Global Employment Solutions, Inc.
Sr. Clinical Programmer, PK/TLF/SAS
HIRING Sr. Clinical Programmer in Greater Philadelphia with 6+ years clinical programming experience including PK TLF programming; strong SAS graph skills. Working 3 days from home after training. Up to $100/hr or more. CV to firstname.lastname@example.org
We are looking for a strong Clinical Programmer for a leading biopharmaceutical company. This position will have some flexibility of working from home 2-3 days/week after training. Excellent hourly rate ...
Exton, PAlearn more
GCP Compliance Specialist
GCP Compliance with 5 yrs of pharma industry GCP Compliance/auditing experience and TrackWise. Available to work onsite (Greater Philadelphia areas) with no travel. CV to email@example.com
A leading Biopharmaceutical company is looking for a GCP Compliance Specialist to monitor clinical studies to support a QC program where quality thresholds can be met or exceeded, and that ...
Sr. Scientific Communications Consultant, Regulatory Affairs
HIRING FOR a Sr. Scientific Communication Consultant - MS or MA + 7 years, PharmD or PhD plus 4 years of Pharmaceutical industry experience in Scientific Communications with medical writing experience. CV to firstname.lastname@example.org
Sr. Scientific Communications Consultant, Regulatory Affairs We are currently seeking a Sr. Scientific Communications Consultant to join the Regulatory Affairs team of a US Pharmaceutical company Sr. Scientific Communications Consultant ...
Aseptic Process Qualification Engineer
HIRING for Aseptic Process Qualification Engineer with pharmaceutical validation/microbiology experience and available to work in Ocean County/Hopewell, NJ. CV to email@example.com
The candidate will assume a critical role in a highly motivated group within a leading contract manufacturing facility supporting the qualification of aseptic processes (i.e. media simulation activities), bulk sterilization, ...
QUALITY ENGINEER - CLEANING VALIDATION
We are searching for Validation Engineer with years experience performing cleaning activities validation within a pharmaceutical environment.outlined by the FDA, ISO, EU and ICH. Resume to firstname.lastname@example.org
The candidate will assume a critical role in a highly motivated group within a leading contract manufacturing facility supporting the cleaning qualification / validation and filter validation activities associated with ...
Associate Biotech Scientist
Do you know any 2nd shift Associate Scientist to performs analytical testing of samples in a cGMP compliant manner to service manufacturing and production. CV to email@example.com
Performs analytical testing of samples in a cGMP compliant manner to service manufacturing and production. ESSENTIAL DUTIES AND RESPONSIBILITIES: 1. Perform routine physical testing of test samples. Report or request ...
Utility Qualification Engineer / Specialist
We are hiring Utility Qualification Engineer - experience directly related to qualification / validation within a pharmaceutical environment. Experience engineering utility systems. outlined by the FDA, ISO, EU and ICH. CV to firstname.lastname@example.org
Utility Qualification Engineer / Specialist: The candidate will assume a critical role in a highly motivated group within a leading contract manufacturing facility supporting the qualification of utility systems and ...
Sr. Home-based Regulatory Consultant, Pediatric Research
Are you someone with Regulatory Affairs expertise in PREA (Pediatric Research Equity Act) and have done writing of requests for pediatric waivers? CV to email@example.com MARKET RATE! OPEN DISCUSSION!
Sr. Home-based Regulatory Consultant, Pediatric Research Job Description Are you someone with Regulatory Affairs expertise in PREA (Pediatric Research Equity Act) and have done writing of requests for pediatric waivers? ...
Work from homelearn more
Senior Clinical Trial Associate
We are hiring Clinical Trial Associate in Princeton, NJ:5+ yrs pharma industry of Clinical trial support and Project Administration with a strong administrative background. Send CV to firstname.lastname@example.org for discussion
A Global Pharmaceutical company is looking for a Clinical Project Administrator/Clinical Trial Associate to join their CNS group. 5+ years of Clinical trial support and Project Administration experience within pharmaceutical ...
Sr. Pharmacovigilance System Analyst
Hiring Sr. Pharmacovigilance System Analyst in Greater Philadelphia areas with Pharma Drug Safety experience with database and query and reporting tools, SQL. Extensive analysis,reporting of drug safety,clinical trial data. CV to email@example.com
Reports to: Associate Director PV IT As Sr. Pharmacovigilance System Analyst you will be responsible for - Evaluating and implementing technical enhancements to support business processes, maintaining the business configuration ...
