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 | Location  | City | Job Type | Job Title | Category | Status |  |
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| IL | Westmont | Permanent | Clinical Management | Clinical | Open | | | Provide Post Sales Account Management to CTMS customers. Strong understanding of CTMS systems is critical, with a background in clinical research. 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
- Clinical Services Manager
Position Description
- Provide Post Sales Account Management to CTMS customers. Strong understanding of CTMS systems is critical, with a background in clinical research.
Position Responsibilities
- Support the development and implementation of key projects.
Manage, maintain and serve as primary contact for existing customer relationships; - Develop and execute on account strategies
- Identify/confirm the customer’s business needs/drivers
- Identify other potential users (ex. expansion opportunities)
- Identify potential inside competition (ex. systems, initiatives, dissenters, re-organizations)
- Identify consult needs and lead the delivery of Study Consult Services (SCS) to customer
- Expand understanding and use of company’s software within existing customers, including customer’s Executive team
- Identify new opportunities within existing customers (i.e. new products) and secure referrals to other opportunities
Position Requirements - BS/BA degree plus 5 years direct pharmaceutical clinical research experience (primarily as a CRA/Clinical Trials Manager and/or Clinical Operations Manager)
- 5+ years experience in clinical operations, clinical trial project management, clinical trial costing, and/or clinical outsourcing/contract negotiation
- Strong entrepreneurial drive and ability to deliver results with limited supervision
- High energy, self-motivated, assertive; consummate professional
- Good customer presence and presentation skills
- Able to understand/analyze customers [unstated] needs.
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | NJ | Lawrenceville | Temporary | Clinical Management | Clinical | Open | | | 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
· Clinical Scientist
Position Description
· Project Management of Phase I Clinical Trials
Position Responsibilities
- Writing and conducting Ph I clinical trials and/or equivalent experience.
- Delivering on timelines, with exemplary accuracy and attention detail. Demonstrated ability to work independently and with self-motivation.
- Effective scientific presentation skills.
- Negotiation skills.
- Managing budgets.
- Ph I-IV processes, procedures and timelines
- Understanding of data management and statistical analysis process.
- Understanding of project planning and management. Understanding of the pharmaceutical industry
Position Requirements - Candidate with a BA/BS is Preferred
- Must Have 1-3 Years of Pharmaceutical Industry Experience
- Protocol and Project Management in Pharma Industry/Clinical Development
- Protocol Documents and Plan Coordination
- Protocol Documents and Plan Development
- Protocol Management
- Strong Computer
- Strong Interpersonal Skills
- Experience in clinical research in the pharmaceutical or medical industry
- Experience in writing and conducting Ph I clinical trials and/or equivalent experience
- Experience in working in teams
- Experience with delivering on timelines, with exemplary accuracy and attention detail
- Demonstrated ability to work independently and with self-motivation
- Experience with managing budgets
Benefits · Blue Cross/Blue Shield Medical and Vision · Delta Dental · 401K with Company Match · Holidayand Vacation Pay · Relocation Assistance
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| | | PA | Bala Cynwyd | Temporary | Clinical Management | Clinical | Open | | | Leads clinical research trials in accordance with FDA regulations and ICH guidelines, good clinical practices and standard operating procedures and ensures drug development project objectives are met. 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
- Primary purpose and function of this position, under the guidance of the Clinical Trials Manager or Clinical Trials Lead III, leads clinical research trials in accordance with FDA regulations and ICH guidelines, good clinical practices and standard operating procedures, and ensures drug development project objectives are met.
