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 email@example.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 ...
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 firstname.lastname@example.org 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, CAlearn more
5 years pharmaceutical Biostat/Stat experience - please send resume to email@example.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, NJlearn more
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 firstname.lastname@example.org
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, PAlearn more
Drug Safety Physician
drug safety Physician with 3-5 years pharma industry experience and NDA filing. ARGUS/ARISg. send resume to email@example.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, NJlearn more
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 firstname.lastname@example.org 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 ...
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 email@example.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, NJlearn more
Oncology Project Manager
CPM - multiple oncology trials. $60 to $85/hr Please forward resume to firstname.lastname@example.org 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 ...
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 email@example.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. ...
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 firstname.lastname@example.org for review. Major Duties and Responsibilities: Follows established GCP procedures and practices for implementing and maintaining processes to assure departmental goals ...
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 email@example.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, PAlearn more
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 firstname.lastname@example.org 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 ...
Senior Clinical Data Manager/CDM
Sr. CDM/CDM - one day work from home, 4 days flex time. Please send resume to email@example.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 ...
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 ...
Clinical Project Coordinator
Excellent Clinical Project Administrator opportunity in Princeton, NJ. Please call Rose Chu at 610-822-1256 or email firstname.lastname@example.org 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, ...
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 ...