Regulatory Affairs Associate
We are hiring a Regulatory Affairs Associate in Princeton, NJ with 2-3 yrs experience in preparing INDs, NDAs, BLAs and EU submissions for US and EU. Knowledge of CMC, clinical,pre-clinical regulatory requirements. RAPS. Send CV to firstname.lastname@example.org
A leading global biopharmaceutical company is hiring a Regulatory Affairs Associate to assistant their regulatory operations. What do they want to accomplish - Assist Regulatory team in the coordination, compilation, ...
Sr. Clinical Data Associate/Manager
We are hiring Sr. CDM/CDA with 9 yrs of pharmaceutical experience in data cleaning/review in clinical trials including 6 yrs in managing the Data Mgmt processes and local to MD/DC/VA/DE areas. CV to email@example.com for discussion. OPEN RATE!
Job Description Qualified candidate must possess at least 6 years of Pharmaceutical industry Data Management experience and local to MD/DC/VA/DE areas or available to relocate to MD areas (close to ...
Washington, DClearn more
Sr. Drug Safety Scientist
HIRING for Sr. Clinical Safety in Greater Philadelphia - RN, BS with 3 years Pharma/CRO Drug Safety ;vaccine and medical device reporting and case review, extrapolation, ICSR narratives and causality assessment. Forward CV to firstname.lastname@example.org
We currently have several Drug Safety Specialist/Scientist openings with our clients, biopharmaceutical and Clinical Research Organization, located within 30 miles radius from Philadelphia, PA. *****There are 2 Sr. Drug Safety ...
Blue Bell, PAlearn more
Senior Clinical SAS Programmer
Sr. Clinical SAS Programmer in Greater Philadelphia - 6+ yts clinical programming/PK TLF programming experience; NDA submission - ISS programming and submission dataset development. PK submission datasets. Rate up to $100/hr. CV to email@example.com
Multiple Sr. Clinical SAS Programmer openings – long-term contract, contract-to-perm opportunities in Great Philadelphia areas. We are interested in H1B/EAD/GreenCard/US Citizen candidates. We are opened for W2 and 1099/corp-to-corp contract. ...
Drug Safety Specialist
Multiple Drug Safety openings in Princeton, NJ. PharmD or RN with 3-5 years industry drug safety experience. Forward CV to firstname.lastname@example.org
Drug Safety Specialist Processes serious adverse event reports, including triage, book-in, case preparation, submission and querying for follow-up information. Participates in query process, reconciliation process, submission process. Executes the Drug ...
Sr. Regional CRA
We are hiring Sr. Regional CRA in East and Mid-West Coast - requires 10 years pharmaceutical industry monitoring experience. CV to email@example.com for discussion.
We are hiring for Sr. Regional CRAs!!!!! Position Title: Sr. Regional CRA Type of the position: temp to hire or Long-term Contract assignment for Sr. CRA reside in Mid-West and ...
Sr. Regulatory Liaison (Director of Reg. Affairs) - Emerging Markets
Sr. Regulatory Liaison Consultant located in Exton, PA focus on Emerging Markets - Pay up to $150/hr. Please forward CV to firstname.lastname@example.org
Sr. Regulatory Liaison Consultant focus on Emerging Markets (anywhere else except U.S.) and provides global oversight, direction and leadership for all regulatory activities related to assigned products, encompassing investigational as ...
Exton, PAlearn more
Sr. Clinical Data Associate
We are hiring a Sr. CDA in MD/DC/VA areas with BS with 6+ years of pharma experience in data cleaning/review in clinical trials or 9 years of data management and EDC experience. Forward CV to email@example.com
Are you a Sr. 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 looking ...
Rockville, MDlearn more
Senior Home-based Medical Writer - Regulatory Writing
Home-based Sr. Medical Writer in greater Philadelphia areas. 10+ years of pharma industry regulatory writing experience required. forward CV to firstname.lastname@example.org for discussion
Field base Senior Medical Writer needed! Start ASAP! Flexible rate, Full time. Contract to Perm opportunity. Immediate opening for Senior Medical Writer to assist multiple therapeutic areas. Medical Writing team ...
Fort Washington, PAlearn more
We are looking for 2 strong Biostats located in MD/DC/VA areas; MS/PhD in Statistics/Biostatistics with 2 to 5+ years of pharma experience in Phase II/III studies as a Biostat. resume to email@example.com or #610-822-1256 for discussion.
We are looking for 2 strong Biostatisticians with a very stable work history for a leading Global Biopharmaceutical Company located in MD/DC/VA areas; The request below indicates MS/PhD in Statistics/Biostatistics ...
Rockville, MDlearn more