceutical industry with focus and expertise in cardiovascular and metabolic disorders required for Director level position.
- Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including understanding of biostatistics and safety reporting.
- An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence those decision points.
- An understanding of the interplay between clinical development and commercial objectives.
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | IL | Deerfield | Permanent | Director / Executive | Clinical | Filled | | | Delta Pharma is a national leader in the staffing of professionals in the Pharmaceutical, Biotech, and Medical Device industries. Managing the professional staffing needs of leading Pharma companies nationwide, we take pride in bringing Great People and Great Opportunities together.
Come be a part of our success story!
Job Title
- Medical Director, Pharmacovigilance Physician
Position Description
- This position is responsible for strategies in pre and post marketing risk management, as well as keeping abreast of pharmacovigilance methods and trends in published literature and global regulations. Additionally responsible for strategies in monitoring and analysis of cumulative safety information on company products. Responsible for drug safety crisis management.
Position Responsibilities
- Guides regulatory reporting including individual case safety reports (ICSRs), NDA annual report summary statements, and Periodic Safety Update Reports (PSURs)
- Guides adverse event coding, retrieval and analysis activities in drug safety and clinical trials
- Guides reviews of safety sections of NDA submissions
- Plans cumulative safety information analysis such as signal detection from company or public databases with data mining
- Guides safety updates of company core data sheet and local product labels
- Guides pharmacoepidemiology projects
- Guides crisis management on drug safety
- Guides Risk Management Plans for specific products
- Guides and coordinates preparation of ad-hoc benefit-risk assessment documents
- Guides regulatory strategy and preparation of data related safety to regulatory authorities and advisory committees.
- Interfaces with Medical Sciences, Clinical Studies, Product Safety Management, Drug Development and Project Management, Pharmacoepidemiology, Global Pharmacovigilance departments, Toxicologist, Biopharmaceutical sciences, Research Data Sciences, Legal
Position Requirements - MD degree, Pharmaceutical Industry experience in Pharmacovigilance and drug safety for at least five years, Team working, analytical skills, and flexibility are essential for this position.
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | IL | Westmont | Permanent | Director / Executive | Clinical | Filled | | | Delta Pharma is a national leader in the staffing of professionals in the Pharmaceutical, Biotech, and Medical Device industries. Managing the professional staffing needs of leading Pharma companies nationwide, we take pride in bringing Great People and Great Opportunities together.
Come be a part of our success story!
Job Title
- Director Business Development (Clinical Software)
Position Description - Delta-Pharma is seeking a Software Business Development expert to support the development west coast pharmaceutical and biotech client base for a well known client.
- Supported by a team of Clinical Operations experts, this position will be responsible to further expand the west coast region, selling CTMS software.
- This position is a homebased sales opportunity that does not have to be based out of the west coast.
Position Responsibilities - Develop and execute on account strategies
- Prospecting, lead gen/qualification, customer presentations driving/managing the sales cycle
- Forecasting based on opportunity assessment
- Maintain strong relationships and satisfaction among existing customers
- Providing feedback from customers and prospects to the product management group
- Drive sales – through existing industry relationships and networking
Position Requirements - 10+ years as a sales/business development professional selling into clinical operations departments of pharmaceutical/biotech companies
- Business development with a major CRO a plus
- 7+ years software sales experience in an enterprise software sales environment
- Experience in clinical operations, costing, and clinical trial project management
- Strong technical, software acumen and abilities
- Entrepreneurial, high energy, self-motivated, assertive; consummate professional
- Bachelors Degree
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | IL | Libertyville | Permanent | Director / Executive | Clinical | Filled | | | Delta Pharma is a national leader in the staffing of professionals in the Pharmaceutical, Biotech, and Medical Device industries. Managing the professional staffing needs of leading Pharma companies nationwide, we take pride in bringing Great People and Great Opportunities together.
Come be a part of our success story!
Job Title
- Medical Director, Post-Marketing Safety
Position Description
- The candidate will monitor and summarize post-marketing adverse events; maintain all aspects of medical safety for selected product lines.
Position Responsibilities
- Provide medical review of labeling and brochures,
- Author reports for regulatory submissions based upon case review, data mining, case series analysis, etc.
- Develop, mentor and lead a group of physicians within Post-marketing Safety Evaulation.
Position Requirements - MD, board certification is highly preferred, but board eligibility will be considered.
- 5 years of pharmaceutical industry experience and experience managing MD's.
- Residency with direct patient management.
- Licensure in the US is preferred.
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | IL | Abbott Park | Permanent | Director / Executive | Clinical | Filled | | | Delta Pharma is a national leader in the staffing of professionals in the Pharmaceutical, Biotech, and Medical Device industries. Managing the professional staffing needs of leading Pharma companies nationwide, we take pride in bringing Great People and Great Opportunities together. Come be a part of our success story! Job Title - Medical Director, Clinical
Position Description
- Identify, assess and appropriately manage safety signals Phase 1- Phase 4.
Position Responsibilities
- Review safety reports and safety sections for labels. Possess familiarity with biostatistics and computer data processing techniques. Must have strong interpersonal and leadership skills, self motivation, integrity, ethics and a solid commitment to drug safety.
- Review and evaluate serious event reports
- Communicate safety assessments
- Medical review for safety sections of protocols, study reports, labels and investigator brochures.
- Work with Quality Assurance, Document Management, Clinical teams, Legal,and Regulatory Affairs
Position Requirements - Associate Director- 1 to 3 years of clinical experience within a private practice or academic medical setting.
- Medical Director- 2 years of drug safety experience:
- Senior Medical Director requires 5 years.
- MD/DO board certified in internal medicine or family medicine is preferred.
- Clinical pharmacology or clinical trial experience is also preferred.
