Research Associate III
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Actalent
Lexington, MA (In Person)
$126,880 Salary, Full-Time
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Job Description
Description Our East Coast Global Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R D community based on collaboration, partnerships, and cutting-edge research across multiple innovative modalities and therapeutic areas. Our East Coast Global Development Hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients. We recognize that improving human health starts here and that patients rely on us. We're changing lives for a living. Are you ready to make a difference?
Additional Skills & Qualifications Essential Functions:
- Hands-on in vivo experimental efforts
- Designs and conducts in vivo research studies
- Independently leads the development and implementation of assays to support research projects
- Interpret and properly document experimental data
- Ensures data integrity and documentation through maintenance of laboratory notebooks and ensuring data and results are entered into the electronic notebook in a timely man-ner
- Point of contact person for specific in vivo platform and methodologies.
- Collaborative Teamwork and develop synergy with technical and scientific experts within the team.
- Works in a team-focused environment to ensure progress of global research projects
- Works with team to ensure better practice sharing and implementation within the lab
- Supports business goals, shares learnings, knowledge and skills, and cross-functional teamwork
- be a team player and regularly provides assistance to other technical staff
- Scientific input & guidance
- Independently executes experiments and performs data analyses of moderate complexity
- Correctly interprets data and make recommendations for next steps
- Responsible for developing, optimizing & drafting protocols for methods of moderate complexity with limited input from supervisor
- Contributes to formal study reports & study protocol drafting & review
- Supports development and management of research protocols in support of multiple drug discovery efforts
- Presents findings at the scientist, department, and site-level
- Manages personal experimental timelines
- Will require weekend tasks which are a shared and divided responsibility among the team
Physical Requirements:
0-10% overnight travel required. Ability to lift 50lbs.Qualifications:
- High School Diploma with 10+ years' experience required.
- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Lexington,MA.
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