Clinical Trial Associate
Full Time
Cambridge, MA 02142
$68,000 - $85,000 a year
Posted
Job description
The Clinical Trial Associate, Global Clinical Operations is an early career professional who supports in the planning, execution, and management of clinical trials.
Primary Responsibilities Include:
- Coordinates and tracks the distribution and subsequent retrieval of clinical documents, including but not limited to protocols, protocol amendments, IBs, ICF’s, monitoring visit reports, etc.
- Supports maintenance of inspection-ready Trial Master File (TMF) according to ICH-GCP and company SOPs
- May perform quality checks on the study TMF with oversight of study COL
- Assists in the preparation of study related documents, i.e., ICF, clinical trial tools and templates, etc.
- May coordinate and track clinical trial equipment and supplies
- May review and track vendor invoices against contracts with oversight of study COL
- Coordinates and tracks administrative aspects of contract execution and PO generation
- Supports the trial team to produce and distribute study newsletters
- Supports collection and updating of clinical trial insurance
- Assists with various supportive trial activities, i.e., meeting management including agenda distribution and minute taking, internal database maintenance, study team contact list, etc.
- May support additional ad-hoc activities as agreed with the study COL
Desired Education and Skills:
- Strong computer skills including knowledge of Excel, Word, PowerPoint and Outlook
- Solid understanding of the responsibilities and needs of other functions in a clinical trial
- Proven ability to work independently and effectively handle multiple priorities in a fast-paced environment
- Ability to maintain confidentiality of proprietary information
- A team player that takes initiative
- Excellent interpersonal skills, strong organizational skills, and effective communication across all levels within an organization
- Proficient written and verbal communication skills
- Position may require some travel
- Bachelor’s degree in life sciences or healthcare related field
- 2+ years’ experience in a clinical research related position
#LI-CK1
#LI-Hybrid
This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time.
The targeted salary range for this position is $68,000 - $85,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.
Candidates must be authorized to work in the U.S.
Sarepta Therapeutics offers a competitive compensation and benefit package.
Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.
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