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Joe Reynolds Email & Phone Number

Executive Director, Global Clinical Development at Merck
Location: Watertown, Massachusetts, United States 13 work roles 4 schools
1 work email found @c4therapeutics.com 2 phones found area 617 LinkedIn matched
✓ Verified Jun 2026 4 data sources Profile completeness 100%

Contact Signals · 1 work email · 2 phones

Work email j****@c4therapeutics.com
Direct phone (617) ***-****
LinkedIn Profile matched
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Current company
Role
Executive Director, Global Clinical Development
Location
Watertown, Massachusetts, United States

Who is Joe Reynolds? Overview

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Quick answer

Joe Reynolds is listed as Executive Director, Global Clinical Development at Merck, based in Watertown, Massachusetts, United States. AeroLeads shows a work email signal at c4therapeutics.com, phone signal with area code 617, and a matched LinkedIn profile for Joe Reynolds.

Joe Reynolds previously worked as Vice President, Portfolio Strategy and Development Program Leader at C4 Therapeutics, Inc. and Vice President, Development Program Lead at C4 Therapeutics, Inc.. Joe Reynolds holds Doctor Of Philosophy (Phd), Molecular Biology, Cell Biology And Biochemistry from Boston University.

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Email format at Merck

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{first_initial}{last}@c4therapeutics.com
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Profile bio

About Joe Reynolds

• Demonstrated pharmaceutical leader with experience across all stages of drug development (IND-enabling preclinical work through Phase 1, 2 and 3 studies through approval) spanning oncology, pulmonary disorders and rare diseases• Enterprise leader responsible for Program Management and Portfolio Strategy & Operations functions• Development program leader responsible for cross functional program teams• Advocated for, built, and led the Clinical Science department at Acceleron responsible for all Clinical Science activities across the Acceleron portfolio (including sotatercept for pulmonary arterial hypertension)• Experience with BLA and MAA filings leading to the approval of luspatercept-aamt (REBLOZYL®) for patients with myelodysplastic syndromes (MDS) and beta-thalassemia• Clinical leader responsible for the strategy, establishment, and execution of clinical development plans• Clinical trial experience spanning study start-up through study close out and CSR finalization• Demonstrated record of representing programs with internal and external stakeholders including collaborators (Celgene/Bristol Myers Squibb), senior/executive leadership, Board of Directors, regulatory authorities (FDA, EMA and PMDA), key opinion leaders, investigators, and patient groups

Listed skills include Drug Discovery, Clinical Development, Assay Development, Oncology, and 19 others.

Current workplace

Joe Reynolds's current company

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Merck
Merck
Executive Director, Global Clinical Development
Watertown, MA, US
AeroLeads page
13 roles

Joe Reynolds work experience

A career timeline built from the work history available for this profile.

Executive Director, Global Clinical Development

Watertown, MA, US

Vice President, Portfolio Strategy And Development Program Leader

Current

Watertown, MA, US

  • Lead for the Program Management and Portfolio Strategy & Operations functions
  • Development Program Lead for CFT1946 (in development for the treatment of BRAF V600 mutant solid tumors including NSCLC, melanoma and colorectal cancer) and CFT8634 (previously in development for the treatment of.
Sep 2023 - Present

Vice President, Development Program Lead

Watertown, MA, US

  • Development Program Lead for CFT8634 and CFT1946
May 2022 - Sep 2023

Senior Director, Global Clinical Lead, Pulmonary Fibrosis

Cambridge, MA, US

  • Global Clinical Lead of a cross functional team to establish and drive the Clinical Strategy and execution of Pulmonary Fibrosis Programs, including ACE-1334 a TGF-beta super-family ligand trap
  • Launch of the Phase 1b/2 trial in patients with Systemic Sclerosis (SSc)/SSc-associated interstitial lung disease (SSc-ILD)
  • Represent programs to leadership, internal and external stakeholders
  • Managed the Clinical Science function within Pulmonary Fibrosis to establish clinical and research collaborations to develop biomarker and translational science plans
Feb 2021 - Apr 2022

Senior Director, Clinical Lead Ace-1334

Cambridge, MA, US

  • Global Clinical Lead for the ACE-1334 program
  • Responsible for establishing the clinical strategy and the Clinical Development Plan for ACE-1334
  • Responsible the design of the first-in-patient Phase 1b study of ACE-1334 plus standard of care in participants with Systemic Sclerosis (SSc) and SSc-associated interstitial lung disease (SSc-ILD)
  • Recruited and managed external relationships including the program Steering Committee
  • Managed Clinical Scientists supporting ACE-1334
Jan 2020 - Apr 2022

