Phyllis Clark

Phyllis Clark Email and Phone Number

Study Management Associate III @ Srm Consulting Services LLC
sayreville, new jersey, united states
Phyllis Clark's Location
New Port Richey, Florida, United States, United States
Phyllis Clark's Contact Details

Phyllis Clark personal email

n/a
About Phyllis Clark

Over 28 years in the pharma, medical device and CRO industry with a strong skill set in project and clinical study management. Focus is on customer satisfaction and repeat business.

Phyllis Clark's Current Company Details
Srm Consulting Services LLC

Srm Consulting Services Llc

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Study Management Associate III
sayreville, new jersey, united states
Employees:
3
Phyllis Clark Work Experience Details
  • Srm Consulting Services Llc
    Project Manager
    Srm Consulting Services Llc Sep 2023 - Present
    Miami, Florida, United States
    Support submission of medical device 510k by providing input in meetings, providing information regarding the 510k filing, and manage CRA training. Responsibilities are flexible depending on assigned projects.
  • Syneos Health
    Project Manager
    Syneos Health May 2017 - Jun 2020
    North Chicago, Illinois, United States
    Support clinical study execution and identify issues that would potentially impact evaluable study data, ethical study conduct and ICH compliance. Lead study activities such as metric reports, creating newsletters and data trackers. Assist in the coordination of activities of cross-functional teams to ensure the initiation, conduct and completion of one or more clinical trials in the US and ex-US.
  • Randstad Life Sciences
    Contract Senior Medical Writer/Astellas
    Randstad Life Sciences Feb 2017 - Mar 2017
    Deerfield, Illinois
    Responsible for writing and editing clinical study reports, Investigator Brochures, Clinical Trial Results postings, annual reports, and other clinical regulatory documents across multiple therapeutic areas for Astellas Pharma US. Review clinical protocols, Statistical Analysis Plans, data tables and listings, and other clinical regulatory documents. Provides QC support and leads the process of critical review of clinical regulatory documents. Assists with training across functional areas.
  • Innovative Research Associates
    Clinical Project Director
    Innovative Research Associates May 2014 - Nov 2016
    Sharon Hill, Pa
    Responsible for growth of company, selecting vendors, coordinating monitoring visits, overseeing training of staff. Additional responsibilities include medical writing, quality control, co-monitoring, and development of protocols, informed consents and case report forms.
  • Novella Clinical, A Quintiles Company
    Clinical Trial Manager
    Novella Clinical, A Quintiles Company Nov 2013 - May 2014
    Morrisville, Nc
    Responsible for all activities related to implementation and execution of clinical studies that include working with Project Manager to define program targets for clinical monitoring staff. Assure needs of clinical sites are met by facilititating clinical monitoring processes. Coordinate and oversee daily operations of clinical monitoring team, manage project milestones and CRA performance.
  • Ram Consulting Group, Llc
    Contract Project Manager
    Ram Consulting Group, Llc Jul 2013 - Oct 2013
    Sharon Hill, Pa
    Responsible for creating protocols, inform consent forms and case report forms for new studies. Drafted white papers for publication.
  • Integrium
    Senior Project Leader
    Integrium Jun 2012 - Jun 2013
    Home Based
    Provide customer-focused leadership in managing multiple Phase 1 through Phase IV clinical research trials. Proposal development and bid defense for assigned RFPs.
  • Pharmanet/I3
    Senior Study Manager
    Pharmanet/I3 Jun 2009 - Jun 2012
    Supervise assigned projects including project team. Responsible for study budget, timelines, metrics.
  • Advanced Research Corporation
    Project Director
    Advanced Research Corporation Sep 2003 - Dec 2008
  • Purdue Pharma Lp
    Senior Clinical Trials Manager
    Purdue Pharma Lp 1997 - 2001

Phyllis Clark Skills

Clinical Research Project Management Clinical Monitoring Staff Management Budget Process Rfp Generation Medical Writing Quality Assurance Contract Negotiation Clinical Trials Ctms Edc Ich Gcp Therapeutic Areas Gcp Clinical Operations Protocol Regulatory Submissions Clinical Data Management Clinical Development Oracle Clinical Oncology Drug Development Regulatory Affairs Biotechnology Medical Devices Infectious Diseases Life Sciences Management Cro Pharmaceutical Industry Fda Sop Authoring

Phyllis Clark Education Details

Frequently Asked Questions about Phyllis Clark

What company does Phyllis Clark work for?

Phyllis Clark works for Srm Consulting Services Llc

What is Phyllis Clark's role at the current company?

Phyllis Clark's current role is Study Management Associate III.

What is Phyllis Clark's email address?

Phyllis Clark's email address is ph****@****lth.com

What schools did Phyllis Clark attend?

Phyllis Clark attended Long Island University, University At Buffalo.

What skills is Phyllis Clark known for?

Phyllis Clark has skills like Clinical Research, Project Management, Clinical Monitoring, Staff Management, Budget Process, Rfp Generation, Medical Writing, Quality Assurance, Contract Negotiation, Clinical Trials, Ctms, Edc.

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