Clinical Research Coordinator

Acceleron Pharma

Cambridge, MA, US
  • Job Type: Full-Time
  • Function: Clinical Research
  • Post Date: 04/01/2021
  • Website: acceleronpharma.com
  • Company Address: 128 Sidney Street, Cambridge, MA, 02139

About Acceleron Pharma

Acceleron is a biopharmaceutical company dedicated to the discovery, development, and commercialization of therapeutics to treat serious and rare diseases. The Company's leadership in the understanding of TGF-beta superfamily biology and protein engineering generates innovative compounds that engage the body's ability to regulate cellular growth and repair.

Job Description

The Clinical Research Coordinator will be an individual responsible for supporting Clinical Operations Team members with project-specific support related to the conduct of clinical trials activities. As a Clinical Research Coordinator, you will assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support.

 

What will you be doing?

  • Provides Clinical Operations Team members with administrative and project-specific support related to the conduct of clinical trials
  • Responsible for maintaining clinical study trackers
  • Adheres to Clinical Standard Operating Procedures and Good Clinical Practice ICH Guidelines
  • Helps coordinate and contributes to reviewing study documents
  • Helps coordinate project team meetings, agenda & minutes
  • Helps coordinate distribution of clinical trial supplies
  • Assists in supporting review of clinical trial data
  • Assists with auditing and maintaining TMF
  • Verifies and tracks invoices
  • Tracks the collection, shipment, and analysis of clinical samples
  • Attending study team and department meetings while assisting with meeting logistics (scheduling, room and equipment set up, attendance tracking), agenda preparation, draft meeting minutes, and collating materials for meetings
  • Developing an understanding of clinical trial research through exposure to research protocols, the drug development process, clinical meetings, Company Standard Operating Procedures (SOPs), and Food and Drug Administration (FDA) guidelines as related to Good Clinical Practices (GCP)

 

What are we looking for?

  • Bachelor’s Degree or equivalent experience
  • 1-2 years of experience working in academic study center, pharmaceutical/biotechnology or CRO organization
  • Proficient in computer technology used in an office environment (Microsoft Word, Excel, and PowerPoint)
  • Ability to work independently and excellent written communication, oral communication, and organizational skills are required
  • Ability to work on multiple clinical projects and manage priorities effectively
  • Strong interest in clinical trials and initiative to learn and participate in projects of increasing responsibility
  • Minimal travel required

 

How will you grow with us?

As a member of the Clinical Operations team during this time of dynamic growth, you will directly impact the success of multiple programs.  This role provides a tremendous opportunity to gain experience in clinical development in a dynamic, fast-paced, and innovative company.  Join our team and help us in our mission of transforming the lives of patients!

 

Acceleron is a biopharmaceutical company dedicated to the discovery, development, and commercialization of therapeutics to treat serious and rare diseases. Acceleron’s leadership in the understanding of TGF-beta superfamily biology and protein engineering generates innovative compounds that engage the body's ability to regulate cellular growth and repair. Acceleron focuses its research, development, and commercialization efforts in pulmonary and hematologic diseases. In pulmonary, Acceleron is developing sotatercept for the treatment of pulmonary arterial hypertension (PAH), having reported positive topline results of the PULSAR Phase 2 trial. The Company is currently planning multiple Phase 3 trials with the potential to support its long-term vision of establishing sotatercept as a backbone therapy for patients with PAH at all stages of the disease. Acceleron is also investigating the potential of its early-stage pulmonary candidate, ACE-1334, which it plans to advance into a Phase 1b/2 trial in systemic sclerosis-associated interstitial lung disease (SSc-ILD) next year. In hematology, REBLOZYL® (luspatercept-aamt) is the first and only erythroid maturation agent approved in the United States, Europe, and Canada for the treatment of anemia in certain blood disorders. REBLOZYL is part of a global collaboration partnership with Bristol Myers Squibb. The Companies co-promote REBLOZYL in the United States and are also developing luspatercept for the treatment of anemia in patient populations of myelodysplastic syndromes, beta-thalassemia, and myelofibrosis. For more information, please visit www.acceleronpharma.com. Follow Acceleron on Social Media: @AcceleronPharma and LinkedIn.

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This company does NOT accept candidates from outside recruiting firms. Agency contacts are not welcome.