ACAD
38.03
-0.64
-1.66%
AEMD
0.196
-0.01
-4.6341%
APRI
1.77
-0.01
-0.56%
ARNA
4.64
-0.02
-0.43%
ATEC
1.43
+0.02
+1.42%
CNAT
6.43
-0.22
-3.31%
CRXM
0.35
+0.06
+20.69%
CYTX
1.11
-0.03
-2.63%
DXCM
67.4
-0.53
-0.78%
GNMK
10.86
-2.02
-15.68%
HALO
15.3
-0.22
-1.42%
ILMN
191.16
-1.86
-0.96%
INNV
0.15
0.00
0.00%
INO
10.04
-0.28
-2.76%
ISCO
0.057
-0.001
-0.870%
ISIS
65.33
-0.98
-1.48%
LGND
85.85
-1
-1.15%
LPTN
2.26
+0.03
+1.35%
MBVX
3.55
+0.05
+1.43%
MEIP
2.12
0.00
0.00%
MNOV
4.45
-0.51
-10.28%
MRTX
27.59
-0.21
-0.76%
MSTX
0.472
-0.009
-1.871%
NBIX
42.49
-1.12
-2.57%
NUVA
41.55
-1.18
-2.76%
ONCS
0.31
0.00
-1.59%
ONVO
4.56
-0.16
-3.39%
OREX
7.54
-0.26
-3.33%
OTIC
31.86
-0.52
-1.61%
QDEL
23.7
-0.9
-3.66%
RCPT
167.38
-0.59
-0.35%
RGLS
17.3
+0.12
+0.70%
RMD
71.88
-0.37
-0.51%
SCIE
0.025
-0.002
-7.063%
SPHS
0.81
-0.05
-5.81%
SRNE
11.31
+0.16
+1.43%
TROV
8.53
+1.43
+20.14%
VICL
0.94
-0.01
-1.05%
VOLC
17.99
0.00
0.00%
ZGNX
1.58
-0.02
-1.25%
ACAD
38.03
-0.64
-1.66%
AEMD
0.196
-0.01
-4.6341%
APRI
1.77
-0.01
-0.56%
ARNA
4.64
-0.02
-0.43%
ATEC
1.43
+0.02
+1.42%
CNAT
6.43
-0.22
-3.31%
CRXM
0.35
+0.06
+20.69%
CYTX
1.11
-0.03
-2.63%
DXCM
67.4
-0.53
-0.78%
GNMK
10.86
-2.02
-15.68%
HALO
15.3
-0.22
-1.42%
ILMN
191.16
-1.86
-0.96%
INNV
0.15
0.00
0.00%
INO
10.04
-0.28
-2.76%
ISCO
0.057
-0.001
-0.870%
ISIS
65.33
-0.98
-1.48%
LGND
85.85
-1
-1.15%
LPTN
2.26
+0.03
+1.35%
MBVX
3.55
+0.05
+1.43%
MEIP
2.12
0.00
0.00%
MNOV
4.45
-0.51
-10.28%
MRTX
27.59
-0.21
-0.76%
MSTX
0.472
-0.009
-1.871%
NBIX
42.49
-1.12
-2.57%
NUVA
41.55
-1.18
-2.76%
ONCS
0.31
0.00
-1.59%
ONVO
4.56
-0.16
-3.39%
OREX
7.54
-0.26
-3.33%
OTIC
31.86
-0.52
-1.61%
QDEL
23.7
-0.9
-3.66%
RCPT
167.38
-0.59
-0.35%
RGLS
17.3
+0.12
+0.70%
RMD
71.88
-0.37
-0.51%
SCIE
0.025
-0.002
-7.063%
SPHS
0.81
-0.05
-5.81%
SRNE
11.31
+0.16
+1.43%
TROV
8.53
+1.43
+20.14%
VICL
0.94
-0.01
-1.05%
VOLC
17.99
0.00
0.00%
ZGNX
1.58
-0.02
-1.25%
Home » Archive by Category

San Diego Biotech Jobs

San Diego, La Jolla, and Carlsbad biotechnology and life science jobs, updated with at least 5 new positions per day. Browse jobs, submit, get email updates.

Executive Assistant (Biotech/Pharma) at Streffco Consultants (Washington, DC)

February 27, 2015 – 11:49 pm

Title: Executive Assistant I, Global Regulatory Policy Job ID: 6413 Industry: Biotech/Pharmaceutical Location: Washington, DC Duration: 1 Year Contract Pay Rate Range: Depends on Experience (W-2 all inclusive rate) Job Details: We are…

Clinical Trial Associate (Study Start Up)

