Rose Chu's Jobs
Clinical Supply Manager
Clinical Supply Management opportunity - $60 to $120/hr. Please send your CV to rchu@gesnetwork or call Rose Chu at #610-822-1256 for discussion
Clinical Supply Manager The Clinical Supply Manager (CSM) is primarily responsible for providing support to the Chemistry, Manufacturing and Control (CMC) Team to ensure clinical supplies are packaged, labeled, and ...
Clinical Safety Data Entry Specialist
Global Biopharmaceuitcal company is look for a Clinical Safety Data Entry Specialist - BS or RN with 2 years Pharmaceutical industry safety data entry (ARGUS). Please send CV to firstname.lastname@example.org
Clinical Safety Data Entry Specialist Job Description A leading global biopharmaceutical company is looking for a strong Clinical Safety Data Entry Specialist. If you are have Bachelor degree in a ...
Pharmaceutical Validation Analyst
Active search for Pharmaceutical Validation Analyst requires 5+ years in computer systems validation/QA (Pharmaceutical industry required) with good understanding of cGxP (cGMP, cGDP, cGAMP, cGLP). Please send resume to email@example.com
A leading global pharmaceutical is looking for a Supply Chain Validation Analyst to support testing and validation activities for Global Supply Chain information systems. Primary responsibilities include validation support for ...
Chesterbrook, PAlearn more
Sr. Clinical SAS Programmer
LONG-TERM (1-3 years) contract. Looking for 8+ years Clinical SAS with Strong Submissions exp(NDAs etc to FDA and / or European agency) and Skills in CDISC/SDTM/ADAM. $75/hr or more. Please forward resume to firstname.lastname@example.org for discussion.
SR. CLINICAL SAS PROGRAMMER Job Description If you have 8+ years experience in SAS programming experience in clinical trials and strong CDISC experience, please apply for interview within 24 hours. ...
Washington, DClearn more
Sr. Drug Safety Associate
Sr. Drug Safety Associate - 5 years industry drug safety with NDA filing experience and skills in ARGUS/ARISg. Please call (610.822.1256) or forward your CV/Resume to email@example.com for discussion.
Job Description Are you a Drug Safety professional who has previous working experience within ARGUS or ARISg? If you possess at least 5 years experience with pharmaceutical industry and looking ...
Are you interested in discussing the following? Please call Rose Chu at #610-822-1256 PhD or Pharm D or MS in Pharmacokinetics/Clinical Pharmacology preferred. 2 years of pharmaceutical industry experience in pharmacokinetics, clinical studies.
A Leading Global Biopharmaceutical Company is looking for Pharmacologist, Clinical Pharmacology to report to the Director of Clinical Pharmacology. Clinical Pharmacologist is responsible to provide Clinical Pharmacology input to all ...
Data Manager, Clinical Data Management
Data Manager - BA/BS with 8 to 10 solid Biopharmaceutical industry experience in Data Management.Proficient in EDC. Please forward resume to firstname.lastname@example.org for interview.
Data Manager, Clinical Data Management Address: Princeton, NJ 08540 Essential Functions: Oversee all aspects of data management tasks performed by vendor: Review and approve mock CRF and eCRF screen within ...
Biostat/Statistician - 3 to 5 years experience within Pharmaceutical industry. Please send resume to email@example.com for interview. Rose Chu 610-822-1256
Job description and requirements below: Accountable for statistical expertise to: • Strategic planning of the program • Statistical components of protocol that meet study objectives • Statistical component of reports ...
Clinical SAS Programmer
MS in Statistics and 4 years Pharma/CRO SAS programming experience. resume to firstname.lastname@example.org for other home-based opportunities.
Clinical SAS Programmer Job Description A leading Clinical Company has been providing services in areas including Dermatology, Cardiovascular, Respiratory, Allergy, Immunology, CNS and Oncology. We are looking for 2 SAS/Statistical ...
Wayne, PAlearn more
Global Regulatory Affairs Manager
Global Regulatory Affairs Manager with 5+ years regulatory affairs with oral solid dose, both small and large molecules. Global regulatory experience with Biologicals and Oncology a plus. Please send resume to email@example.com
Job Description At Global Employment Solutions, one of the top HR consulting and staffing services firm has been helping candidates achieve their career dreams and goals by hiring consultants to ...