Senior Director, Head Of Clinical Science

Cambridge, MA, US

  • Head of Clinical Science at Acceleron Pharma managing a team of 5 Clinical Scientists providing support to the companies portfolio
  • In collaboration with Celgene/BMS, content author and team member for the submission of the BLA for REBLOZYL (luspatercept-aamt) leading to FDA approval for patients with MDS and beta-thalassemia
  • In collaboration with Celgene/BMS, content author and team member for the submission and approval of luspatercept-aamt for Marketing Authorisation by the EMA
  • Luspatercept subject matter expert supporting Commercial and Medical Affairs activities for the REBLOZYL launch
  • Subject matter expert for luspatercept Clinical Development in response to Health Authority questions
  • Clinical Scientist supporting the Clinical Development of luspatercept including the Phase 2 and Phase 3 studies (in collaboration with Celgene/BMS) across multiple indications
Feb 2018 - Feb 2021

Director, Clinical Science

Cambridge, MA, US

  • Director of Clinical Science focusing on:
  • The development of luspatercept for myelodysplastic syndromes (MDS) and beta-thalassemia
  • The development of sotatercept for pulmonary arterial hypertension (PAH)
Jan 2017 - Jan 2018

Associate Director, Clinical Science And Drug Development

Cambridge, Massachusetts, US

  • Associate Director of Clinical Science and Drug Development for MM-302 focusing on:
  • Medical monitoring of ongoing studies
  • Ensuring maintenance of clinical study conduct
  • Overseeing all program-specific clinical science activities
  • Relationship building with clinical investigators and key opinion leaders (KOLs)
  • Global long-term drug development strategy
Dec 2014 - Jan 2017

Principal Clinical Scientist

Cambridge, Massachusetts, US

  • Principal Clinical Scientist for MM-302 focusing on:
  • Medical monitoring
  • Development of study safety documents
  • Development of the strategy for investigator and KOL identification and study recruitment
  • Preparation of a briefing documents for regulatory interactions
  • Representing the program at regulatory interactions
Dec 2013 - Dec 2014

Senior Clinical Scientist

Cambridge, Massachusetts, US

  • Senior Clinical Scientist for MM-302 (a HER2-targeted PEGylated liposomal doxorubicin) focusing on:
  • Clinical development
  • Oncology clinical trial design, feasibility and implementation
  • Synopsis and clinical protocol writing
  • Analysis and interpretation of clinical data
  • Ensuring maintenance of clinical study conduct
Nov 2012 - Dec 2013

Senior Scientist

Cambridge, Massachusetts, US

  • Senior Scientist for MM-302 (a HER2-targeted PEGylated liposomal doxorubicin) focusing on:
  • Drug discovery
  • Early stage clinical development
  • Stem cell-derived cardiac models and their use as a preclinical toxicity screening platform
  • High content microscopy (HCM) and quantitative analysis
  • Deconvolution microscopy
Jan 2011 - Nov 2012

Scientist

Cambridge, Massachusetts, US

  • Scientist for an early stage drug discovery project and MM-302 (a HER2-targeted PEGylated liposomal doxorubicin) focusing on:
  • Early stage preclinical drug discovery
  • Therapeutic target identification and validation
  • IND enabling studies
  • Drug mechanism of action
  • Microscopy
Jul 2008 - Jan 2011

Call/Volunteer Fire Fighter

Boxford Fire Department
Jun 2012 - Jul 2014
4 education records

Joe Reynolds education

Doctor Of Philosophy (Phd), Molecular Biology, Cell Biology And Biochemistry

Boston University

Master Of Arts (M.A.), Molecular Biology, Cell Biology, & Biochemistry

Boston University

Bachelor Of Science (B.S.), Biochemistry

Bates College

Education record

Winnacunnet High School
FAQ

Frequently asked questions about Joe Reynolds

Quick answers generated from the profile data available on this page.

What company does Joe Reynolds work for?

Joe Reynolds works for Merck.

What is Joe Reynolds's role at Merck?

Joe Reynolds is listed as Executive Director, Global Clinical Development at Merck.

What is Joe Reynolds's email address?

AeroLeads has found 1 work email signal at @c4therapeutics.com for Joe Reynolds at Merck.

What is Joe Reynolds's phone number?

AeroLeads has found 2 phone signal(s) with area code 617 for Joe Reynolds at Merck.

Where is Joe Reynolds based?

Joe Reynolds is based in Watertown, Massachusetts, United States while working with Merck.

What companies has Joe Reynolds worked for?

Joe Reynolds has worked for Merck, C4 Therapeutics, Inc., Acceleron Pharma, Merrimack, and Boxford Fire Department.

How can I contact Joe Reynolds?

You can use AeroLeads to view verified contact signals for Joe Reynolds at Merck, including work email, phone, and LinkedIn data when available.

What schools did Joe Reynolds attend?

Joe Reynolds holds Doctor Of Philosophy (Phd), Molecular Biology, Cell Biology And Biochemistry from Boston University.

What skills is Joe Reynolds known for?

Joe Reynolds is listed with skills including Drug Discovery, Clinical Development, Assay Development, Oncology, Drug Development, Cell Culture, Elisa, and Molecular Biology.

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