Position Responsibilities - Manages single project; assures that project objectives are met: 50%
- Does project assessment and initiation, resource planning and project implementation
- Assists in the writing and development of protocols and amendments
- Plans and tracks projects and produces key progress reports
- Reviews and tracks regulatory documents at study start-up and during trial
- Develops monitoring tools for CRAs
- Reviews and designs case report forms
- Assures that projects adhere to GCP, CFR, ICH guidelines and SOPs
- Tracks progress of clinical study
- Delegates tasks to clinical project team members
- Authorizes drug shipments and tracks study supplies
- Assists in the development, tracking, and negotiation of contracts for sites
- Serves as back-up and/or primary contact and resource expert for vendors, 35%
- CRAs, investigative sites, local and global team members
- Oversees CRA activity relevant to the project requirements
- Provides project related training
- Provides input regarding team members'performance
- Assists CRA Managers with interviewing candidates
- Oversees communication among CROs, contract CRAs and global team members 10%
- Partners cross-functionally with departments such as Pharmacovigilance 5%
- Pharmacovigilance, QA, Regulatory and CRRC
- Other duties and responsibilities as assigned
- Travel: Approximately 10 - 30%, primarily domestic
Core Competencies - Demonstrates a basic understanding of Clinical Trials conduct
- Demonstrates a basic understanding of ICH and GcP regulations and guidelines
- Demonstrates a basic understanding of assigned protocols and CRF requirements
- Demonstrates solid computer skills including MS Word and MS Excel
- Pro-actively and promptly updates/informs others of relevant concerns verbally and in concise written form
- Responds promptly and follows up to ensure action is taken on recommendations and opportunities
- Produces clear, concise reports with minimum guidance
- Delegates effectively
- Leads, mentors, and assists
- Recognizes contribution of associates and peers
- Leads projects and other work
- Explores and pursues opportunities to improve projects
- Identifies and resolves issues
- Understands goals and initiatives of upper management and integrates into work efforts
- Sets appropriate priorities
- Plans, organizes, manages and monitors activities according to priorities
- Identifies and solves problems proactively, not reactively
- Skillful in negotiation to resolve issues and in gaining cooperation
- Teamwork
Position Requirements - RN or BS degree in allied health or life science or equivalent combination of education and related work
- Education preferred: Bachelor of Science
- Years of experience required: 2 years in-house or external clinical monitoring experience
- Years of experience preferred: 3-4 years applicable experience including some clinical trial management experience, as well as experience with electronic data capture, remote data entry and clinical trial management systems
- Specific experienced preferred: CRA certification
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | We currently do not have any other 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. | | |
| | | CA | Thousand Oaks | Temporary | Clinical Management | 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
- Senior Manager, Medical Communications
Position Description
- The Senior Manager will assist the Medical Communications team to meet critical team deliverables on a part-time basis.
Position Responsibilities - Reviewing weekly assignment Sensipar Mac reviews
- Assisting in RML,POA tools
- Providing scientific content for Brand promotional tools as well as other activities such as comparative intelligence for Congress.
Position Requirements - Extensive scientific knowledge
- PharmD, OD or MD
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holidayand Vacation Pay
- Relocation Assistance
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| | | CA | Thousand Oaks | Temporary | Clinical Management | 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
- Research Operations Project Manager II
Position Description
- Provides support to product teams in the Small Molecule Process and Product Development (SMP&PD) department.
Position Responsibilities - Initiates, plans, executes, monitors and controls, and closes out product project team activities. Informs team lead, functional area lead scientists, project team, and senior management on project status, developments, and issues.
- Acts as a liaison between various departments and outside contract resource organizations (CRO) and consultants, manages and executes contracts by coordinating support from Legal, department management, and scientists.
- Facilitates project communications (e.g. agendas, minutes, action items, documents).
- Applies knowledge and understanding of project needs, recognizing and escalating problems as needed
Position Requirements - Emphasis on early phase development programs.
- Research and Development formulation and analytical, process chemistry for pre-FIH, Phase 1 program management of drug substance and drug product development projects.
- Project management experience (Scientific background is an absolute plus and prefer a scientist with experience in managing projects over a project manager without a scientific background.
- Pharmaceutical experience
- MS office
- MS Project preferred
- Excellent soft skills (e.g. negotiating, communicating)
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holidayand Vacation Pay
- Relocation Assistance
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| | | CA | S San Francisco | Permanent | Clinical Management | 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 TitlePosition Description- Key Representative of Company to the NIH
Position Responsibilities- Support the development and implementation of key projects.
- Generate and implement project timelines. Track and report progress using templates developed in conjunction with Sr. Management
- Manage and coordinate activities associated with the NIH
- Generation, development and review of key documents
- Oversight of 3 Coordinators
Position Requirements- PhD in Organic Chemistry highly preferred, or Biologist with strong Project Management and goverment contract experience.
