Employment Opportunities

Impact is always looking for exceptional talent — for individuals committed to excellence in clinical research. If you are looking for a challenging opportunity with career growth potential in clinical research, submit your information below.

Medical Writer – Consultant

Functions/Responsibilities

• Oversees the development of protocols, Informed Consent Forms, and amendments. Including managing project timelines, drafting, editing, coordinating review cycles, adjudicating reviewer comments, and overseeing publishing,  and finalization
• Acts as a key strategic thinking partner for team members on protocol development and the above deliverables
• Actively keeps team members apprised of projects and timelines

Who you are

• 2 years or more years of medical writing and/or clinical project management experience, preferably in the biotech/Pharmaceutical industry
• Masters or PhD degree in the biological sciences or liberal arts preferred or equivalent experience

Capabilities

• Superb written and oral communication skills, with a proven ability to communicate effectively with all levels in the organization
• Demonstrated experience in clinical and nonclinical document preparation and finalization
• Strong project management and team facilitation skills
• Team player with demonstrated strong interpersonal skills and ability to build effective working relationships throughout all levels of the organization
• Strong analytical and problem-solving skills, paired with strong partnering and performance consulting skills
• Ability to work independently and as part of a team
• Strong planning and organizational skills, including ability to prioritize and organize high volume workflow ensuring attention to detail, and highest level of accuracy within required timeframe

Please submit a simple text resume below. Thank you!