Job Title: Drug Development Scholar
Company: Scottsdale Healthcare
Location: Scottsdale, AZ
Description:
Discover a place where personalized care and personalized careers come together in a spectacular location. At Scottsdale Healthcare, treating our patients and our staff as the unique individuals they are is more than our mission -- it is our passion. Job Details: Functions as a specialist physician in performing duties involving direct care of patients with advanced malignancies receiving treatment on clinical trials. Evaluates new patients and formulates treatment plan under supervision of the assigned faculty member. The level of direction and guidance received from the assigned faculty member varies according to the individual's knowledge, skill and years of experience, as determined by the assigned faculty member. The TCRS Drug Development Scholar Program provides two years of intense training that will include clinical trials development, patient recruitment and follow up, statistical analysis, bioinformatics and regulatory affairs. The Drug Development Scholar is expected to abide by all hospital and Medical Staff policies and procedures and participate fully in the educational activities of the Drug Development Scholar Program. Staff member must demonstrate knowledge of internal medicine and hematology/oncology and demonstrate the skills necessary to provide direct and indirect care appropriate to the needs of patients admitted on his/her assigned unit. The individual must posses the ability to assess each patient's requirements relative to his/her medical and age-specific needs and to provide the care needed as described in the Department Operating Policies. Basic Education Knowledge of medicine as acquired through completion of a doctoral degree in medicine from an approved program. Completion of a postgraduate training program in Internal Medicine and Medical Oncology with added qualifications in Medical Oncology and or hematology Eligible for a medical license or Institutional Permit issued by the AZ Medical Board We will provide you with professional benefits tailored to your unique needs. Benefits such as: Medical and dental benefits that start day one PTO 403 (b) retirement plan Degree completion & advanced degree programs Sick child care & elder care programsScottsdale Healthcare fosters a collaborative culture that has been recognized by The Business Journal of Phoenix as one of the Best Places to Work in the Valley 2005. Away from work, you'll find that Scottsdale offers a richly satisfying lifestyle with breathtaking sunsets, year-round outdoor recreation and 300 days of sunshine and blue skies.Apply Here EOE/AA
Job Title: CRA-Phase II & III Drug Development-Princeton Area Pharmaceutical Company
Company: Cornerstone Search Group, LLC
Location: Princeton, NJ
Description:
CRA-Phase II & III Drug Development-Princeton Area Pharmaceutical Company
Summary: Great opportunity to join a very successful & profitable Princeton, NJ area Pharmaceutical Company that has multiple approved FDA drugs and a rich development pipeline.
Company Description: A highly successful and profitable Princeton, NJ area Pharmaceutical Company with multiple FDA approved drugs and deep development pipeline.
Location: Princeton, New Jersey areaCompensation: Compensation will vary depending upon the depth and quality of relevant clinical operations experience. The base salary can be in the $65k to $75k range, and this position is also eligible for an annual and a very extensive benefits package (401k, pension plan, flexible workday starting and ending times, summer hours, week between Xmas and NY’s Day off and more)
Attractive features about this opportunity/position and company:
Great opportunity to join a financially successful and strong company.
Chance to join a company with a strong development pipeline (and future prospects)
Company offers an extensive and great benefits package
Join a very talented team of experienced pharmaceutical professionals that you can learn a lot form and with.
Company offers a very pleasant and enjoyable work environment.
Responsibilities:
In a nutshell, you will work closely with Clinical Study Managers and Sr. CRAs to perform a broad range of in-house and field-based clinical operations activities for multiple drugs in Phase II and/or Phase III stages of clinical development.
Requirements:
Education: BA/BS (a life sciences degree is preferred)
Three (3) or years of Clinical Operations experience gained working in industry for a pharmaceutical/biotechnology company and/or CRO.
Hands-on site monitoring experience and clinical documentation review and analysis experience.
The willingness to travel up to 30% to 50% at times as necessary (note: this is not meant to be a monitoring position, however, there is travel involved as necessary with investigator meetings, site study start-ups, visiting problem sites, visiting sites with CRO monitors…)
Cornerstone’s Privacy Policy
Cornerstone Search Group considers all inquiries, resume submissions, and any other personal information submitted to us as confidential information. This information will not to be shared with any parties outside of Cornerstone Search Group without your prior permission.
