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The Senior Meeting Planner will work with business partners and stakeholder for meetings and conventions to identify Pharmacyclics’ objectives and participation for company presence. Interact with and build relationships with internal business partners and senior leaders across the company. Have a working knowledge of project management methodologies, tools and templates and contributes to the dev...

Auto req ID 4590BR Job Posting Title: Director, Meetings & Conventions Person Type: Regular Posting Category Commercial Location: Tarrytown Job Summary and Essential Functions: Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of ser...

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, and a rare inflammatory condition and has product candidates in development in oth...

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, and a rare inflammatory condition and has product candidates in development in oth...

Job Title: Budget Project Manager - Medical Affairs and HEOR Working Arrangement:Onsite with large pharmaceutical company in Central NJ. Duties: Provide expertise and strategic leadership of key initiatives within the US GenMeds Medical Units and HEOR functions.Responsible to provide direction, oversight and coordination of complex activities within HEOR portfolio(s) and functions including budg...

Acts as lead statistical programmer for a project. -May participate in sub-team meetings as a representative of Statistical Programming group. -Provides consistency and quality assurance across various studies. -Independently identifies issues in the analysis plan from previous experience and knowledge. -Collaborates with Biostatisticians and Clinical Research Scientists on studies and helps d...

Summary:Ensures that Investigators are conducting clinical trials in accordance with international Regulatory and Ethical guidelines for Good Clinical Practices (GCP) and International Conference on Harmonization (ICH).Key Responsibilities: Performs Selection, Initiation, Monitoring and Closure Visits at Investigator Sites according to project schedule.Adheres to project guidelines and POI SOPs f...

Sr. Clinical Data Managers are needed to take on a lead role for their numerous ongoing cardiovascular, oncology and virology studies. This company is nationally recognized as an amazing place to work for, since they encourage professional success as well as personal growth. The benefits are highly competitive and suit professionals looking to take on secure roles within a stable company structure...

Essential Function The responsibility of a Sr. Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOPs. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when requ...

DOCS is actively seeking aRegional CRA with Oncology experience.May require up to 50% travel.Responsibilities include:-Coordinate monitor, reviews and generate queries of CRF's for clinical trials-Interface with, and assure training of investigators, center staff, trial monitors and clinical staff-Ensure adequate monitoring is conducted on all clinical trials including identification of issues and...

We are currently seeking a great CRA for a remote position with one of our best clients! Responsibilities: •Independently manage and monitor clinical trial sites •Proactively drive project success, including working closely with Project Managers to develop and implement enrollment strategies •Support the management and development of other CRAs •Attend and present at meetings and conferences,...

Are you looking for a new and exciting opportunity? Do you have experience in the pharmaceutical industry with clinical trials & project management experience?Well this Expert Clinical Manager position in East Hanover, NJ maybe the position for you. Responsible for all operational aspects of 1 or more OGD clinical trial(s) under the leadership of Clinical Trial Head (CTH). Support all scientific ...

Serves as primary contact point between the sponsor and investigational sites.Assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include site selection, pre-trial...

PHARMACEUTICALS BIOTECH SALES SPECIALIST REQUIREMENT #15-01153 RECRUITER: ERICA FLORES JOB LOCATION: SAN FRANCISCO, CA AUGUST 13, 2015 *** CANDIDATES MUST BE ABLE TO WORK ON OUR PAYROLL AS A W-2 *** *** Position is home-based to be located in San Francisco, CA area *** Basic Function: As members of the area sales team, individuals in this position are responsible for the promotion of the cl...

About The Opportunity:The Senior Clinical Data Manager coordinates and completes data management activities to ensure accuracy and consistency of clinical databases for subsequent analysis and reporting. This Is Your Day To Day:- Coordinate and complete data management activities to meet project timelines and communicate status to respective team members. - Perform coding review for adverse even...

About The Opportunity:Our client is based in the greater Philadelphia area. This position provides extensive visibility in various aspects of the clinical trial. This pharmaceutical company doesn't outsource any work or utilize any CRO's. Oncology experience isn't required, but preferred. This Is Your Day To Day:- Significant lead experience required. - Effectively designs and codes SAS programs ...

About The Opportunity:This is a great opportunity for someone looking to join an exciting pharmaceutical company in the greater Philadelphia area. Our client is highly successful and provides a team driven environment. With a strong pipeline and a significant revenue stream, the sky is the limit with this organization.If you enjoy working in a collaborative programming community, this is the perfe...

Serves as primary contact point between the CRO. sponsor and investigational sites. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilities include s...

RESPONSIBILITIES: Kforce has a client seeking a Biotech / Pharma - HTA Project Manager in Thousand Oaks, California (CA). Responsibilities: Apply project management principles and tools to internal HTA COE projects, projects may include database management with core HTA content, generating key reports and metrics, supporting internal workstreams, SharePoint management, etc Leverage internal wo...

Summary: The Clinical Team Leader (CTL) is responsible for the management of the Clinical portion of the studies. They will provide leadership and management to the Clinical Research Associates (CRA) and Lead Clinical Research Associates in global projects. The CTL will be responsible for direct communication and interaction with investigative site/monitors, managing the planning, implementation,...