Sr. Clinical Data Associate
Sr. CDA to managing the Data Mgmt processes with various CRO partners.6+ years of pharmaceutical industry experience in data cleaning/review in clinical trials or 9 years of data management experience. Send resume to firstname.lastname@example.org for discussion
Job Description Are you a CDM/CDA/CDC professional who has previous working experience with data cleaning/review in clinical trials? If you possess at least 6 years experience with pharmaceutical industry and ...
Rockville, MDlearn more
Clinical Data Associate
3 CDA opportunities for candidates with 3-5 years Pharmaceutical industry Clinical Data Associate/Coordinator experience. To get more details, please forward resume to email@example.com or call Rose Chu at #610-822-1256
Job Title: Clinical Data Analyst Summary: Perform review of CRFs and data discrepancy management of clinical trial data. Working to departmental SOPs, guidelines and global standards, maintain data integrity and ...
Medical Writer - Doctorate degree (PhD)/ Masters/ Bachelor’s Degree in Bio-Medical Science/Pharmacy or related field, 3-5 yrs Medical Degree with 1-4 years of Regulatory Writing experience. Please communicate through firstname.lastname@example.org
# of positions: 2 Pay Rate: open, please submit at the best rate possible. Start Date: ASAP Job Description: Doctorate degree (PhD)/ Masters/ Bachelor’s Degree in Bio-Medical Science/Pharmacy or related ...
Bridgewater, NJlearn more
Lead Clinical Data Manager
Sr. CDM opportunity in Northern NJ areas. To Lead and Manage project activities at Study level at assigned client sites for Clinical Data Management. Please communicate through email@example.com
# of positions: 4 to 6 Target Start Date: IMMEDIATELY REQUIRED: **Must have solid Data Management experience. **Must have solid Project Management experience. **Must be able to start immediately. Job ...
East Hanover, NJlearn more
Biostat/Stat needed in Northern, Central NJ areas or CT. Home-based opportunities in East Coast. Please communicate through firstname.lastname@example.org
# of positions: 6 Target Start Date: ASAP REQUIRED: •University degree (MSc, PhD) in Statistics, Mathematical Statistics or Biostatistics, or equivalent experience. •Comprehensive knowledge of Clinical Drug Development processes and ...
Bridgewater, NJlearn more
Biostat - Master or Ph.D in statistics or Biostatistics with 5 years pharma industry experience - pay $90/hr with flexibility Send resume to email@example.com for discussion
Biostatistician/Statistician Job Description Pharmaceutical companies in the DC/VA/MD/DE/PA areas, who are currently searching for multiple Biostatistician/Statistician/Sr. Statistical Programmer with Ph.D or Masters Degree in Statistics or Biostatistics and at least ...
Wilmington, DElearn more
Study Designer/EDC Programmer
looking for a Study Designer with strong EDC experience and build study or studies in RAVE or and EDC. Please apply firstname.lastname@example.org with your resume (word document) attached for discussion.
Study Designer/EDC Administrator Job Description A leading Clinical Research Company located in Philadelphia, PA, is looking for a Study Designer with strong EDC experience and build study or studies in ...
Sr. Statistical Programmer
If you are in the DE, MD, DC, VA areas and have 9+ years experience in SAS programming experience in clinical trials and strong CDISC experience, please apply email@example.com with your updated resume for phone interview within 24 hours.
If you are in the DE, MD, DC, VA areas and have 9+ years experience in SAS programming experience in clinical trials and strong CDISC experience, please apply for phone ...
Rockville, MDlearn more
Senior Complaince Manager, GxP
Sr. Compliance Manager - 5+ years of pharmaceutical industry compliance/GxP related documentation experience required. 3 to 4 years of project management experience preferred. Please forward resume to firstname.lastname@example.org for discussion
A leading Clinical Research Company located in Philadelphia, PA, is looking for a Senior Compliance Manager to provide managerial support to the Information Technology Department supporting the clinical research portfolio. ...
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 ...