Contact:
Cliff Miras (initial contact via email is preferred)
Co-founder & Managing Partner
Cornerstone Search Group, LLC
6 Campus Drive
Parsippany, NJ 07054
P Register to View ext 711
F Register to View
Email Cliff Miras: Register to View
Web/URL: www.cornerstonesg.com
About Cornerstone Search Group, LLC
Cornerstone Search Group is a Specialized Pharmaceutical | Biotechnology Executive Search & Recruitment Firm located in Parsippany, NJ. Cornerstone helps its Pharmaceutical | Biotechnology clients find, attract and hire accomplished professionals from the experienced Staff Levels (e.g. Managers/Sr. Managers) through the Sr. Leadership ranks (e.g. Directors, Sr. Directors, Executive Directors, VPs, Sr. VPs and EVPs) involved with the discovery, development and commercialization of drugs/therapeutic treatments for the US and international markets.
Keywords
CRA, Clinical Research Associate, Lead CRA, Clinical Trials, Clinical Studies, FDA, NDA, IND, investigational, Principal Investigator, AE, SAE, Clinical Study Report, Clinical Summaries, Patient Narratives, Medical Director, CRF, ICF, protocol, IRB, IB, Investigator Brochure, Investigator Meeting, Internal Review Board, Informed Consent Form, Case Report Form, monitoring, Adverse Event, Serious Adverse Event
Job Title: Outsourcing Manager - Drug Development
Company: PharmaceuticalCrossing
Location: Summit, NJ
Description:
Outsourcing Manager - Drug DevelopmentResponsibilities:
Perform and manage all activities associated with the development and execution of contracts with non-clinical early drug development contract research organizations and other vendors as necessary.
Prepare study specific request for proposals.
negotiations, benchmarking and sourcing strategy.
Prepare contracts, negotiate any requested changes to wording, identifying changes to the Legal department and coordinate any changes requested in areas of the contract.
Track, manage and monitor all changes to study scope ensuring timely change order finalization and implementation.Requirement:
A BA/BS degree in life sciences, business, finance is required.
A MBA/MS a plus.
4 years in the Pharmaceutical Industry.
2 years of in outsourcing early drug development services including outsourcing animal toxicology studies and DMPK.
Advanced knowledge of contract terms and conditions.
Advanced knowledge of benchmarking, market analyses and financial negotiations.
Advanced problem solving skills in a team environment.
Excellent negotiation/influencing skills.
Proficient in early drug development process.
Competent in computer skills & multi-tasking.
Ability to manage personal timelines provide input to support staff timelines.For further information, please visit us online at http://www.pharmaceuticalcrossing.com Please send your resume to PharmaceuticalCrossing at Register to View Apply Now
There will be charge of $29.95 per month (or a lower monthly rate based on agreement length) after your 7 day FREE Trial to use our service.
Job Title: Sr. CRA (in-house)-Phase II & III Drug Development-Princeton Area Pharma Co
Company: Cornerstone Search Group, LLC
Location: Princeton, NJ
Description:
Sr. CRA (in-house)-Phase II & III Drug Development-Princeton Area Pharma Co
Summary: Great opportunity to join a very successful & profitable pharmaceutical company with a deep development pipeline to develop new drugs/treatments.
Company Description: A highly successful and profitable established Princeton, NJ area Pharmaceutical Company with a strong development pipeline.
Location: Princeton, New Jersey areaCompensation: Compensation will vary depending upon the depth and quality of relevant clinical operations experience. The base salary can be in the $75k to $85k range (maybe higher depending upon experience), and this position is also eligible for an annual bonus (note: total compensation (i.e. base salary, bonus, 401k company contributions and more) can approximate or exceed $100k. This company’s also offers an extensive benefits package (e.g. pension plan, week between Xmas and NY’s Day off in addition to vacation time, flexible workday starting and ending times and much more)
Attractive features about this opportunity/position and company:
Great opportunity to join a financially successful and strong company.
Chance to join a company with a strong development pipeline (and future prospects)
Company offers an extensive and great benefits package
Join a very talented team of experienced pharmaceutical professionals that you can learn a lot form and with.
Position is open due to promotion—the company offers an attractive opportunity to advance over time.
Company offers a very pleasant and enjoyable work environment.
Responsibilities:
In a nutshell, you will be responsible for Sr. CRA in-house responsibilities, which include but are not limited to performing the following: interacting with study site personnel regarding questions they have about protocols (e.g. patient qualification), CRF forms, clinical data, study supplies and more, leading/directing/reviewing work performed by internal CRAs and external CRAs working for CROs, reviewing clinical data collected on an ongoing basis, identifying potential problems/issues and resolving them (e.g. missing data, site visit report issues identified) and more.
Requirements:
Education: BA/BS (a life sciences degree is preferred)
2- 5 or years of Clinical Operations experience gained working in industry for a pharmaceutical/biotechnology company and/or CRO.