February 27, 2015 – 10:00 pm

Details: Alkermes is a leader in innovative medicines that address the unmet needs and challenges of people living with debilitating diseases. As a fully integrated global biopharmaceutical company, Alkermes applies our scientific expertise, proprietary technologies, and global resources to develop products that are designed to make a meaningful difference in the way patients manage their disease. Our track record for successful drug development is evident from the more than 20 marketed drugs that use our proprietary technologies, and perhaps most clearly exemplified by the five key commercial products propelling our growth. These are breakthrough products in major disease areas, such as schizophrenia, addiction, and multiple sclerosis. Alkermes is in an exciting phase of growth that few biotechnology companies achieve, with our diversified portfolio of commercial products and an exciting late-stage pipeline. We are moving ahead with global capabilities, an established approach to innovation, world-class manufacturing, financial strength, and our experienced and dedicated people. Description: Position Summary: Project support: Responsible for coordination, logistics, tracking and administrative tasks in support of clinical study start up. Operational support: Responsible for special projects supporting departmental operations. Duties and Responsibilities: Clinical project team member: works closely with the Associate Director, Study Start Up and is responsible for coordination, logistics, tracking and administrative tasks in support of clinical study start up. Supports and tracks study start up status and metrics, for assigned clinical projects. Responsible for data entry into Clinical Trial Management Systems, including Investigator databases, and/or other systems as required. Supports and/or tracks external access rights to Clinical Trial Management Systems. Interacts with CROs, vendors, clinical sites, monitors and other external partners to provide information and resolution for specific requests and issues. In conjunction with clinical operations team, manages and tracks clinical and non-clinical supplies required for distribution during study start up. In conjunction with clinical project team, responsible for review of regulatory documents and verification of other items required to initiate drug shipment. Assists with and/or responsible for agendas and meeting minutes for clinical start up meetings. Assists with logistics coordination for investigator meetings and external vendor meetings, as needed. Responsible for routing, tracking, and coordinating site and CRO/vendor Confidential Disclosure Agreements (CDAs) and contracts as directed. Responsible for review of site- and/or country-specific clinical trial budgets, with supervision by Associate Director, Study Start Up and/or clinical project team. Research country-specific clinical trial laws and regulations, upon request, in order to provide resources or information to Associate Director Study Start up and/or clinical project team. Coordinate with clinical operations project team on set-up of Trial Master File systems. Responsible for special projects supporting operations/departmental initiatives such as ClinicalTrials.gov, SOPs, GCP, process enhancements, outsourcing, Sunshine Act etc. Education/Skills and Experience Requirements for CTA level: Bachelor’s degree or equivalent undergraduate degree with science or healthcare experience preferred Experience: 1-2 years clinical research experience in a pharmaceutical/biotech, CRO setting preferred Basic knowledge and understanding of GCP/ICH Guidelines for conducting clinical trials Strong interpersonal, organizational, and multi-tasking skills Excellent attention to detail and problem solving skills Self-motivated and displays initiative Adaptable to changing priorities, excels in fast-paced environment Perform job duties with minimal supervision and guidance Ability to work effectively work in a team setting Education/Skills and Experience Requirements for Sr. CTA level: Bachelor’s degree or equivalent undergraduate degree with science or healthcare experience Experience: minimum 5 years clinical research experience in a pharmaceutical/biotech, CRO setting Solid knowledge and understanding of GCP/ICH Guidelines for conducting clinical trials Strong interpersonal, organizational, and multi-tasking skills Excellent attention to detail and problem solving skills Self-motivated and displays initiative Adaptable to changing priorities, excels in fast-paced environment Perform job duties with minimal supervision and guidance Ability to work effectively work in a team setting Physical Demands and Work Environment: ● Travel domestic and international – minimal 0-5% Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.

Hematology Translational Research – Senior Scientist Job – Johnson & Johnson – Spring House, PA

February 27, 2015 – 9:55 pm

In Molecular Biology or related field with at least 3 experience of applicable translational, biomarker, program management, clinical trial and/or research…
From Johnson & Johnson Family of Companies – 28 Feb 2015 04:55:42 GMT

Senior Director of Regulatory Affairs – Bootstrap Incubation – San Diego, CA

February 27, 2015 – 9:32 pm

Scientific degree (chemistry or biology) plus a minimum 10-15 years’ experience in a clinical stage cell therapy, pharmaceutical or biotechnology company;…
From Bootstrap Incubation – 28 Feb 2015 04:32:29 GMT
– View all San Diego jobs

Senior Director of Regulatory Affairs – Bootstrap Incubation – San Diego, CA

February 27, 2015 – 9:32 pm

Scientific degree (chemistry or biology) plus a minimum 10-15 years’ experience in a clinical stage cell therapy, pharmaceutical or biotechnology company;…
From Bootstrap Incubation – 28 Feb 2015 04:32:29 GMT
– View all San Diego jobs

Biotech Spectroscopy Technician at Lab Support (Pittsburgh, PA)

February 27, 2015 – 9:16 pm

Lab Support is currently working with one of our Biotech clients to fill a Mass Spectrometry Laboratory Technician role. -Tuesday-Saturday -Must be open to some odd hours. Responsibilities: Prepares specimens for analysis and run mass…

Corporate Recruiter – Permanent within Pharma/biotech Sector (Large Madison Employer) at Pharmaceutical Product Development (Middleton, WI)

February 27, 2015 – 8:40 pm

The Corporate Recruiter is responsible for high volume sourcing, recruiting, and referring of best-qualified candidates for vacant scientific professional positions in an efficient and fiscally responsible manner. Keeps abreast of industry…

Associate Director/Director, Data Management – Halozyme Therapeutics, Inc. – San Diego, CA

February 27, 2015 – 7:39 pm

Knowledge of the pharmaceutical, biotechnology, biomedical, and/or clinical research industry. The Associate Director/Director, Data Management, is responsible…
From DeviceSpace.com – 28 Feb 2015 02:39:32 GMT
– View all San D…

Quality Assurance / Administration (La Jolla)

February 27, 2015 – 7:29 pm

Bio-Edge, Inc. is a small Biomedical-Polymer chemistry company located in La Jolla, CA, specializing in R&D and laboratory scale manufacturing since 1993.
This position is responsible for the formation and maintenance of the Quality System for new a […]

Research Technician (Temporary) (Sorrento Mesa)

February 27, 2015 – 7:20 pm

At ACON labs, we are making a difference in medical care by offering medical devices for diagnosing a variety of conditions. In addition, we are able to streamline and reduce costs for the physician and/or patient directly.
We are seeking a temporar […