- Experience will small molecules
- Experience with working with the NIH
- Previous leadership experience is a plus
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 | Clinical Management | 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
- Clinical Services Manager
Position Description - THIS POSITION IS HOME-BASED and located in the UK and WESTERN-Europe, and will most likely branch into Switzerland.
Position Responsibilities - Manage, maintain and serve as primary contact for existing customer relationships
- Develop and execute on account strategies, including, but not limited to the following
- Identify/confirm the customer’s business needs/drivers
- Identify other potential users (ex. expansion opportunities)
- Identify potential inside competition (ex. systems, initiatives, dissenters, re-organizations)
- Identify consult needs and lead the delivery of Study Consult Services (SCS) to customer
- Expand understanding and use of company’s software within existing customers, including customer’s Executive team
- Serve as lead on securing account expansion for Small and Mid Market accounts
- Support Sales Account Executive in expansion of Large and Global Accounts
- Identify new opportunities within existing customers (i.e. new products) and secure referrals to other opportunities
- Meet account objectives and quota for follow-on revenues
- Maintain strong relationships and satisfaction among existing customers
- Ensure continuation of licenses at contract renewal time
- Provide initial (BSO) training for all accounts
- Provide consult services as needed to meet customer needs and ensure software entrenchment in customer business processes
- Provide training support for accounts outside region as requested
- Provide advanced training with senior team members
- Act as Subject Matter Expert (SME) for sales opportunities when needed
- Lead trial/evaluation periods to secure final sale at mid-market accounts; may lead or assist senior team members in trial/evaluation exercises with major accounts
- Provide Sales and Marketing with feedback regarding new or existing market sectors that promote the adoption of the software
- Participate in, or moderate, speaking events and panel discussions at industry events
- Gather and provide feedback from customers and prospects to the product management group
- Act as a Subject Matter Expert (SME) for product enhancement, improvement and new product development
- Stay current with industry trends and best practices to ensure that ClearTrial products include relevant aspects for the customer (thought leadership)
Position Requirements - 5+ years experience in clinical operations, clinical trial project management, clinical trial costing, and/or clinical outsourcing/contract negotiation
- Strong entrepreneurial drive and ability to deliver results with limited supervision
- High energy, self-motivated, assertive; consummate professional
- Good customer presence and presentation skills
- Able to understand/analyze customers [unstated] needs
- Bachelors Degree or equivalent
- 2+ years as a business development professional selling into clinical operations departments of pharmaceutical/biotech companies; business development with a major CRO a plus
- 1+ years software sales experience in an enterprise software sales environment
- Strong technical, software acumen and abilities
- Background in solution selling
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 | Clinical Management | 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- Works with the Manager, Clinical Operations, the Clinical Research Manager II and other members of the clinical project team to ensure the execution of assigned clinical trials in accordance with Clinical Operations Plans.
Position Responsibilities- Trains and provides oversight to CRA teams including TCR and trip report review, co-monitoring and mentoring.
- Convenes and leads the cross-functional, matrix clinical study team(s) in the planning and execution of clinical trials in accordance with regulatory requirements and standard operating procedures.
- Participates in vendor management and vendor budget oversight.
- Plans, convenes, runs and presents at investigator meetings.
- Contributes to protocol concept, template Informed Consent Form and final protocol development.
- Coordinates and provides oversight to site contracting process.
- Conducts budget negotiations with sites.
- Provides input to patient recruitment strategies and operational feasibility and implementation of clinical trial objectives.
- Creates and implements study monitoring plans.
- Conducts on-site monitoring and performs site management for assigned sites.
- Prepares and ensures the accuracy and appropriateness of study-related reports, manuals and other tools.
- Coordinates ongoing study team review of clinical trial data
Position Requirements- BS/RN/RPh degree with 5+ years or MS degree with 3+ years of clinical operations experience including 1+ year of independent site monitoring/management 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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| | | NJ | Plainsboro | Temporary | Clinical Management | 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
· Oncology Project manager
Position Description
- Project manager of oncology clinical trials in the US, primarily investigator initiated studies or grants
Position Responsibilities - Position entails the review, management, and conduct of clinical trials.
