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Rose Chu's Jobs

RAVE Project Manager

RAVE Project Manager - manage the Medidata RAVE implementation and migration process for a well-known Clinical company located in Philadelphia, PA. Forward resume to rchu@gesnetwork.com for discussion

RAVE Project Manager Job Description We are currently seeking a Project Manager/Administrator II to manager the Medidata RAVE implementation and migration process for our top clinical client. Summary: Looking for ...

Philadelphia, PA

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Home-based Contract West Coast CRA

Home-based with LOCAL travel to 10 sites in LA; 100% Hourly work/paid- Interested? Regional opportunity - if you know what we are looking for, then we need to talk ASAP. Pls forward CV to rchu@gesnetwork.com or call #610-822-1256. Call/email CV NOW!

We have 10 sites in L.A. areas and looking to hire a Regional CRA with 100% availability ASAP. This is a contract or contract-to-perm opportunity with a Global Clinical Company ...

Los Angeles, CA

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Biostatistician/Statistician

5 years pharmaceutical Biostat/Stat experience - please send resume to rchu@gesnetwork.com. EXCELLENT COMPENSATION!! MARKET RATE!

a Pharmaceutical company in the Princeton, NJ area, who is currently searching for a Biostatistician/Statistician with Ph.D or Masters Degree in Statistics or Biostatistics and at least 5 year experience ...

Princeton, NJ

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Sr. GMP Validation Specialist

A biopharmaceutical company is looking for a Senior Validation Specialist, Pilot Plant with 5-7 years of relevant validation experience in a biopharmaceutical/cGMP environment. please send resume to rchu@gesnetwork.com

A biopharmaceutical company is looking for a Senior Validation Specialist, Pilot Plant with 5-7 years of relevant validation experience in a biopharmaceutical/cGMP environment. Job description and requirements below: Senior Validation ...

Exton, PA

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Drug Safety Physician

drug safety Physician with 3-5 years pharma industry experience and NDA filing. ARGUS/ARISg. send resume to rchu@gesnetwork.com

Are you a MD or BSN with pharmaceutical industry Drug Safety experience within ARGUS or ARISg? If you possess at least 3 years experience with pharmaceutical industry and looking for ...

Princeton, NJ

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Senior Biostatistician

Senior Biostatistician in DC/MD/VA areas - Master level Biostatistician with 5+ year pharmaceutical experiences; programming experiences; SAP development experience required. Pay up to $85+/hr. Send resume to rchu@gesnetwork.com for discussion.

Industry: Pharmaceutical, Biotechnology Job Title: Senior Biostatistician Job Type: Pharmaceutical, Biotech Required Education: Graduate Degree Required Experience: 5 to 10 years Required Travel: None Relocation Covered: Not Specified Location: DC/VA/MD ...

Rockville, MD

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Senior Statistical Programmer

Sr. Statistical Programmer -MS in Statistic with 10+ yrs pharma industry SAS programming experience, strong statistical experience, strong programming exp in clinical trials and NDA filing. Pay $60 to $100/hr. Please send resume to rchu@gesnetwork.com

Senior Statistical Programmer Job Description If you have MS in Statistic and 10+ years experience in SAS programming experience in clinical trials and strong CDISC experience, please apply for interview ...

Parsippany, NJ

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Oncology Project Manager

CPM - multiple oncology trials. $60 to $85/hr Please forward resume to rchu@gesnetwork.com for discussion.

Requirement for Clinical Project Manager – Oncology Trials Bachelor’s degree preferred; RN or Associate Degree in an allied health profession with appropriate experience may be considered. Knowledge of broad clinical ...

Philadelphia, PA

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Sr. CRA/Clinical Project Manager/Regional Lead

Sr. CRA/Clinical Project Manager/Regional Lead - less than 25% travel, 3-5 days on site - please email Rose Chu at rchu@gesnetwork.com for details.

A Global Pharmaceutical company located in Rockville, MD, who are in need of a Regional Lead, Company requires for minimum 5+ years pharmaceutical industry with previous experience as a Sr. ...