Clinical Operations experience to include directing/leading/reviewing the work performed by staff level CRAs, hands-on site monitoring experience (current or in the past), interacting with investigational site personnel regarding their protocols, clinical data, clinical supplies…
The willingness to travel up to 25% if necessary (note: this is not a monitoring position, however, there is some travel involved as necessary with investigator meetings, site study start-ups, visiting problem sites…
Cornerstone’s Privacy Policy
Cornerstone Search Group considers all inquiries, resume submissions, and any other personal information submitted to us as confidential information. This information will not to be shared with any parties outside of Cornerstone Search Group without your prior permission.
Contact:
Cliff Miras (initial contact via email is preferred)
Co-founder & Managing Partner
Cornerstone Search Group, LLC
6 Campus Drive
Parsippany, NJ 07054
P Register to View ext 711
F Register to View
Email Cliff Miras: Register to View
Web/URL: www.cornerstonesg.com
About Cornerstone Search Group, LLC
Cornerstone Search Group is a Specialized Pharmaceutical | Biotechnology Executive Search & Recruitment Firm located in Parsippany, NJ. Cornerstone helps its Pharmaceutical | Biotechnology clients find, attract and hire accomplished professionals from the experienced Staff Levels (e.g. Managers/Sr. Managers) through the Sr. Leadership ranks (e.g. Directors, Sr. Directors, Executive Directors, VPs, Sr. VPs and EVPs) involved with the discovery, development and commercialization of drugs/therapeutic treatments for the US and international markets.
Keywords
Sr. CRA, Senior Clinical Research Associate, Lead CRA, Sr. CRA, Senior CRA, Clinical Trials, Clinical Studies, FDA, NDA, IND, investigational, Principal Investigator, AE, SAE, Clinical Study Report, Clinical Summaries, Patient Narratives, Medical Director, CRF, ICF, protocol, IRB, IB, Investigator Brochure, Investigator Meeting, Internal Review Board, Informed Consent Form, Case Report Form, monitoring, Adverse Event, Serious Adverse Event
Job Title: Drug Development Scholar
Company: Scottsdale Healthcare
Location: Phoenix, AZ
Description:
Drug Development Scholar (307651)
- Full-Time - M-F 8:00am - 4:30 pm
- Days
Functions as a specialist physician in performing duties involving direct care of patients with advanced malignancies receiving treatment on clinical trials. Evaluates new patients and formulates treatment plan under supervision of the assigned faculty member. The level of direction and guidance received from the assigned faculty member varies according to the individual's knowledge, skill and years of experience, as determined by the assigned faculty member.
The TCRS Drug Development Scholar Program provides two years of intense training that will include clinical trials development, patient recruitment and follow up, statistical analysis, bioinformatics and regulatory affairs. The Drug Development Scholar is expected to abide by all hospital and Medical Staff policies and procedures and participate fully in the educational activities of the Drug Development Scholar Program.
Staff member must demonstrate knowledge of internal medicine and hematology/oncology and demonstrate the skills necessary to provide direct and indirect care appropriate
to the needs of patients admitted on his/her assigned unit. The individual must posses the ability
to assess each patient's requirements relative to his/her medical and age-specific needs and to provide the care needed as described in the Department Operating Policies.
Job Requirements
Basic Education
Knowledge of medicine as acquired through completion of a doctoral degree in medicine from an approved program.
Completion of a postgraduate training program in Internal Medicine and Medical Oncology with added qualifications in Medical Oncology and or hematology
Job Title: Outsourcing Manager - Drug Development
Company: SciencesCrossing
Location: Summit, NJ
Description:
Outsourcing Manager - Drug DevelopmentResponsibilities:
Perform and manage all activities associated with the development and execution of contracts with non-clinical early drug development contract research organizations and other vendors as necessary.
Prepare study specific request for proposals.
negotiations, benchmarking and sourcing strategy.
Prepare contracts, negotiate any requested changes to wording, identifying changes to the Legal department and coordinate any changes requested in areas of the contract.
Track, manage and monitor all changes to study scope ensuring timely change order finalization and implementation.Requirement:
A BA/BS degree in life sciences, business, finance is required.
A MBA/MS a plus.
4 years in the Pharmaceutical Industry.
2 years of in outsourcing early drug development services including outsourcing animal toxicology studies and DMPK.
Advanced knowledge of contract terms and conditions.
Advanced knowledge of benchmarking, market analyses and financial negotiations.
Advanced problem solving skills in a team environment.
Excellent negotiation/influencing skills.
Proficient in early drug development process.
Competent in computer skills & multi-tasking.
Ability to manage personal timelines provide input to support staff timelines.For further information, please visit us online at http://www.sciencescrossing.com Please send your resume to SciencesCrossing at Register to View Apply Now
There will be charge of $29.95 per month (or a lower monthly rate based on agreement length) after your 7 day FREE Trial to use our service.