- Inclusive of concept review, contracting, financial management, drug supply, regulatory, study closure and publication.
- The individual will be an active participant in product specific clinical strategic teams and other cross functional teams as necessary.
- Will interface with internal and external stakeholders and research organizations to facilitate the appropriate conduct of clinical trials.
Position Requirements - R.N., Pharm. D., Ph.D., M.D. A B.S. or M.S. will be considered if candidate has extensive experience in oncology clinical trial management and reporting.
- Highly organized and motivated, with ability to multi task and communicated directly. Management experience in the development and conduct of clinical trials, including budget negotiations, preferred.
- Must demonstrate the ability to work effectively across a matrix organization and have experience working in a dynamic team environment.
- Broad medical knowledge with experience in oncology preferred.
- Excellent communication and presentation skills both verbal and written.
Benefits · Blue Cross/Blue Shield Medical and Vision · Delta Dental · 401K with Company Match · Holidayand Vacation Pay · Relocation Assistance
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| | | NJ | Kenilworth | Temporary | Clinical Management | 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
- We are seeking to fill a contract position through Dec. 31, 2009, with the possibility of a 6 month extension, for a Project Physician in our client's Central Nervous System group.
- This is an immediate need and they are looking to bring someone on board ASAP.
Position Responsibilities - Lead clinical expert for Parkinson's drug development including Key Opinion Leader (KOL) contacts, meetings, field literature reviews
- Active input to clinical development team and other teams
- Site, Principal Investigator and other preparation for study start
- Operational critique of development of design, scales and global feasibility
- Participate in diverse CNS drug development from MS, pain, and movement disorders
- Execution of other functions as requested by management.
Position Requirements - The physician should have experience in Neurology, preferably industry or academic clinical trial experience with a focus on Parkinson's Disease.
- MD or PhD
Benefits - Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | NJ | Kenilworth | Temporary | Clinical Management | 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 Responsibilities
- The Project Physician will design, implement, and monitor studies (with a focus on Oncology) and interact with leading investigators in the field, to ensure the ethical and scientific basis of the study.
- Review and interpret data gathered. Identify and institute corrective measures when applicable.
- Ascertain any significant adverse reactions and closely monitor efficacy parameters.
- Assist in the dissemination of important scientific information through the writing/assisting in the writing of publications, abstracts and/or presentations.
- Also will be involved with due diligence of in-licensing opportunities.
Position Requirements MD from an accredited institution. ABIM Board certified (or Board eligible) with 0 to 3 years relevant experience in the US pharmaceutical or biotech industry. For those candidates not having industry experience, prior clinical trial experience and academic fellowship is preferred. Demonstrated excellence in oral, written communications. Ability to oversee and direct multiple projects with varying complexity involving multiple skill levels of subordinates with minimal assistance from supervisor - Benefits
- Blue Cross/Blue Shield Medical and Vision
- Delta Dental
- 401K with Company Match
- Holiday and Vacation Pay
- Relocation Assistance
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| | | PA | Exton | Permanent | Clinical Management | 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- A Pharmaceutical Project Management Generalist that understanding the process from concept through development.
Position Responsibilities
- Manage key documents relating to milestones
- Evaluate project progress against established timelines and evaluate the impact of key functional milestones on the overall timeline.
Facilitate the team in identifying rate limiting milestones, examining potential operational issues/risk, outlining those solutions and the trade-offs from a timeline, resources, quality and outcomes perspective, proposing multiple solutions, and identifying mitigation actions
Position Requirements - BA/BS minimum, MS and PMP certification preferred.
- 4-6 years relevant experience in pharmaceutical, biotechnology industry.
- Broad understanding of biotech/pharmaceutical product development from initiation to NDA approval.
- Ability to work semi-autonomously with strong organizational, prioritization and analytical skills.
- Ability to apply good judgment and facilitate problem solving within the team.
- Strong verbal, written and interpersonal skills
- Biologics experience
- Supply Chain experience
- Manufacturing 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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