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | Ma | Cambridge | Temporary | Director / Executive | Clinical | Filled | | | Delta Pharma is a national leader in the staffing of professionals in the Pharmaceutical, Biotech, and Medical Device industries. Managing the professional staffing needs of leading Pharma companies nationwide, we take pride in bringing Great People and Great Opportunities together.
Come be a part of our success story!
Job Title
- Associate Medical Director, Pharmacovigilance
Position Description - Supports Global Pharmacovigilance with an emphasis on medical review of adverse events.
Position Responsibilities - Handle adverse events according to national and international regulatory requirements and as per the departmental and corporate SOPs
- Ensure adequacy of recording, summarizing, and handling of adverse events for both investigational and marketed products including decisions on seriousness and expectedness and causality
- Ensure accuracy and timeliness of expedited reports from postmarketing safety surveillance and from clinical trials
- Review literature articles (both published and yet to be published) following established procedures
- Ensure accurate MedDRA coding of adverse events from all sources
- Author Similar Even Analysts reports following established procedures
- Review safety sections of clinical trial protocols, investigator brochures, and informed consents for selected drug development programs
- Responsible for Pharmacovigilance signaling activities
- Participation in Pharmacovigilance group meetings
- Attend the clinical team meetings as a Pharmacovigilance representative for responsible products
- Serve as a resource for the Medical Information and Quality Assurance Teams
- Assist and support the activities of the teams, Pharmacovigilance and of Global Pharacovigilance
- Provide expert advice on medical matters in general, and specifically on pre and post-marketing safety-related issues
- Participate and collaborate in the creation and review of Pharmacovigilance Standard Operating Procedures and other documents that support regulatory compliance
- Communicate and collaborate effectively in safety matters with Regulatory Affairs, Clinical Teams, Biostatistics, Data Management, Marketing, and the Legal Department
- Keep management informed of special concerns and developing safety problems with investigational or marketed products
- Collaborate with consultants concerning drug safety issues and pharmacoepidemiology studies
- Provide strategic input to and in certain instances lead safety analyses including, but investigator brochures, and Integrated Summaries of Safety
- Work with Clinical Teams and Project Management and interface with CRO Safety
- Perform such other duties as requested by management
Position Requirements - M.D. degree or equivalent
- MedDRA training (may be provided after starting)
- GCP training (may be provided after starting)
- Graduate training/experiences resulting in board eligibility/certification
- Prior experience in pharmaceutical medical research with specific experience in product safety/pharmacovigilance/benefit-risk optimization
- Postgraduate training in clinical epidemiology and biostatistics
- Specialization and experience in oncology
- Practical clinical experience/expertise
- Individual Case Safety Report handling, as well as periodic report, PSUR and variation preparation
- Expertise in clinical research and safety activities in a pharmaceutical/biotech company
- Practical experience working with MedDRA
- Experience/expertise in pharmacoepidemiology research
- Management experience
- Ability to interact effectively with staff of multiple disciplines both within and outside the company both nationally and internationally
- Ability to manage/supervise activities in a fast paced and changing environment to ensure objectives are met in a timely manner and achieved within budge allocations
- Ability to understand the safety database
- Nature of the department and the information that flows through the group requires that the individual be able to work well and communicate effectively with people both inside and outside of the department in order to meet deadlines.
- Person needs to be able to adapt to the changing dynamics on workflow and react accordingly.
- Due to the sensitive nature of the data received, person must have integrity when handling the confidential data.
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | Ma | Cambridge | Temporary | Director / Executive | Clinical | Filled | | | Delta Pharma is a national leader in the staffing of professionals in the Pharmaceutical, Biotech, and Medical Device industries. Managing the professional staffing needs of leading Pharma companies nationwide, we take pride in bringing Great People and Great Opportunities together.
Come be a part of our success story!
Job Title
- Medical Director - Oncology
Position Description
- The Sr. Director of Oncology Clinical Research provides medical guidance and leadership in the design, implementation, monitoring and interpretation of clinical trials conducted in patients with malignancies. These clinical trials will most often involve the development of new chemical entities (small molecules and biologics) with therapeutic potential, both as single agents, and in combination with existing approved agents. However, some clinical trials may involve the assessment of diseases, with the aim of better understanding disease pathophysiology, potential therapeutic targets, and markers of drug action and disease modification.
Position Requirements
- Practicing Oncologist with at least 2 years experience in Clinical Research
- Board Certified Physician
- Currently Practicing
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | Ma | Cambridge | Permanent | Director / Executive | Clinical | Filled | | | Delta Pharma is a national leader in the staffing of professionals in the Pharmaceutical, Biotech, and Medical Device industries. Managing the professional staffing needs of leading Pharma companies nationwide, we take pride in bringing Great People and Great Opportunities together. Come be a part of our success story! Job Title- Associate Director of Molecular Medicine- Oncology
Position Description- We are seeking a research scientist with experience in oncology drug development to join the Molecular Medicine Department. This person will be responsible for identifying and implementing clinical biomarker opportunities for one or more of our investigational anticancer drug programs
Position Responsibilities/Experience- a)The successful applicant’s responsibilities will include: a) oversee the development and monitor the quality assurance of pharmacodynamic, pharmacogenomic and disease biomarker assays for use in company-sponsored clinical trials,
- b) oversee the design and implementation of biomarker research in clinical trials,
- c) work with medical directors, clinical pharmacologists and nonclinical and discovery research scientists to ensure early definition of, and agreement on biomarker needs for clinical development strategy and
- d) maintain extensive knowledge of the research and development efforts from academic institutions, competitor pharmaceutical companies, and fee-for-service bioanalytical companies for relevant oncology biomarkers.
- Doctoral degree (PhD.) or equivalent, postdoctoral experience and 10+ years of relevant industry experience.
Benefits- Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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