Nation Wide Clinical Research Openings

[Guest guest]

Subject: Nation Wide Clinical Research Openings

Good afternoon,

What would you do if I could offer you a career involving life-saving

medicines? An experience of a lifetime? Take a look at what I have to

offer to someone who is familiar with Clinical Research. We are

looking for someone who is professional and willing to learn from an

experienced company. Take a look and tell me what you think.

Clinical Research Openings:

Philadelphia Area: 2 positions available.

1. Senior CRA - Any therapeutic area. Needing 2+ years industry

experience monitoring.

North Jersey area: 11 openings available.

1- Manager Oncology (contract). 5+ years pharma experience. Solid

Oncology experience. Candidate will be planning, managing , and

implementing clinical trial activities. overseeing inventory, training

Sr. CRA's, liaises and managing CRO's and conducting study team

meetings. RN or Masters strongly preferred.

2- Associate Director Clinical Operations -TRIC

3- Sr. Manager Clinical Operations Oncology. Responsible for leading

multi teams and studies within Oncology dept. CRO monitoring. Advanced

degree highly preferred. Experience tracking enrollment, budgets,

invoices, and monitoring reports. 7-10 years pharma experience

including line management experience. Masters, PhD or RN degree highly

preferred. Knowledge of entire drug development process. Detailed

knowledge of Code of Federal Regulations (CFRs) along with demonstrated

ability to manage and coach reports.

4- Associate Director/Director Clinical Operations Oncology... 3

positions available. Responsible for leading multiple teams and studies

within Oncology department. CRO monitoring. Advance degree highly

preferred. 10+ years of broad pharmaceutical industry experience

including line management experience required. Sound knowledge of drug

development process. Code of Federal Regulations (CFR's), ICH

Guidelines, Project and Data management along with Corporate and

Regional SOPs.

5- Sr. Director Clinical Operations. Must have experience budgeting

department funds. Candidate will be responsible for managing and

developing a team of direct reports. (MS) Advanced degree highly

preferred. 10-12 years relevant pharmaceutical industry experience

required. NDA and Advisory Board (pl-3 study) preparation experience

needed.

6- Manager of Clinical Operations. Responsible for leading multiple

teams and studies within Oncology department. CRO monitoring. Advanced

degree highly preferred. Experience tracking enrollment, budgets,

invoices, and monitoring reports. 5-8 years experience including line

management experience. Masters, Ph

D, or RN degree highly preferred. Knowledge of entire drug development

process.

7- Sr. CRA Oncology (contract) - 2-5 years management. Global

experience a big plus. Experience with tracking enrollment, budget/

invoices, monitoring reports, data collections, holding and attending

study team meetings.

8-Senior CRA ACCESS Study (Sepsis) perm. - Any therapeutic area. Must

have 5-7 years CRA experience in the pharmaceutical industry. 7+ if

they only have CRO experience. Needs a minimum of a BA. Nursing

degree with critical care experience is a big plus though no longer

necessary. Patient enrollment and date review a must. Solid CRA

experience with some monitoring. All monitoring experience will not

qualify. No specific TA required. Global exp. managing CRA's and

CRO/Vendors in BIG> Position can move up to Associate manager or

Manager position for the right candidate. SOLID research experience.

9- Sr. CRA Sepsis (contract) - Strong data review, patient profiling,

CRO management. Need solid CRA experience coming out of pharma or a

CRO.

10- Contract Associate Manager/Manager-Clinical operations, Oncology

Description:

To manage the following Oncology studies: E7389 A001 104 and E7389 A001

202, Assist on panning, managing, and implementing clinical trial

activities, specifically, building external CRO's, vendor relationships,

managing approved study timeline. Prepares, reviews, and finalizes

documentation of site visits identifying progress to-date, and outlining

study implications for EGC.

Developes and delivers reports/status updates to internal team, study

team, and CRO. Oversee product inventory during clinical trial process

and projects/models the clinical supplies required to conduct additional

clinical test (laboratory supplies, case report form book, etc.)

Accesses, analyzes and proactively develops corrective acton plans for

difficult investigational sites, vendors, and administrative issues.

Trains and guides Associates and Sr. CRA's. Coordinates, communicates

with sites and co-monitors in accordance with ICH/GCP guidelines and EMR

SOP's/WPs. Liaises with and manages CRO's, manages Technical Service

Providers (TSP). Reviews and tracts enrollment, budget/invoices,

monitoring reports, coordinates data collection, provides study

projections and updates to the team. To hold and attend study team

meetings, including CRO vendor and site meetings.

Qualifications:

Pharmaceutical industry experience required. Oncology experience

required. 5+ years pharma experience with clinical research experience.

Experience handling multiple tasks. Strong personnel management

experience required. Bachelor's degree required in associated

scientific discipline; RN pr Master's degree strongly preferred.

Scientific background with understanding of clinical development and

drug development process together with a broad understanding and

experience of clinical operations. Technical capabilities to lead small

or multiple clinical studies from protocol development to final analysis

and submission. Strong verbal written and interpersonal communication

skills especially relationship management with ability to give/receive

feedback ad build consensus.

11- Contract Sr. CRA-Clinical Operations Oncology

Description:

Basic understanding of clinical study process, with specialized

technical skills to deliver own work with the clinical study team;

ability to work semi-autonomously with strong organizational,

prioritization and analytical skills. Liasies with CRO's vendors and

third parties to the clinical study. Review and track enrollment,

budget/invoices, monitoring reports, coordinate data collection, provide

study projections and updates to the team, hold/attend study team

meetings. Undertake overall management, coordination, co-monitoring of

clinical study according to EMR SOPs/WPs; and to ensure quality of data

from such sites are acceptable and suitable for regulatory submission.

To assist and work in the clinical operations of E7389 G000 211 study.

Qualifications:

Pharmaceutical industry or CRO experience required. MUST have minimum

of 1 year current Oncology experience. Minimum of a college degree in a

relevant scientific discipline. 2-5 years experience in study

management, clinical monitoring, site coordination experience in the US.

Global experience highly desirable. Full understanding of current

ICH/GCP guidelines.

Thanks for your time.

Riley

Office Manager

Pharma-Search Partner Inc

Riley@...

Riley

President

Pharma-SearchPartners Inc