Offer summary

Qualifications:

Bachelor's degree in life sciences or related field., Proven experience in medical writing, preferably in a pharmaceutical or biotech setting., Strong understanding of clinical research and regulatory requirements., Excellent communication and organizational skills..

Key responsibilities:

Develop and write clinical study protocols, reports, and other regulatory documents.

Collaborate with cross-functional teams to ensure accuracy and compliance of documents.

Review and edit documents for clarity, consistency, and adherence to guidelines.

Participate in meetings with clients and stakeholders to discuss project requirements.

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. We bring together a talented team of professionals with a deep understanding of patient and physician behaviors and market dynamics. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. Syneos Health supports a diverse, equitable and inclusive culture that cares for colleagues, customers, patients, communities and the environment.

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