Rockville, MD

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Sr. CDA/ Clinical Data Management

Sr. CDA/CDM/CDC - Lead CDM and Lead CDA. Prefer RAVE experience. Please call 610-822-1256 for details or email resume for response!

Sr. CDA opportunities - please forward resume to rchu@gesnetwork.com for review. Major Duties and Responsibilities: Follows established GCP procedures and practices for implementing and maintaining processes to assure departmental goals ...

Philadelphia, PA

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Sr. Regulatory Affairs Associate/Manager

Sr. Reg. Affairs Associte/Manager - 5 yrs MIN of NDA experience (wants someone that knows the ins and out. Develop, write, review etc) - forward resume to rchu@gesnetwork.com or call Rose Chu at 610-822-1256. IMMEDIATE RESPONSE!! INTERVIEW THIS WEEK!

A fast-growing consumer products company in the Langhorne, PA area, who is currently searching for a Sr. Regulatory Affairs Associate/Manager. Sr. Regulatory Affairs Associate/Manager needs to have direct experience investigating, ...

Langhorne, PA

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Sr. Validation Clinical SAS Programmer

Sr. Validation Clinical SAS Programmer - proficient in SAS Programming validation of Analysis data sets, SDTMs,Tables and Listings.CDISC/SDTM/AdAM standards. 5+ years IN PHARMA INDUSTRY required. Please send resume to rchu@gesnetwork.com for discussion

If you have 5+ years experience in SAS programming experience in clinical trials and strong Validation/CDISC experience, please apply for interview within 24 hours. We are only interested in candidates ...

Rockville, MD

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Senior Clinical Data Manager/CDM

Sr. CDM/CDM - one day work from home, 4 days flex time. Please send resume to rchu@gesnetwork.com for discussion.

or over 30 years the GES Pharmaceutical Division has placed a full range of entry-to-director-level position in companies that service the Pharmaceutical, Biotech and Medical Device industry. If you are ...

Philadelphia, PA

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Biostatistician - pharmaceutical experience required

Biostat and Clinical SAS Programmer openings - long-term contract. On site in Rockville, MD with some flexibility. Please contact Rose at #610-822-1256 for details.

Job Description If you have Master level in Statistics or Biostatistics with at least 2 years pharmaceutical company/CRO experience, please apply NOW for an interview within 24 hours. We are ...

Rockville, MD

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Clinical Project Coordinator

Excellent Clinical Project Administrator opportunity in Princeton, NJ. Please call Rose Chu at 610-822-1256 or email rchu@gesnetwork.com for details

Global Pharmaceutical company is looking for a Clinical Project Coordinator/Administrator to join their CNS group. 3-5 years pharmaceutical industry experience required. TASKS & RESPONSIBILITIES: Assists in maintenance, quality control, distribution, ...

Philadelphia, PA

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Clinical Trials Associate

Clinical Trials Associate Provide general study administrative support including, but not limited to: Assist in clinical study set-up for administrative and logistical tasks, including preparation and/or submission of IEC/HA files ...

Cherry Hill, NJ

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Sr. Regulatory Liaison

A leading biopharmaceutical company in the Exton, PA area, who is in need of a Senior Regulatory Liaison. Sr. Regulatory Liaison provides global oversight, direction and leadership for all regulatory ...

Philadelphia, PA

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Clinical Trials Project Specialist II

Clinical Trials Project Specialist II A clinical research division in Philadelphia has been the leading research organization for over 500 research studies. As a member of the team you will: ...

Philadelphia, PA

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Protocol Associate

Contract Protocol Associate, Protocol Development and Regulatory Compliance, Diagnostic Imaging Duties Include: Edits and proofreads protocol documents for required format and requisite content Manages assigned protocols Interacts with protocol chairs ...

Philadelphia, PA

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Job Title In-House Clinical Research Associate Manager’s Job Title Director, Clinical Operations Division/Department Clinical Operations Job Summary Provides support to clinical operations team in planning, conduct, and closeout of assigned ...

Philadelphia, PA

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