nick wilkening

senior associate, program management

About

Senior Associate, Program Management at Heron Therapeutics, Inc.

Country

united states

City

san diego

Industry

biotechnology

Skill

microsoft office, customer service, microsoft excel, management, microsoft word, powerpoint, public speaking, research, leadership, microsoft project, spotfire, document management, pharmaceutical industry

Experience

pharmacovigilance associate

heron therapeutics, inc.

2017-1 - Present · 9 yrs 9 mos

patent intern

ardea biosciences, inc., a member of the astrazeneca group

2015-6 - 2015-9 · 4 mos

Maintained the company patent docket under the supervision of a patent agent. Responsible for organization, archival, and assembly of patent files. Supported patent filing by drafting claim responses and reviewing data. Supported a patent agent with clinical trial transparency activities.

tour guide

hike bike kayak sports

2014-7 - 2015-8 · 1 yr 2 mos

Guided clients on kayak and snorkeling tours of the Matlahuayl State Marine Reserve, La Jolla, CA. Instructed groups of 10 or more clients on how to safely maneuver their kayaks while exploring various ecosystems in the reserve. Informed clients of the various state and federal laws that provide boundaries and protections for marine species within the reserve. Entertained clients with factual knowledge while embellishing with local La Jolla lore.

tour guide

rivers end rafting

2012-6 - 2012-9 · 4 mos

program management associate

heron therapeutics, inc.

2018-1 - Present · 8 yrs 9 mos

pharmacovigilance project assistant

ardea biosciences, inc., a member of the astrazeneca group

2015-10 - 2016-12 · 1 yr 3 mos

Co-managed the first Periodic Benefit-Risk Evaluation Report (PBRER) at Ardea Biosciences. Oversaw quality control efforts during the migration of a clinical safety database to a post-marketing capable global safety database. Developed expertise in safety systems to investigate status of post-marketing cases and to perform database queries for reconciliation purposes. Monitored serious adverse events (SAEs) in a global safety database and improved the quality control process by designing custom line listings. Supported the Safety Management Team with data analysis of large adverse event data files.